The present invention relates to molecular complexes of the herbicide pinoxaden. In particular, the invention relates to molecular complexes comprising pinoxaden with carboxylic acids, and to herbicidal compositions comprising such molecular complexes.

Pinoxaden has the chemical name [8-(2,6-diethyl-4-methylphenyl)-7-oxo-1,2,4,5- tetrahydropyrazolo[1,2-d][1,4,5]oxadiazepin-9-yl] 2,2-dimethylpropanoate and the chemical structure as illustrated below:

Definitions

The term “about” or “approximately” means an acceptable error for a particular value as determined by a person of ordinary skill in the art, which depends in part on how the value is measured or determined. In certain embodiments, the term “about” or “approximately” means within 1 , 2, 3 or 4 standard deviations. In certain embodiments, the term “about” or “approximately” means within 30%, 25%, 20%, 15%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of a given value or range. In certain embodiments and with reference to X-ray powder diffraction two-theta peaks, the terms “about” or “approximately” means within ± 0.2 ° 2q.

“Alkyl” refers to a straight-chain or branched saturated hydrocarbon group. In certain embodiments, the alkyl group may have from 1-20 carbon atoms, in certain embodiments from 1-15 carbon atoms, in certain embodiments, 1-8 carbon atoms. The alkyl group may be unsubstituted. Alternatively, the alkyl group may be substituted. Unless otherwise specified, the alkyl group may be attached at any suitable carbon atom and, if substituted, may be substituted at any suitable atom. Typical alkyl groups include but are not limited to methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl and the like.

The term “ambient temperature” means one or more room temperatures between about 15 °C to about 30 °C, such as about 15 °C to about 25 °C.

“Aryl” refers to an aromatic carbocyclic group. The aryl group may have a single ring or multiple condensed rings. In certain embodiments, the aryl group can have from 6-20 carbon atoms, in certain embodiments from 6-15 carbon atoms, in certain embodiments, 6-12 carbon atoms. The aryl group may be unsubstituted. Alternatively, the aryl group may be substituted. Unless otherwise specified, the aryl group may be attached at any suitable carbon atom and, if substituted, may be substituted at any suitable atom. Examples of aryl groups include, but are not limited to, phenyl, naphthyl, anthracenyl and the like.

“Arylalkyl” refers to an optionally substituted group of the formula aryl-alkyl-, where aryl and alkyl are as defined above.

The term “crystalline” and related terms used herein, when used to describe a compound, substance, modification, material, component or product, unless otherwise specified, means that the compound, substance, modification, material, component or product is substantially crystalline as determined by X- ray diffraction. See, e.g., Remington: The Science and Practice of Pharmacy, 21st edition, Lippincott, Williams and Wilkins, Baltimore, Md. (2005); The United States Pharmacopeia, 23rd ed., 1843-1844 (1995).

“Halo”, “hal” or “halide” refers to -F, -Cl, -Br and -I.

The term “molecular complex” is used to denote a crystalline material composed of two or more different components which has a defined single-phase crystal structure. The components are held together by non-covalent bonding, such as hydrogen bonding, ionic bonding, van der Waals interactions, p-p interactions, etc. The term “molecular complex” includes salts, co-crystals and salt/co-crystal hybrids. In one embodiment, the molecular complex is a salt. In another embodiment, the molecular complex is a co-crystal. In another embodiment, the molecular complex is a salt/co-crystal hybrid.

Without wishing to be bound by theory, it is believed that when the molecular complex is a co-crystal, the co-crystal demonstrates improved physiochemical properties, such as crystallinity, solubility properties and/or modified melting points. In certain embodiments, the melting point of the molecular complex may be higher than the melting point of pinoxaden itself. In this instance, a higher melting point may be of benefit in the preparation of, for example, a suspension concentrate formulation of the molecular complex. In certain embodiments, the melting point of the molecular complex may be lower than the melting point of pinoxaden itself. In this instance, a lower melting point may be of benefit in the preparation of, for example, an encapsulated formulation of the molecular complex or liquid formulation of the molecular complex.

The molecular complexes may be distinguished from mixtures of pinoxaden and the selected molecular complex former, such as a carboxylic acid, by standard analytical means which are well known to those skilled in the art, for example X-ray powder diffraction (XRPD), single crystal X-ray diffraction, or differential scanning calorimetry (DSC). The molar ratio of the components of the molecular complex may be determined using, for example, HPLC or ¹ H-NMR. The term “overnight” refers to the period of time between the end of one working day to the subsequent working day in which a time frame of about 12 to about 18 hours has elapsed between the end of one procedural step and the instigation of the following step in a procedure.

“Slurry” means a heterogeneous mixture of at least a portion of the molecular complex in one or more solvents. “Slurry” therefore includes a mixture of molecular complex which is partially present as a solid, as well as being partially dissolved in the one or more solvents.

“Substituted” refers to a group in which one or more hydrogen atoms are each independently replaced with substituents (e.g. 1 , 2, 3, 4, 5 or more) which may be the same or different. The group may be substituted with one or more substituents up to the limitations imposed by stability and the rules of valence. The substituents are selected such that they do not adversely affect the molecular complexes. Examples of substituents include but are not limited to -halo, -CF ₃ , -R ^a , -O-R ^a , -S-R ^a , -NR ^a R ^b , -CN, - C(O)-R ^a , -COOR ^a , and -CONR ^a R ^b , preferably -halo, - CF ₃ , -R ^a , -O-R ^a , -NR ^a R ^b , -COOR ^a , and -CONR ^a R ^b . R ^a and R ^b are independently selected from the groups consisting of H, alkyl, aryl, and arylalkyl, and wherein R ^a and R ^b may be unsubstituted or further substituted as defined herein.

Description of the Figures

Figure 1 shows a representative x-ray diffraction pattern (XRPD) of the molecular complex of Example 2.

