Title of Invention	COMPOSITION COMPRISING BRANCHED CARBOXYLIC ACID DIESTERS AND PREPARATION PROCESSES THEREOF
Abstract	Branched carboxylic acid diesters The present invention relates to carboxylic acid diesters exhibiting in particular advantageous solvating properties which can be used as a substitute for conventional solvents, in particular halogenated solvents. The invention relates more particularly to a composition formed of branched carboxylic acid diesters which are obtained from a mixture of branched dinitriles and to its use as solvent in numerous industrial applications.

Title of Invention

COMPOSITION COMPRISING BRANCHED CARBOXYLIC ACID DIESTERS AND PREPARATION PROCESSES THEREOF

Abstract

Full Text	Branched carboxylic acid diesters The present invention relates to carboxylic acid diesters exhibiting in particular advantageous solvating properties which can be used as a substitute for conventional solvents, in particular halogenated solvents. The invention relates more particularly to a composition formed of branched carboxylic acid diesters which are obtained from a mixture of dinitriles. This mixture of dinitriles is obtained as distillation fraction during the recovery and purification of adiponitrile in the process for the manufacture of the latter compound by double hydrocyanation of butadiene. An oxygenated solvent has been provided for several years. This solvent is based on diesters obtained by esterification of a mixture of dicarboxylic acids, more particularly of a mixture of adipic acid, glutaric acid and succinic acid. This mixture of acids is obtained in the process for the manufacture of adipic acid by oxidation of cyclohexanol and/or cyclohexanone. This solvent, for example sold by Rhodia under the trade name Rhodiasolv RPDE or by Invista under the trade name DBE, is used in numerous applications, in particular as a replacement for hydrocarbon solvents, chlorinated solvents or oxygenated solvents (glycol ethers, acetone). In addition to this technical performance, which is a result of its solvating power and of its physicochemical properties, this oxygenated solvent exhibits the advantage of being less damaging to the envirormient, of being biodegradable and of being easy to recycle. Its highly favourable toxicological profile makes it possible to eliminate any risk to the final user. In addition, the physicochemical properties, such as the low volatility and the flash point, allow it to be used in complete safety. It can also be used as a mixture with other solvents, such as N-methylpyrrolidone (NMP), without affecting the solvent properties but while reducing the cost of this. Furthermore, this solvent is stable at ambient temperature and exhibits a low vapour pressure. Oxygenated solvents exhibiting good solvating properties and without risk of toxicity and without danger to the environment are experiencing very strong growth. It is therefore important for the industrial sector to find and provide novel solvents exhibiting properties at least similar or equivalent to those of the solvents already available, such as the abovementioned RPDE. One of the aims of the present invention is to provide a novel oxygenated solvent exhibiting physical properties, solvent properties, a toxicological profile and an ecotoxic impact which are similar or improved with respect to the solvent based on diesters of a mixture of adipic acid, glutaric acid and succinic acid. To this end, the invention provides a novel composition comprising a mixture of diesters of ethylsuccinic acid, methylglutaric acid and optionally adipic acid. According to another characteristic of the invention, this mixture comprises: > from 70 to 95% by weight of methylglutaric acid diesters > from 5 to 30% by weight of ethylsuccinic acid diesters > from 0 to 10% by weight of adipic acid diesters This composition is obtained starting from a mixture of dinitrile compounds in particular produced and recovered in the process for the manufacture of adipo-nitrile by double hydrocyanation of butadiene. This process, used on a large scale industrially to produce the great majority of adiponitrile consumed in the world, is described in numerous patents and works. The reaction for the hydrocyanation of butadiene results predominantly in the formation of linear dinitriles but also in the formation of branched dinitriles, the two main ones of which are methylglutaronitrile and ethylsuccinonitrile. In the stages of separation and purification of the adiponitrile, the branched dinitrile compounds are separated by distillation and recovered, for example as top fraction in a distillation column. The invention provides for the conversion of this mixture of branched dinitrile compounds mto diesters in order thus to produce a novel solvent. It can be of interest to eliminate more volatile compounds from the recovered branched dinitrile compounds by a simple distillation for example. One of the possible processes for the conversion of dinitrile compounds to diesters corresponds to the use of the Pinner reaction, described in particular in French Patent No. 1 488 857. Basically, this process consists in reacting the dinitrile compounds with an alcohol in the presence of a strong inorganic acid, such as sulphvuric