Figure 2 shows a representative differential scanning calorimetry (DSC) curve for the molecular complex of Example 2.

Figure 3 shows a representative x-ray diffraction pattern (XRPD) of the molecular complex of Example 3.

Figure 4 shows a representative differential scanning calorimetry (DSC) curve for the molecular complex of Example 3.

Figure 5 shows a representative x-ray diffraction pattern (XRPD) of the molecular complex of Example 5.

Figure 6 shows a representative differential scanning calorimetry (DSC) curve for the molecular complex of Example 5.

Figure 7 shows a representative x-ray diffraction pattern (XRPD) of the molecular complex of Example 7. Figure 8 shows a representative differential scanning calorimetry (DSC) curve for the molecular complex of Example 7.

Description of the Invention

It is an object of the present invention to provide a crystalline molecular complex of the herbicide pinoxaden and a carboxylic acid. In certain embodiments, the crystalline molecular complex is purifiable. In certain embodiments, the crystalline molecular complex facilitates obtaining pinoxaden in an improved purity. In certain embodiments, the crystalline molecular complex is stable. In certain embodiments, the crystalline molecular complex is easy to isolate and handle. In certain embodiments, the process for preparing the crystalline molecular complex is scalable. In certain embodiments, the dissolution rates of the crystalline molecular complex is higher than the dissolution rate of pinoxaden itself.

The crystalline forms described herein may be characterised using a number of methods known to the skilled person in the art, including single crystal X-ray diffraction, X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), infrared spectroscopy, Raman spectroscopy, nuclear magnetic resonance (NMR) spectroscopy (including solution and solid- state NMR). The purity of the crystalline forms provided herein may be determined by standard analytical methods, such as thin layer chromatography (TLC), gas chromatography, high performance liquid chromatography (HPLC), and mass spectrometry (MS).

In one aspect, the present invention provides a crystalline molecular complex comprising pinoxaden and a carboxylic acid.

A soil pollutant is a persistent toxic material which causes deterioration or loss of one or more soil functions above a certain level. The carboxylic acid in the molecular complex of the present invention does not become a soil pollutant, or does not degrade into a soil pollutant, after the administration of a herbicidally effective amount of the molecular complex to undesired vegetation growing in soil, compost, or other plant-growing medium.

The molar ratio of the pinoxaden : carboxylic acid may be from about 0.1 : about 5 to about 5 : about 0.1. In one embodiment, the molar ratio of the pinoxaden : carboxylic acid may be about 1 : about 1.

The carboxylic acid may be selected from the group consisting of:

(a) the compound of formula (2): wherein: b is an integer which is 0, 1 , 2, 3, 4, or 5; c is an integer which is 0, 1 , 2, 3, 4, or 5; d is an integer which is 0, 1 , 2, 3, 4, or 5;

R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , R ₂₅ , and R ₂₆ are independently selected from the group consisting of -H, -OH, -NH ₂ and - COOH; or the pair of R ₂₁ / R ₂₂ , R ₂₃ / R ₂₄ and/or R ₂₅ / R ₂₆ independently is a carbonyl group.

(b) the compound of formula (3): wherein: e is an integer selected from 0, 1 , 2, 3, 4, 5, 6, 7, or 8; f is an integer selected from 0, 1 , 2, 3, 4, 5, 6, 7, or 8; the symbol denotes that the stereochemistry of the C=C double bond is cis- or trans-;

R ₃₀ is selected from the group consisting of -H, -CO ₂ H, unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl.

(c) the compound of formula (4): wherein: g is an integer selected from 0, 1 , 2, 3, 4 or 5; h is an integer selected from 0, 1 , 2, 3, or 4; W is a carbon atom or a nitrogen atom; Z is absent or is a -CO-NH- group;

R ₄₀ is selected from the group consisting of -OH, -NH ₂ , and -NH-CO- R ₄₃ ;

R ₄₁ and R ₄₂ are independently selected from the group consisting of -H, -OH, unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl;

R ₄₃ is selected from the group consisting of unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ - C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl; provided that when W is a nitrogen atom, g is an integer selected from 0, 1 , 2, 3, or 4.

(d) the compound of formula (5): wherein:

R ₅₀ is selected from the group consisting of -H, unsubstituted C ₁ -C ₂₀ -alkyl, and substituted C ₁ -C ₂₀ -alkyl.

(e) the compound of formula (6): wherein: j is an integer selected from 0, 1 , 2 or 3; k is an integer selected from 0, 1 , 2, 3, or 4;

R ₆₀ and R ₆₁ are independently selected from the group consisting of -H, unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, substituted C ₅ -C ₂₀ -aryl, unsubstituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ -aryl), and substituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ - aryl).

(f) the compound of formula (7): wherein:

R ₇₀ , R ₇₁ , R ₇₂ , R ₇₃ , R ₇₄ , R ₇₅ , R ₇₆ , R ₇₇ , R ₇₈ and R ₇₉ are independently selected from the group consisting of -H, -OH and -COOH, provided that at least one of R ₇₀ , R ₇₁ , R ₇₂ , R ₇₃ , R ₇₄ , R ₇₅ , R ₇₆ , R ₇₇ , R ₇₈ and R ₇₉ is -COOH.

(g) the compound of formula (8): wherein: m is an integer selected from 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10;

R ₈₀ , R ₈₁ , R ₈₂ and R ₈₃ are independently selected from -H, -OH, -COOH and R ₈₄ ; R ₈₄ is the group: wherein:

R ₈₀₀ , R ₈₀₁ , R ₈₀₂ , R ₈₀₃ , R ₈₀₄ , R ₈₀₅ , R ₈₀₆ and R ₈₀₇ are independently selected from the group consisting of -H, -OH, and -COOH; provided that at least one of R ₈₀ , R ₈₁ , R ₈₂ , R ₈₃ , R ₈₀₀ , R ₈₀₁ , R ₈₀₂ , R ₈₀₃ , R ₈₀₄ , R ₈₀₅ , R ₈₀₆ and

R ₈₀₇ is -COOH.

(h) the compound of formula (9): wherein: is a single or double bond; R ₉₀ , R ₉₁ , R ₉₂ , R ₉₃ , R ₉₄ , R ₉₅ , R ₉₆ , and R ₉₇ are independently selected from the group consisting of -H, unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, and -COOH; or the pair of R ₉₀ / R ₉₁ , R ₉₂ / R ₉₃ , R ₉₄ / R ₉₅ and/or R ₉₆ / R ₉₇ independently is a carbonyl group; provided that: (i) when is a double bond, R ₉₅ and R ₉₇ are absent;

(ii) when the pair of R ₉₄ /R ₉₅ and/or R ₉₆ /R ₉₇ is a carbonyl group, is a single bond;

(iii) at least one of R ₉₀ , R ₉₁ , R ₉₂ , R ₉₃ , R ₉₄ , R ₉₅ , R ₉₆ , and R ₉₇ is -COOH.

(g) the compound of formula (10): wherein: is a single or double bond;

R ₁₀₀ , R ₁₀₁ , R ₁₀₂ , R ₁₀₃ , R ₁₀₄ , R ₁₀₅ , R ₁₀₆ , R ₁₀₇ , R ₁₀₈ , R ₁₀₉ and R ₁₁₀ are independently selected from the groups consisting of -H, -OH, unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, and -COOH; or the pair of R ₁₀₀ / R ₁₀₁ , R ₁₀₂ / R ₁₀₃ , R ₁₀₄ /R ₁₀₅ or R ₁₀₆ / R ₁₀₇ independently is a carbonyl group; provided that:

(i) when is a double bond, R ₁₀₂ and R ₁₀₅ are absent; and (ii) when the pair of R ₁₀₄ /R ₁₀₅ and/or R ₁₀₆ /R ₁₀₇ is a carbonyl group, is a single bond.

Compound of formula (2):

When b is selected from 2, 3, 4, or 5, each R ₂₁ may be the same or different to every other R ₂₁ , and each R ₂₂ may be the same or different from every other R ₂₂ . When c is selected from 2, 3, 4, or 5, each R ₂₃ may be the same or different to every other R ₂₃ , and each R ₂₄ may be the same or different from every other R ₂₄ . When d is selected from 2, 3, 4, or 5, each R ₂₅ may be the same or different to every other R ₂₅ , and each R ₂₆ may be the same or different from every other R ₂₆ .

When one of R ₂₁ is different from R ₂₂ , and/or R ₂₃ is different from R ₂₄ , and/or R ₂₅ is different from R ₂₆ , the compound (2) will have one or more chiral carbon atoms. Racemates, enantiomers and diastereomers are within the scope of the invention.

In one embodiment, the compound of formula (2) may be a compound of formula (2a): wherein: b is an integer which is 0, 1 , 2, 3, 4, or 5.

When b is 0, the compound of formula (2a) is oxalic acid i.e. the -COOH groups are bonded directly to each other. When b is 1 , the compound of formula (2a) is malonic acid. When b is 2, the compound of formula (2a) is succinic acid. When b is 3, the compound of formula (2a) is glutaric acid. When b is 4, the compound of formula (3a) is adipic acid. When b is 5, the compound of formula (2a) is pimelic acid.

In another embodiment, the compound of formula (2) may be a compound of formula (2b): wherein:

* denotes a chiral carbon atom, which may have the same or different stereochemistry to any other chiral carbon atom present in the compound; b is an integer which is 0, 1 , 2, 3, 4, or 5; c is an integer which is 0, 1 , 2, 3, 4, or 5; d is an integer which is 0, 1 , 2, 3, 4, or 5;

R ₂₁ , R ₂₃ , and R ₂₅ are independently selected from the group consisting of -OH, -NH ₂ and -COOH.

When b and/or d are not 0 (i.e. are independently selected from 1 , 2, 3, 4, or 5), R ₂₂ , R ₂₄ and R ₂₆ are all -H (and, as such, the hydrogen atoms are not specifically shown in formula (2b)).

Examples of compound of formula (2b) include but are not limited to DL-aspartic acid, L-aspartic acid, D-aspartic acid, DL-glutamic acid, L-glutamic acid, D-glutamic acid, DL-tartaric acid, D-(-)-tartaric acid, L-(+)-tartaric acid, galactaric acid (also known as mucic acid), DL-malic acid, D-malic acid, or L-malic acid.

In another embodiment, the compound of formula (2) may be a compound of formula (2c): wherein: b is an integer which is 0, 1 , 2, 3, 4, or 5; c is an integer which is 0, 1 , 2, 3, 4, or 5; d is an integer which is 0, 1 , 2, 3, 4, or 5; R ₂₃ and R ₂₄ are independently selected from the group consisting of -H, -OH, -NH ₂ and -COOH; provided that when one of R ₂₃ and R ₂₄ is -H, the other of R ₂₃ and R ₂₄ is selected from the group consisting of -OH, -NH ₂ and -COOH; or the pair of R ₂₃ /R ₂₄ is a carbonyl group.

When b and/or d are not 0 (i.e. are independently selected from 1 , 2, 3, 4, or 5), R ₂₁ , R ₂₂ , R ₂₅ and R ₂₆ are -H (and, as such, the hydrogen atoms are not specifically shown in formula (2c)).

Examples of compound of formula (2c) include but are not limited to ketoglutaric acid, or citric acid.

Compound of formula (3):

In one embodiment, R ₃₀ is selected from the group consisting of -H, -CO ₂ H, unsubstituted C ₁ -C ₂₀ - alkyl, and unsubstituted C ₅ -C ₂₀ -aryl. In another embodiment, R ₃₀ is selected from the group consisting of -H, -CO ₂ H and -Me.