acid, and in then hydrolysing the products obtained in order to recover the diesters by distillation. This document also describes a specific embodiment of the process which consists in passing the mixture of dinitrile compounds and the alcohol into a bath of molten salts based on various alkali metal and ammonium sulphates in order to prevent the formation of ammonium sulphate and to recover aqueous ammonia by extraction with steam. The diesters of the invention can also be obtained by a reaction between the dinitrile compounds, water and an alcohol in the gas phase and in the presence of a solid catalyst. The reaction temperature is advantageously greater than the condensation temperature of the diesters formed. Use may be made, as catalyst, of a solid acid catalyst, such as, for example, a silica gel, a silica/alumina mixture, zeolites, zirconia or supported boric or phosphoric acids. Use may also be made of macroporous aluminas, such as those described in European Patent EP 0 805 801. The temperature of the reaction is between 200 and 450°C, preferably between 230 and 350°C. The reaction can be carried out under any pressure, advantageously of between 0.1 and 20 bar. At the reactor outlet, the vapours are rapidly cooled to a temperature of less than or equal to 150°C. The ammonia, then the water and the alcohol in excess are separated by distillation from the mixture obtained. The diesters of the invention can also be obtained by reaction between the dinitrile compounds and an inorganic base, in order to obtain acid salts, then neutralization of these salts by an acid, followed by esterification with an alcohol. Salts of diacids and in particular the ammonium salt of the diacids can be obtained by enzymatic hydrolysis of the nitrile compounds, such as described, for example, in Patents EP596812,FR2700777. Finally, the diesters are purified according to purification processes conventionally used in the technical field of the preparation of organic compounds and in particular by distillation in one or more columns. According to the invention, the mixture of diesters in accordance with the invention exhibits specific properties different from the properties of the mixture of diesters obtained by esterification of linear carboxylic acids. More particularly, it exhibits a crystallization temperature of less than -50°C, which makes possible use within a very broad temperature range with a low viscosity of the solvent. By way of comparison, the solvent resulting from the mixture of linear carboxylic acids has a crystallization temperature of between -20°C and +20°C, depending on their composition. The composition of the invention also exhibits a low solubility in water. Equally, the solubility of water in the composition is less than 2.5% by weight at 23°C. The diesters forming the composition according to the invention are obtained by reaction of an alcohol with the abovementioned dinitrile compounds. Mention may be made, as alcohol which can be used for the manufacture of these compounds, of branched or unbranched and cyclic or acyclic aliphatic alcohols which can comprise an aromatic ring and which can comprise from 1 to 20 carbon atoms. Mention may be made, as preferred examples, of the following alcohols: methanol, propanol, isopropanol, benzyl alcohol, ethanol, n-butanol, isobutanol, pentanols, cyclohexanol, hexanol, isooctanol or 2-ethylhexanol. f The composition of the invention can be used alone or as a mixture with other solvents or with water in the form of a solution or emulsion. In particular, they can be used as a mixture with the diesters of the linear diacids mentioned above. These compositions have applications as solvent in numerous fields, such as paints, varnishes and lacquers, the industry for coating surfaces or any other article, such as cables, for example, the ink industry, lubricants for textiles, binders and resins for foundry cores and moulds, cleaning products, cosmetic formulations, for the implementation of certain chemical reactions, in soil and plant treatment compositions and more generally the use, alone or in a formulation, as cleaning, pickling or degreasing solvent in any industrial or domestic activity. These compositions can also be used as plasticizers for some plastics or as monomers for the manufacture of polymers. Other advantages or characteristics of the invention will be described in more detail and will be better illustrated in the light of the examples given below purely by way of illustration. Example 43.26 g of a mixture A of dinitrile compounds are charged with 76.90 g of methanol to a glass reactor with a capacity of 500 ml equipped with a vertical reflux condenser and a stirrer and heated by an oil bath. The mixture A of dinitrile compounds is composed of: > 8 6.9% by weight of methylglutaronitrile > 11.2% by weight of ethylsuccinonitrile > 1.9% by weight of adiponitrile. The remainder to 100% corresponds to the impurities present in this mixture, which are generally not dinitrile compounds. The dinitrile compounds/methanol mixture is cooled to approximately 1 °C before the addition of 84.22 g of 98% by weight sulphuric acid. The reaction medium is heated to reflux and is maintained at this temperature for 3 h. The reaction mass is heterogeneous and fluid. After cooling to 60°C, 63 g of water are added. The reaction medium is maintained at 65°C for 2 hours. 