In one embodiment, the compound of formula (3) has a cis- stereochemistry i.e. In this instance, R ₃₀ may be selected from the group consisting of -COOH, unsubstituted C ₁ -C ₂₀ -alkyl, and unsubstituted C ₅ -C ₂₀ -aryl, for example, -COOH, -Me or -Ph.

Examples of compound of formula (3a) include but are not limited to maleic acid, oleic acid, or cis- cinnamic acid.

In one embodiment, the compound of formula (3) has a trans- stereochemistry i.e.

In this instance, R ₃₀ may be selected from the group consisting of -COOH, unsubstituted C ₁ -C ₂₀ -alkyl, and unsubstituted C ₅ -C ₂₀ -aryl, for example, -COOH, -Me or -Ph.

Examples of compound of formula (3b) include but are not limited to fumaric acid, or trans-cinnamic acid.

In one embodiment, e is 0 and R ₃₀ is -H. In one instance, the compound (3) may be undecylenic acid. Compound of formula (4):

In one embodiment, the compound of formula (4) may be a compound of formula (4a): wherein: g is an integer selected from 0, 1 , 2, 3, 4 or 5; h is an integer selected from 0, 1 , 2, 3, or 4;

R ₄₀ is selected from the group consisting of -OH, -NH ₂ , and -NH-CO-R ₄₃ ; R ₄₁ and R ₄₂ are independently selected from the group consisting of -H, -OH, unsubstituted C ₁ -C ₂₀ - alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl; and

R ₄₃ is selected from the group consisting of unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl.

In this instance, W is a carbon atom i.e. the 6-membered ring containing W is an aryl group.

In one embodiment, Z is absent (i.e. the group is bonded directly to the aryl ring). In another embodiment, Z is a -CO-NH- group.

In one embodiment, R ₄₀ may be selected from the group consisting of -OH, -NH ₂ and -NH-CO-Me.

R ₄₀ may be present or absent. When absent, g is 0 i.e. the aromatic ring is unsubstituted by R ₄₀ groups. When R ₄₀ is present, g may be 1 , 2, 3, 4, or 5. In one embodiment, the g is an integer selected from 0, 1 , or 2.

When h is 0, the -COOH group may be bonded to -Z- or, if Z is absent, directly to the aromatic ring. In one embodiment, h is selected from 0 or 1 . In one embodiment, h is 0 and g is selected from 0, 1 or 2. In one embodiment, h is 1 and g is selected from 0, 1 , or 2.

When h is selected from 2, 3, or 4, each R ₄₁ may be the same or different to every other R ₄₁ , and each R ₄₂ may be the same or different from every other R ₄₂ . When one of R ₄₁ is different from R ₄₂ , the compound (4a) will have one or more chiral carbon atoms. Racemates, enantiomers and diastereomers are within the scope of the invention.

In one embodiment, R ₄₁ and R ₄₂ are independently selected from the group consisting of -H, and -OH. In another embodiment, one of R ₄₁ and R ₄₂ is -H and the other of R ₄₁ and R ₄₂ is -OH.

In one embodiment, R ₄₁ and R ₄₂ are both -H.

Examples of compound of formula (4a) include but are not limited to benzoic acid, dihydroxybenzoic acid (e.g. 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-dihydroxybenzoic acid), hydroxybenzoic acid (e.g. 2-, 3- or 4- hydroxybenzoic acid), amino-hydroxybenzoic acid (e.g. 4-amino-2-hydroxybenzoic acid), mandelic acid (e.g. D-, L- or DL-mandelic acid), acetamidobenzoic acid (e.g. 2-, 3- or 4-acetamidobenzoic acid), and hippuric acid.

In one embodiment, the compound of formula (4) may be a compound of formula (4b): wherein: g is an integer selected from 0, 1 , 2, 3, or 4; h is an integer selected from 0, 1 , 2, 3, or 4;

Z is absent or is a -CO-NH- group;

R ₄₀ is selected from the group consisting of -OH, -NH ₂ , and -NH-CO-R ₄₃ ;

R ₄₁ and R ₄₂ are independently selected from the group consisting of -H, -OH, unsubstituted C ₁ -C ₂₀ - alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl; and R ₄₃ is selected from the group consisting of unsubstituted C ₁ -C ₂₀ -alkyl, substituted C ₁ -C ₂₀ -alkyl, unsubstituted C ₅ -C ₂₀ -aryl, and substituted C ₅ -C ₂₀ -aryl.

In this instance, W is a nitrogen atom i.e. the 6-membered ring containing W is a pyridinyl ring g, h, Z R ₄₀ , R ₄₁ , R ₄₂ and R ₄₃ are as described above for the compound of formula (4a).

In one embodiment, the compound of formula (4b) may be nicotinic acid.

Compound of formula (5):

In one embodiment, R ₅₀ is selected from the group consisting of -H, unsubstituted C ₁ -C ₂₀ -alkyl, and substituted C ₁ -C ₂₀ -alkyl, and the substituents are selected from the group consisting of -OH and -NH ₂ .

Examples of compound of formula (5) include but are not limited to formic acid, glycolic acid, acetic acid, caproic acid, propionic acid, stearic acid or caprylic acid.

Compound of formula (6):

R ₆₀ may be present or absent. When absent, j is 0 i.e. the aromatic ring is unsubstituted. When R ₆₀ is present, j may be 1 , 2, or 3. In one embodiment, the j is an integer selected from 0 or 1 .

R ₆₀ may be selected from the group consisting of -OH and substituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ -aryl), wherein the substituents are selected from the group consisting of -OH and -COOH. An example of a substituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ -aryl) group includes but is not limited to -CH ₂ -(3-hydroxy-2- naphthoic acid).

R ₆₁ may be present or absent. When absent, k is 0 i.e. the aromatic ring is unsubstituted. When R ₆₁ is present, k may be 1 , 2, 3, or 4. R ₆₁ may be selected from the group consisting of -OH and substituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ -aryl), wherein the substituents are selected from the group consisting of -OH and -COOH. An example of a substituted -(C ₁ -C ₂₀ -alkyl)-(C ₅ -C ₂₀ -aryl) group includes but is not limited to -CH ₂ -(3-hydroxy-2- naphthoic acid).

In one embodiment, the compound of formula (6) may be a compound (6a):

R ₆₀ and j are as described above. In this instance, R ₆₁ is absent i.e. k is 0.

Examples of compounds (6) include but are not limited to hydroxy-naphthoic acid (e.g. 1-hydroxy-2- napthoic acid) and pamoic acid.

Compound of formula (7):

One of R ₇₀ and R ₇₁ may be -H and the other of R ₇₀ and R ₇₁ may be -OH. One of R ₇₂ and R ₇₃ may be - H and the other of R ₇₂ and R ₇₃ may be -OH. One of R ₇₄ and R ₇₅ may be -H and the other of R ₇₄ and R ₇₅ may be -OH. One of R ₇₆ and R ₇₇ may be -H and the other of R ₇₆ and R ₇₇ may be -OH. One of R ₇₈ and R ₇₉ may be -H and the other of R ₇₈ and R ₇₉ may be -COOH.

An example of compound of formula (7) includes but is not limited to D-glucuronic acid.

Compound of formula (8):

When m is 2, 3, 4, 5, 6, 7, 8, 9, or 10, each R ₈₁ may be the same or different to every other R ₈₁ , and each R ₈₂ may be the same or different from every other R ₈₂ . When one of R ₈₁ is different from R ₈₂ , the compound (8) will have one or more chiral carbon atoms. Racemates, enantiomers and diastereomers are within the scope of the invention.

Compound (8) may be substituted with one or more R ₈₄ groups up to the limitations imposed by stability, for example, one R ₈₄ group or more than one (e.g. two R ₈₄ groups).

The glycosidic bond at the animeric carbon atom of R ₈₄ group may be in the a- or b- position.

One of R ₈₀₀ and R ₈₀₁ may be -H and the other of R ₈₀₀ and R ₈₀₁ may be -OH. One of R ₈₀₂ and R ₈₀₃ may be -H and the other of R ₈₀₂ and R ₈₀₃ may be -OH. One of R ₈₀₄ and R ₈₀₅ may be -H and the other of R ₈₀₄ and R ₈₀₅ may be -OH. R ₈₀₆ and R ₈₀₇ may be selected from -H or -OH. In one embodiment, R ₈₀₆ is -H and R ₈₀₇ is -OH.

Examples of compound of formula (8) include but are not limited to lactic acid (e.g. DL-, D- or L-lactic acid), glucoheptonic acid (e.g. D-glucoheptonic acid), lactobionic acid, and gluconic acid (e.g. DL-, D- or L-gluconic acid).

Compound of formula (9):

In one embodiment, R ₉₀ , R ₉₁ , R ₉₂ , R ₉₃ , R ₉₄ , R ₉₅ , R ₉₆ , and R ₉₇ are independently selected from the group consisting of -H, unsubstituted C ₁ -C ₂₀ -alkyl, and -COOH; or the pair of R ₉₀ /R ₉₁ , R ₉₂ /R ₉₃ , R ₉₄ /R ₉₅ or R ₉₆ /R ₉₇ independently is a carbonyl group.

In one embodiment, is a double bond and R ₉₄ and R ₉₅ are independently selected from -H and - COOH.

In one embodiment, the pairs R ₉₀ /R ₉₁ and R ₉₂ /R ₉₃ are both carbonyl groups.

An example of a compound of formula (9) includes but is not limited to orotic acid. Compound of formula (10):

In one embodiment, is a single bond. In another embodiment, is a double bond.

In one embodiment, V is a group i.e. compound (10) is a five-membered carbocyclic ring. In another embodiment, V is a -O- group. In another embodiment, V is

R ₁₀₀ , R ₁₀₁ , R ₁₀₂ , R ₁₀₃ , R ₁₀₄ , R ₁₀₅ , R ₁₀₆ , and R ₁₀₇ may be independently selected from the group consisting of -H, -OH and substituted C ₁ -C ₂₀ -alkyl, wherein the substituent is one or more -OH groups.

In one embodiment, the pair of R ₁₀₀ /R ₁₀₁ , or R ₁₀₆ /R ₁₀₇ independently is a carbonyl ) group.

In one embodiment, at least of R ₁₀₀ , R ₁₀₁ , R ₁₀₂ , R ₁₀₃ , R ₁₀₄ , R ₁₀₅ , R ₁₀₆ , and R ₁₀₇ is a -COOH group.

Compound (10) have one or more chiral carbon atoms. Racemates, enantiomers and diastereomers are within the scope of the invention. Examples of compounds of formula (10) include but are not limited to pyroglutamic acid (e.g. DL-, D- or L-pyroglutamic acid), camphoric acid (e.g. (+)- or (-)-camphoric acid), and ascorbic acid (e.g. DL-, D-, or L-ascorbic acid).

In one embodiment, the carboxylic acid may be selected from the group consisting of benzoic acid, salicylic acid, aminobenzoic acid (e.g. 4-aminobenzoic acid), and dihydroxybenzoic acid (e.g. 2,5- dihydroxybenzoic acid).

In one embodiment, the carboxylic acid is not benzoic acid.

In one embodiment, the molecular complex is a crystalline pinoxaden benzoic acid molecular complex. The molecular complex may have an X-ray powder diffraction pattern comprising one or more peaks (for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10 peaks) selected from the group consisting of about 7.7, 9.3,

10.4, 11.1 , 11.4, 11.9, 12.9, 14.3, 15.3, 16.3, 16.6, 17.0, 17.6, 18.0, 18.6, 19.2, 19.5, 20.6, 20.9, 21.2, 21 .9, 22.3, 23.0, 23.3, 23.9, 24.9, 25.3, 25.8, 26.1 , 28.4, 31 .8, 32.1 , and 32.8 degrees two-theta ± 0.2 degrees two-theta. In one embodiment, the molecular complex may have the X-ray powder diffraction pattern substantially as shown in Figure 1 .