117 g of additional water are then added. The reaction medium becomes two-phase. After removing the excess methanol by evaporation, the two phases are separated by settling and analysed. The organic phase recovered is washed with a saturated aqueous sodium chloride solution with addition of aqueous ammonia in order to obtain a pH in the region of 7. Washing is carried out a second time with a saturated aqueous sodium chloride solution. This mixture exhibits the following properties: > Crystallization temperature (the crystallization point was determined by use of the method described in Standard NFT 20-051): less than -50°C > Solubility with water: 0 Solubility of water in the composition: 2.2% by weight o Solubility of the composition in water: 2.5% by weight This value was determined using a container equipped with a stirrer at a temperature of 23 °C, either by addition of water to 20 g of diester composition or by addition of the diester composition to 50 g of water, until a cloudy solution was obtained. Resistance to hvdrolvsis: Acidity is produced by adding 5 g of diester composition to 95 g of water comprising 8 millimol of NaOH. The flask is placed for several days in a chamber heated to 50°C. The acidity of the medium is measured periodically in order to monitor the fall in the pH. These tests were carried out with the diester composition of the invention and, by way of comparison, with a diester composition resulting from a mixture of linear diacids sold by Rhodia under the trade name RPDE. They show that the composition of the invention is more resistant to hydrolysis than the RPDE composition. Likewise, comparative tests were carried out in order to evaluate the solvating power of the diesters of the invention in comparison with that of the RPDE composition of Rhodia. These tests were carried out by mixing, in a container, resins commonly employed in the painting field with a predetermined amount of solvent formed of diesters or RPDE. The results observed are listed in Tables I and II below: The above tests show that the solvating power of the diesters of the invention is at least equivalent to that of the solvent RPDE. CLAIMS 1. Composition comprising a mixture of diesters of ethylsuccinic acid and of methylglutaric acid. 2. Composition according to Claim 1, characterized in that it comprises diesters of adipic acid. 3. Composition according to either of Claims 1 and 2, characterized in that the concentration by weight of its various components is: > diesters ofmethylglutaric acid ofbetween 70 and 95% > diesters of ethylsuccinic acid of between 5 and 30% > diesters of adipic acid of between 0 and 10% 4. Composition according to one of the preceding claims, characterized in that it exhibits a crystallization temperature of less than -50°C. 5. Composition according to one of the preceding claims, characterized in that the solubility of water in the said composition is less than or equal to 2.5% by weight at 23°C. 6. Composition according to one of the preceding claims, characterized in that it is obtained by esterification of corresponding dinitrile compounds. 7. Composition according to Claim 6, characterized in that the dinitrile compounds used are present in the mixture of the branched dinitriles which are separated from adiponitrile in the process for the manufacture of adiponitrile by double hydrocyanation of butadiene. 8. Composition according to one of the preceding claims, characterized in that the diesters are obtained by reaction of a dinitrile compound with an alcohol chosen from the group consisting of branched or unbranched and cyclic or acyclic aliphatic alcohols which can comprise an aromatic ring and which can comprise from 1 to 20 carbon atoms. 9. Composition according to Claim 8, characterized in that the alcohol is chosen from the group consisting of methanol, propanol, isopropanol, benzyl alcohol, ethanol, n-butanol, isobutanol, pentanols, cyclohexanol, hexanol, isooctanol and 2-ethylhexanol. 10. Process for the manufacture of a diester composition according to one of the preceding claims, characterized in that it consists in reacting a dinitrile compound with an alcohol in the presence of a strong inorganic acid, in then hydrolysing the medium and in recovering the diester composition. 11. Process for the manufacture of a diester composition according to one of Claims 1 to 9, characterized in that it consists in reacting the dinitriles with water and an alcohol in the gas phase in the presence of a solid catalyst. 12. Process according to Claim 11, characterized in that the catalyst is a solid acid catalyst. 13. Process according to Claim 11, characterized in that the catalyst is a macroporous alumina. 14. Process for the manufacture of a diester composition according to one of Claims 1 to 9, characterized in that it consists in reacting the dinitriles with a basic compound, in order to obtain acid salts, in neutralizing these salts with an acid and in then esterifying the acids obtained by reaction with an alcohol. 15. Use of a composition according to one of Claims 1 to 9 as solvent or cosolvent.

Full Text

Branched carboxylic acid diesters
The present invention relates to carboxylic acid diesters exhibiting in particular advantageous solvating properties which can be used as a substitute for conventional solvents, in particular halogenated solvents.
The invention relates more particularly to a composition formed of branched carboxylic acid diesters which are obtained from a mixture of dinitriles. This mixture of dinitriles is obtained as distillation fraction during the recovery and purification of adiponitrile in the process for the manufacture of the latter compound by double hydrocyanation of butadiene.
An oxygenated solvent has been provided for several years. This solvent is based on diesters obtained by esterification of a mixture of dicarboxylic acids, more particularly of a mixture of adipic acid, glutaric acid and succinic acid. This mixture of acids is obtained in the process for the manufacture of adipic acid by oxidation of cyclohexanol and/or cyclohexanone.
This solvent, for example sold by Rhodia under the trade name Rhodiasolv RPDE or by Invista under the trade name DBE, is used in numerous applications, in particular as a replacement for hydrocarbon solvents, chlorinated solvents or oxygenated solvents (glycol ethers, acetone).
In addition to this technical performance, which is a result of its solvating power and of its physicochemical properties, this oxygenated solvent exhibits the advantage of being less damaging to the envirormient, of being biodegradable and of being easy to recycle. Its highly favourable toxicological profile makes it possible to eliminate any risk to the final user. In addition, the physicochemical properties, such as the low volatility and the flash point, allow it to be used in complete safety.
It can also be used as a mixture with other solvents, such as N-methylpyrrolidone (NMP), without affecting the solvent properties but while reducing the cost of this.
Furthermore, this solvent is stable at ambient temperature and exhibits a low

vapour pressure.
Oxygenated solvents exhibiting good solvating properties and without risk of toxicity and without danger to the environment are experiencing very strong growth. It is therefore important for the industrial sector to find and provide novel solvents exhibiting properties at least similar or equivalent to those of the solvents already available, such as the abovementioned RPDE.
One of the aims of the present invention is to provide a novel oxygenated solvent exhibiting physical properties, solvent properties, a toxicological profile and an ecotoxic impact which are similar or improved with respect to the solvent based on diesters of a mixture of adipic acid, glutaric acid and succinic acid.
To this end, the invention provides a novel composition comprising a mixture of diesters of ethylsuccinic acid, methylglutaric acid and optionally adipic acid.
According to another characteristic of the invention, this mixture comprises:
> from 70 to 95% by weight of methylglutaric acid diesters
> from 5 to 30% by weight of ethylsuccinic acid diesters
> from 0 to 10% by weight of adipic acid diesters
This composition is obtained starting from a mixture of dinitrile compounds in particular produced and recovered in the process for the manufacture of adipo-nitrile by double hydrocyanation of butadiene. This process, used on a large scale industrially to produce the great majority of adiponitrile consumed in the world, is described in numerous patents and works.
The reaction for the hydrocyanation of butadiene results predominantly in the formation of linear dinitriles but also in the formation of branched dinitriles, the two main ones of which are methylglutaronitrile and ethylsuccinonitrile.
In the stages of separation and purification of the adiponitrile, the branched dinitrile compounds are separated by distillation and recovered, for example as top fraction in a distillation column.

The invention provides for the conversion of this mixture of branched dinitrile compounds mto diesters in order thus to produce a novel solvent.
It can be of interest to eliminate more volatile compounds from the recovered branched dinitrile compounds by a simple distillation for example.
One of the possible processes for the conversion of dinitrile compounds to diesters corresponds to the use of the Pinner reaction, described in particular in French Patent No. 1 488 857. Basically, this process consists in reacting the dinitrile compounds with an alcohol in the presence of a strong inorganic acid, such as sulphvuric acid, and in then hydrolysing the products obtained in order to recover the diesters by distillation.
This document also describes a specific embodiment of the process which consists in passing the mixture of dinitrile compounds and the alcohol into a bath of molten salts based on various alkali metal and ammonium sulphates in order to prevent the formation of ammonium sulphate and to recover aqueous ammonia by extraction with steam.
The diesters of the invention can also be obtained by a reaction between the dinitrile compounds, water and an alcohol in the gas phase and in the presence of a solid catalyst. The reaction temperature is advantageously greater than the condensation temperature of the diesters formed. Use may be made, as catalyst, of a solid acid catalyst, such as, for example, a silica gel, a silica/alumina mixture, zeolites, zirconia or supported boric or phosphoric acids. Use may also be made of macroporous aluminas, such as those described in European Patent EP 0 805 801.
The temperature of the reaction is between 200 and 450°C, preferably between 230 and 350°C. The reaction can be carried out under any pressure, advantageously of between 0.1 and 20 bar. At the reactor outlet, the vapours are rapidly cooled to a temperature of less than or equal to 150°C. The ammonia, then the water and the alcohol in excess are separated by distillation from the mixture obtained.