The molecular complex may have a DSC thermogram comprising an endothermal event with an onset temperature at about 114.2 °C. In one embodiment, the molecular complex may have a DSC thermogram substantially as shown in Figure 2.

In one embodiment, the molecular complex is a crystalline pinoxaden salicylic acid molecular complex. The molecular complex may have an X-ray powder diffraction pattern comprising one or more peaks (for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10 peaks) selected from the group consisting of about 7.6, 8.3, 9.1 , 9.5, 10.2, 10.9, 11.2, 11.8, 12.8, 14.1 , 14.6, 15.3, 16.2, 16.5, 17.0, 17.5, 18.3, 18.4, 18.8, 19.5,

20.2, 20.6, 20.9, 21.3, 21.8, 22.4, 23.1 , 23.4, 23.6, 24.1 , 24.6, 25.0, 25.3, 25.7, 26.0, 26.3, 27.2, 27.4,

28.2, 28.9, 29.5, 29.8, 31 .3, 31.9, 32.6, 33.2, 33.5, 34.8, 35.3, and 38.9 degrees two-theta ± 0.2 degrees two-theta. In one embodiment, the molecular complex may have the X-ray powder diffraction pattern substantially as shown in Figure 3.

The molecular complex may have a DSC thermogram comprising an endothermal event with an onset temperature at about 137.6 °C. In one embodiment, the molecular complex may have a DSC thermogram substantially as shown in Figure 4.

In one embodiment, the molecular complex is a crystalline pinoxaden 4-aminobenzoic acid molecular complex. The molecular complex may have an X-ray powder diffraction pattern comprising one or more peaks (for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10 peaks) selected from the group consisting of about

7.1. 8.4, 8.7, 11.1 , 12.2, 13.4, 14.2, 15.4, 15.6, 16.0, 16.6, 17.1 , 17.3, 17.8, 18.5, 18.9, 19.1 , 19.4, 19.7, 21 .0, 21 .5, 21 .8, 22.4, 23.0, 23.2, 23.6, 23.8, 24.2, 24.5, 25.1 , 25.4, 25.8, 26.1 , 26.4, 26.8, 27.2, 27.4, 27.6, 27.8, 28.5, 28.9, 29.5, 30.1 , and 32.5 degrees two-theta ± 0.2 degrees two-theta. In one embodiment, the molecular complex may have the X-ray powder diffraction pattern substantially as shown in Figure 5.

The molecular complex may have a DSC thermogram comprising an endothermal event with an onset temperature at about 132.1 °C. In one embodiment, the molecular complex may have a DSC thermogram substantially as shown in Figure 6.

In one embodiment, the molecular complex is a crystalline pinoxaden 2,5-dihydroxybenzoic acid molecular complex. The molecular complex may have an X-ray powder diffraction pattern comprising one or more peaks (for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10 peaks) selected from the group consisting of about 7.5, 8.2, 8.7, 9.7, 10.1 , 10.4, 10.9, 11.6, 11.8, 12.4, 13.6, 15.2, 15.9, 16.5, 16.7, 17.3, 17.6, 18.1 , 18.6, 19.0, 19.3, 19.8, 20.3, 21.1 , 21.3, 22.0, 22.4, 22.8, 23.6, 25.3, 25.7, 26.7, 27.5, 28.6, and 30.0 degrees two-theta ± 0.2 degrees two-theta. In one embodiment, the molecular complex may have the X-ray powder diffraction pattern substantially as shown in Figure 7.

The molecular complex may have a DSC thermogram comprising an endothermal event with an onset temperature at about 134.6 °C. In one embodiment, the molecular complex may have a DSC thermogram substantially as shown in Figure 8.

The crystalline pinoxaden carboxylic acid molecular complexes may be prepared by a process comprising the steps of:

(a) forming a solution of pinoxaden and a carboxylic acid in a solvent selected from tetrahydrofuran (THF), isopropyl alcohol (IPA), or a mixture thereof;

(b) forming a solution or suspension of molecular complex in the solvent; and

(c) recovering the molecular complex as a crystalline solid.

Pinoxaden and the carboxylic acids are as described above.

In one embodiment, the solvent is THF. In another embodiment, the solvent is IPA. In yet another embodiment, the solvent is a mixture of THF and IPA.

The quantity of solvent is not particularly limiting provided there is enough solvent to substantially dissolve pinoxaden and the carboxylic acid. If a suspension or hazy solution remains on contacting pinoxaden and/or the carboxylic acid with the solvent, a second or further quantities of solvent may be added until a solution is formed or the suspension or hazy solution may be filtered.

The solution of pinoxaden and the carboxylic acid may formed at ambient temperature or less. Alternatively, the pinoxaden and the carboxylic acid may be contacted with the solvent at a temperature greater than ambient i.e. greater than 30 °C and below the boiling point of the reaction mixture. The boiling point of the reaction mixture may vary depending on the pressure under which the contacting step is conducted. In one embodiment, the contacting step is carried out at atmospheric pressure (i.e. 1.0135 × 10 ⁵ Pa). In one embodiment, the contacting step may be carried out at one or more temperatures in the range of ³ about 40 °C to about £ 60 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 40 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 41 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 42 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 43 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 44 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 45 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 46 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 47 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 48 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 49 °C. In some embodiments, the contacting step is carried out at one or more temperatures ³ about 50 °C.ln some embodiments, the contacting step is carried out at one or more temperatures £ about 60 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 59 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 58 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 57 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 56 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 55 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 54 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 53 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 52 °C. In some embodiments, the contacting step is carried out at one or more temperatures £ about 51 °C. In one embodiment, the contacting step is carried out at one or more temperatures in the range of ³ about 45 °C to £ about 55 °C. In one embodiment, the contacting step is carried out at a temperature of about 50 °C.