The diesters of the invention can also be obtained by reaction between the dinitrile compounds and an inorganic base, in order to obtain acid salts, then neutralization of these salts by an acid, followed by esterification with an alcohol. Salts of diacids and in particular the ammonium salt of the diacids can be obtained by enzymatic hydrolysis of the nitrile compounds, such as described, for example, in Patents EP596812,FR2700777.
Finally, the diesters are purified according to purification processes conventionally used in the technical field of the preparation of organic compounds and in particular by distillation in one or more columns.
According to the invention, the mixture of diesters in accordance with the invention exhibits specific properties different from the properties of the mixture of diesters obtained by esterification of linear carboxylic acids. More particularly, it exhibits a crystallization temperature of less than -50°C, which makes possible use within a very broad temperature range with a low viscosity of the solvent.
By way of comparison, the solvent resulting from the mixture of linear carboxylic acids has a crystallization temperature of between -20°C and +20°C, depending on their composition.
The composition of the invention also exhibits a low solubility in water. Equally, the solubility of water in the composition is less than 2.5% by weight at 23°C.
The diesters forming the composition according to the invention are obtained by reaction of an alcohol with the abovementioned dinitrile compounds. Mention may be made, as alcohol which can be used for the manufacture of these compounds, of branched or unbranched and cyclic or acyclic aliphatic alcohols which can comprise an aromatic ring and which can comprise from 1 to 20 carbon atoms. Mention may be made, as preferred examples, of the following alcohols: methanol, propanol, isopropanol, benzyl alcohol, ethanol, n-butanol, isobutanol, pentanols, cyclohexanol, hexanol, isooctanol or 2-ethylhexanol.

f
The composition of the invention can be used alone or as a mixture with other solvents or with water in the form of a solution or emulsion. In particular, they can be used as a mixture with the diesters of the linear diacids mentioned above.
These compositions have applications as solvent in numerous fields, such as paints, varnishes and lacquers, the industry for coating surfaces or any other article, such as cables, for example, the ink industry, lubricants for textiles, binders and resins for foundry cores and moulds, cleaning products, cosmetic formulations, for the implementation of certain chemical reactions, in soil and plant treatment compositions and more generally the use, alone or in a formulation, as cleaning, pickling or degreasing solvent in any industrial or domestic activity. These compositions can also be used as plasticizers for some plastics or as monomers for the manufacture of polymers.
Other advantages or characteristics of the invention will be described in more detail and will be better illustrated in the light of the examples given below purely by way of illustration.
Example
43.26 g of a mixture A of dinitrile compounds are charged with 76.90 g of
methanol to a glass reactor with a capacity of 500 ml equipped with a vertical
reflux condenser and a stirrer and heated by an oil bath.
The mixture A of dinitrile compounds is composed of:
> 8 6.9% by weight of methylglutaronitrile
> 11.2% by weight of ethylsuccinonitrile
> 1.9% by weight of adiponitrile.
The remainder to 100% corresponds to the impurities present in this mixture,
which are generally not dinitrile compounds.
The dinitrile compounds/methanol mixture is cooled to approximately 1 °C before
the addition of 84.22 g of 98% by weight sulphuric acid.
The reaction medium is heated to reflux and is maintained at this temperature for
3 h. The reaction mass is heterogeneous and fluid. After cooling to 60°C, 63 g of
water are added. The reaction medium is maintained at 65°C for 2 hours.

117 g of additional water are then added. The reaction medium becomes two-phase. After removing the excess methanol by evaporation, the two phases are separated by settling and analysed. The organic phase recovered is washed with a saturated aqueous sodium chloride solution with addition of aqueous ammonia in order to obtain a pH in the region of 7.
Washing is carried out a second time with a saturated aqueous sodium chloride solution.

This mixture exhibits the following properties:
> Crystallization temperature (the crystallization point was determined by use of the method described in Standard NFT 20-051): less than -50°C
> Solubility with water:
0 Solubility of water in the composition: 2.2% by weight o Solubility of the composition in water: 2.5% by weight
This value was determined using a container equipped with a stirrer at a temperature of 23 °C, either by addition of water to 20 g of diester composition or by addition of the diester composition to 50 g of water, until a cloudy solution was obtained.
Resistance to hvdrolvsis:
Acidity is produced by adding 5 g of diester composition to 95 g of water comprising 8 millimol of NaOH. The flask is placed for several days in a chamber heated to 50°C.
The acidity of the medium is measured periodically in order to monitor the fall in

the pH.
These tests were carried out with the diester composition of the invention and, by way of comparison, with a diester composition resulting from a mixture of linear diacids sold by Rhodia under the trade name RPDE.
They show that the composition of the invention is more resistant to hydrolysis than the RPDE composition.
Likewise, comparative tests were carried out in order to evaluate the solvating power of the diesters of the invention in comparison with that of the RPDE composition of Rhodia.
These tests were carried out by mixing, in a container, resins commonly employed
in the painting field with a predetermined amount of solvent formed of diesters or
RPDE.
The results observed are listed in Tables I and II below:

The above tests show that the solvating power of the diesters of the invention is at least equivalent to that of the solvent RPDE.

CLAIMS
1. Composition comprising a mixture of diesters of ethylsuccinic acid and of methylglutaric acid.
2. Composition according to Claim 1, characterized in that it comprises diesters of adipic acid.
3. Composition according to either of Claims 1 and 2, characterized in that the concentration by weight of its various components is:

> diesters ofmethylglutaric acid ofbetween 70 and 95%
> diesters of ethylsuccinic acid of between 5 and 30%
> diesters of adipic acid of between 0 and 10%

4. Composition according to one of the preceding claims, characterized in that it exhibits a crystallization temperature of less than -50°C.
5. Composition according to one of the preceding claims, characterized in that the solubility of water in the said composition is less than or equal to 2.5% by weight at 23°C.
6. Composition according to one of the preceding claims, characterized in that it is obtained by esterification of corresponding dinitrile compounds.
7. Composition according to Claim 6, characterized in that the dinitrile compounds used are present in the mixture of the branched dinitriles which are separated from adiponitrile in the process for the manufacture of adiponitrile by double hydrocyanation of butadiene.
8. Composition according to one of the preceding claims, characterized in that the diesters are obtained by reaction of a dinitrile compound with an alcohol chosen from the group consisting of branched or unbranched and cyclic or acyclic aliphatic alcohols which can comprise an aromatic ring and which can comprise from 1 to 20 carbon atoms.

9. Composition according to Claim 8, characterized in that the alcohol is
chosen from the group consisting of methanol, propanol, isopropanol,
benzyl alcohol, ethanol, n-butanol, isobutanol, pentanols, cyclohexanol,
hexanol, isooctanol and 2-ethylhexanol.
10. Process for the manufacture of a diester composition according to one of
the preceding claims, characterized in that it consists in reacting a dinitrile
compound with an alcohol in the presence of a strong inorganic acid, in
then hydrolysing the medium and in recovering the diester composition.
11. Process for the manufacture of a diester composition according to one of
Claims 1 to 9, characterized in that it consists in reacting the dinitriles with
water and an alcohol in the gas phase in the presence of a solid catalyst.
12. Process according to Claim 11, characterized in that the catalyst is a solid
acid catalyst.
13. Process according to Claim 11, characterized in that the catalyst is a
macroporous alumina.
14. Process for the manufacture of a diester composition according to one of
Claims 1 to 9, characterized in that it consists in reacting the dinitriles with
a basic compound, in order to obtain acid salts, in neutralizing these salts
with an acid and in then esterifying the acids obtained by reaction with an
alcohol.
15. Use of a composition according to one of Claims 1 to 9 as solvent or
cosolvent.

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Patent Number

269845

Indian Patent Application Number

4709/CHENP/2008

PG Journal Number

46/2015

Publication Date

13-Nov-2015

Grant Date

11-Nov-2015

Date of Filing

05-Sep-2008

Name of Patentee

RHODIA OPERATIONS

Applicant Address

40 RUE DE LA HAIE-COQ, F-93306 AUBERVILLERS,

Inventors:

#	Inventor's Name	Inventor's Address
1	MARION, PHILIPPE,	140, ROUTE DU BUYE, F-69390 VERNAISON,
2	TOUILLET-FONTI, LISE,	64 RUE SAINTE ANNE DE BARABAN, F-69003 LYON,
3	BERNARD, JEAN-MARIE,	LIEUDIT LES MURES, 320 ROUTE DU LARGE, F-69440 SAINT- LAURENT D'AGNY,

PCT International Classification Number

C07C69/34

PCT International Application Number

PCT/FR07/00370

PCT International Filing date

2007-03-02

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	0602011	2006-07-07	France