The dissolution of pinoxaden and/or the carboxylic acid may be encouraged through the use of an aid such as stirring, shaking and/or sonication.

The solution or suspension may then be cooled such that the resulting solution or suspension has a temperature below that of the solution or suspension step (b). The rate of cooling may be from about 0.05 °C/minute to about 2 °C/minute, such as about 0.5 °C/minute to about 1.5 °C/minute, for example about 1 °C/minute. When a solution of molecular complex is cooled, a suspension may eventually be observed. When a suspension of molecular complex is cooled, no perceptible change in the appearance of the suspension may occur. The solution or suspension may be cooled to ambient temperature or a temperature of less than ambient temperature. In one embodiment, the solution or suspension may be cooled to one or more temperatures in the range of ³ about 0 °C to about £ 20 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures ³ about 1 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures ³ about 2 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures ³ about 3 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures ³ about 4 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures ³ about 5 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures £ about 15 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures £ about 14 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures £ about 13 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures £ about 12 °C. In some embodiments, the solution or suspension may be cooled to one or more temperatures £ about 11 °C. In some embodiments, the solution or suspension is cooled to one or more temperatures £ about 10 °C. In one embodiment, the solution or suspension is cooled to one or more temperatures in the range of about 0 °C to about 10 °C, for example, about 5 °C.

In step (c), the molecular complex is recovered as a crystalline solid. The crystalline molecular complex may be recovered by directly by filtering, decanting or centrifuging. The crystalline molecular complex formed may be optionally slurried in a suitable solvent or solvent mixture (e.g. acetone, heptane, or a mixture thereof) in order to purify the crystalline molecular complex or remove an excess of one of the starting materials.

Howsoever the crystalline molecular complex is recovered, the separated solid may be washed one or more times with a suitable solvent or solvent mixture (e.g acetone, heptane, or a mixture thereof) and dried. Drying may be performed using known methods, for example, at temperatures in the range of about 10 °C to about 60 °C, such as about 20 °C to about 40 °C, for example, ambient temperature under vacuum (for example about 1 mbar to about 30 mbar) for about 1 hour to about 24 hours. It is preferred that the drying conditions are maintained below the point at which the molecular complex degrades and so when the molecular complex is known to degrade within the temperature or pressure ranges given above, the drying conditions should be maintained below the degradation temperature or vacuum.

Steps (a) to (c) may be carried out one or more times (e.g. 1 , 2, 3, 4 or 5 times). When steps (a) to (c) are carried out more than once (e.g. 2, 3, 4 or 5 times), step (a) may be optionally seeded with crystalline molecular complex which was previously prepared and isolated by the first iteration of steps (a) to (c).

Alternatively or in addition, when steps (a) to (c) are carried out more than once (e.g. 2, 3, 4 or 5 times), the solution or suspension formed in step (b) may be optionally seeded with crystalline molecular complex (which was previously prepared and isolated by a method described herein). The molecular complex may be formulated into a herbicidal composition with at least one agriculturally acceptable carrier. The compositions may be solids, for example powders, granules, or water- dispersable powders, or may be liquids, such as suspensions of molecular complex particles.

Suitable agriculturally acceptable carriers are well known to those skilled in the art. Such carriers should not be phytotoxic to crops, in particular at the concentrations employed for the control of undesirable plants in the presence of crops, and should not react chemically with the compounds of the molecular complex or other composition components. The compositions may be applied directly, or may be formulations or concentrates which are diluted, for example with water, prior to application.

Liquid carriers that may be employed include water and organic solvents, although it is typically preferred that water is used. Solid carriers include mineral earths, such as clays, silicates, diatomaceous earths, or kaolin, fertilisers, and organic products such as woodmeal and cellulose carriers.

It will be understood by the skilled person that the compositions may also include further components, such as surfactants, viscosity modifiers, anti-freeze agents, agents for pH control, stabilisers and anti- caking agents.

The concentration of active ingredients in the composition is generally between about 1 and about 99 wt%, such as between about 5 and about 95 wt% or about 10 and about 90 wt%. In compositions which are designed to be diluted prior to use the concentration of active ingredients may be between about 10 and about 90 wt%. Such compositions are then diluted, for example with water, to compositions which may contain about 0.001 and about 1 wt% of active material.

The compositions as described herein may be used for controlling or substantially eliminating undesirable vegetation. Undesirable vegetation is understood to mean plants considered undesirable in a particular location, e.g. in an area of crops, and may be known as weeds.

Control may be achieved by a method comprising contacting the vegetation with the herbicidal composition. It will be understood by the skilled person that the composition at the point of application should contain a herbicidally effective amount of the molecular complex. A herbicidally effective amount is an amount of the active ingredients which causes an adverse deviation of the natural development of the undesired vegetation.

The compositions may have utility for controlling undesirable vegetation in a culture of crop plants, especially crop plants which are tolerant to the pinoxaden herbicide, for example through genetic modification of the crop plants. The compositions may also have utility for the control of undesirable vegetation which is resistant to pinoxaden. Embodiments and/or optional features of the invention have been described above. Any aspect of the invention may be combined with any other aspect of the invention, unless the context demands otherwise. Any of the embodiments or optional features of any aspect may be combined, singly or in combination, with any aspect of the invention, unless the context demands otherwise.

The invention will now be described further by reference to the following examples, which are intended to illustrate but not limit, the scope of the invention.

Examples

Instrument and Methodology Details X-Ray Powder Diffraction (XRPD)

XRPD diffractograms were collected on a Bruker D8 diffractometer. Bruker D8 uses Cu Ka radiation (40 kV, 40 mA) and a q-2q goniometer fitted with a Ge monochromator. The incident beam passes through a 2.0 mm divergence slit followed by a 0.2 mm anti-scatter slit and knife edge. The diffracted beam passes through an 8.0 mm receiving slit with 2.5° Soller slits followed by the Lynxeye Detector. The software used for data collection and analysis was Diffrac Plus XRD Commander and Diffrac Plus EVA respectively.

Samples were run under ambient conditions as flat plate specimens using powder as received. The sample was prepared on a polished, zero-background (510) silicon wafer by gently pressing onto the flat surface or packed into a cut cavity. The sample was rotated in its own plane.

The details of the standard collection method are:

• Angular range: 2 to 42° 2q

• Step size: 0.05° 2q

• Collection time: 0.5 s/step (total collection time: 6.40 min)

DSC method

DSC (melting point) was assessed using either a TA Instruments Q2000 or TA Instruments Discovery DSC. Typically, 0.5 - 3 mg of each sample, in a pin-holed aluminium pan, was heated at 10 °C/min from 25 °C to 300 °C. A purge of dry nitrogen at 50 ml/min was maintained over the sample.

Starting Materials

Pinoxaden was purchased from PTG Advanced Catalyst Co.

The carboxylic acids were purchased from Sigma Aldrich.

Example 1 Pinoxaden: benzoic acid (1:1) molecular complex

Pinoxaden (20 mg) (PTG Advanced Catalyst Co.) and benzoic acid (6 mg) (Sigma-Adrich) were added to a vial and dissolved using THF (200 ml). The clear solution was left to evaporate at RT overnight forming a gum, which became a crystalline solid after several days. The XRPD of the crystalline solid was consistent with that in Figure 1.

Example 2 Pinoxaden: benzoic acid (1:1) molecular complex Pinoxaden (300 mg) (PTG Advanced Catalyst Co) and benzoic acid (91 mg, 1 mol eq.) (Sigma Aldrich) were stirred in IPA (0.98 ml) at 50 °C. The resulting solution was allowed to cool to 40 °C and seeded with the crystalline solid of Example 1. The sample was cooled to 5 °C at 0.1 °C/min. The resulting suspension was filtered and dried, then further slurried in 5% acetone/heptane for 45 minutes, prior to filtration. The solid was analysed by XRPD, which showed a crystalline material and yielded a diffractogram as provided in Figure 1.

The following table provides an XRPD peak list for the Pinoxaden: benzoic acid (1 :1) molecular complex:

The molecular complex was also characterised by DSC (Figure 2). DSC analysis indicated a melting point with an onset temperature of about 114.2 °C. Example 3 Pinoxaden: salicylic acid (1:1) molecular complex

Pinoxaden (300 mg) (PTG Advanced Catalyst Co) and salicylic acid (103 mg, 1 mol eq.) (Sigma Aldrich) were stirred in THF (1 .2 ml) at 50 °C. The sample was cooled to 5 °C a thick suspension was obtained. Antisolvent, heptane (2 ml) was then added. The resulting suspension was filtered and allowed to air-dry at room temperature. XRPD analysis of the solid showed a crystalline material which yielded a diffractogram as provided in Figure 3.

The following table provides an XRPD peak list for the Pinoxaden: salicylic acid (1 :1) molecular complex: The molecular complex was also characterised by DSC (Figure 4). DSC analysis indicated a melting point with an onset temperature of about 137.6 °C.

Example 4 Pinoxaden (20 mg) (PTG Advanced Catalyst Co) and 4-aminobenzoic acid (6.9 mg) (Sigma Aldrich) were added to a vial and dissolved using THF (200 ml). The clear solution was left to evaporate at RT overnight and formed a gum which became a crystalline solid after several days. The XRPD of the crystalline solid was consistent with that in Figure 5. Example 5 Pinoxaden: 4-aminobenzoic acid (1:1) molecular complex

Pinoxaden (300 mg) (PTG Advanced Catalyst Co) and 4-aminobenzoic acid (103 mg, 1 mol eq.) (Sigma Aldrich) were stirred in IPA (1.38 ml) at 50 °C. The resulting solution was allowed to cool to 40 °C and seeded with the crystalline solid of Example 4. The sample was cooled to 5 °C at 0.1 °C/min and held at 5 °C. The resulting suspension was filtered. XRPD analysis of the solid showed a crystalline material which yielded a diffractogram as provided in Figure 5.

The following table provides an XRPD peak list for the Pinoxaden: 4-aminobenzoic acid (1 :1) molecular complex:

The molecular complex was also characterised by DSC (Figure 6). DSC analysis indicated a melting point with an onset temperature of about 132.1 °C. Example 6 Pinoxaden: 2.5-dihvdroxybenzoic acid (1:1)

Pinoxaden (20 mg) (PTG Advanced Catalyst Co) and 2,5-dihydroxybenzoic acid (8 mg) (Sigma Aldrich) were added to a vial and dissolved using THF (200 ml). The clear solution was left to evaporate at RT overnight and formed a crystalline solid residue. The XRPD of the crystalline solid was consistent with that in Figure 7.

Example 7 Pinoxaden: 2.5-dihvdroxybenzoic acid (1 :1) co-crystal

Pinoxaden (300 mg) (PTG Advanced Catalyst Co) and 2,5-dihydroxybenzoic acid (115 mg, 1 mol eq.) (Sigma Aldrich) were stirred in IPA (1.38 ml) at 50 °C. The resulting solution was allowed to cool to 40 °C and seeded with the crystalline solid of Example 7. The sample was cooled to 5 °C at 0.1 °C/min and held at 5 °C. The resulting suspension was filtered. XRPD analysis of the solid showed a crystalline material which yielded a diffractogram as provided in Figure 7.

The following table provides an XRPD peak list for the Pinoxaden: 2,5-dihydroxybenzoic acid (1 :1) molecular complex:

The molecular complex was also characterised by DSC (Figure 8). DSC analysis indicated a melting point with an onset temperature of about 134.6 °C.