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US3872138A - Process for the preparation of quaternary ammonium salts - Google Patents

Process for the preparation of quaternary ammonium salts Download PDF

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US3872138A
US3872138A US304128A US30412872A US3872138A US 3872138 A US3872138 A US 3872138A US 304128 A US304128 A US 304128A US 30412872 A US30412872 A US 30412872A US 3872138 A US3872138 A US 3872138A
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acid
alkyl
quaternary ammonium
carboxylic acid
carbon atoms
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US304128A
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Yuzuru Ogata
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Kao Corp
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38—Cationic compounds
    • C11D1/62—Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/62—Quaternary ammonium compounds
    • C07C211/63—Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/08—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions not involving the formation of amino groups, hydroxy groups or etherified or esterified hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/40—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton with quaternised nitrogen atoms bound to carbon atoms of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/02—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C219/04—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C219/06—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having the hydroxy groups esterified by carboxylic acids having the esterifying carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring

Definitions

  • ABSTRACT A quaternary ammonium salt containing an ester linkage in the cationic moiety is prepared by reacting an epihalohydrin with a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid.
  • a conventional method of preparing quaternary ammonium salts comprises reacting an alkyl amine with an alkyl halide. Re cently, methods using an epihalohydrin are adopted sometimes. The most typical method using an epihalohydrin comprises reacting an epihalohydrin directly with a tertiary amine. However, in this method it is difficult to prepare quaternary ammonium salts having a complicated structure. It is especially difficult to introduce a reactive group into the cationic moiety.
  • This invention is based on the discovery of a process for preparing quaternary ammonium salts having a reactive ester group in the cationic moiety, which are useful as textile-treating agents.
  • the products obtained by the process of this invention are useful as textilesoftening agents having an antistatic property, or as level-dycing or dyeing-retarding agents of the decomposition type.
  • this invention is to provide a process for the preparation of quaternary ammonium salts having an ester linkage in the cationic moiety, characterized by reacting an epihalohydrin with a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid.
  • the salt of an alkyl tertiary amine and a carboxylic acid may be prepared in an ordinary solvent such as benzene and lower aliphatic alcohols by a customary method.
  • the kind ofthe epihalohydrin is appropriately chosen depending on whether the intended quaternary ammonium salt is a chloride or bromide.
  • Quaternary ammonium salts to be obtained by the process of the present invention are represented by a chemical formula as follows:
  • R is an alkyl, alkenyl or cycloalkyl radical of from 1 to 17 carbon atoms; in which N is a quaternary nitrogen atom; in which X is halogen, such as chlorine, bromine and fluorine; and in which each of R,, R and R is an alkyl or alkenyl radical having 1 to 18 carbon atoms.
  • alkyl or alkenyl tertiary amines which may be quaternized in the practice ofthe present invention are as follows:
  • Epihalohydrin for example, epichlorohydrin or epibromohydrin.
  • carboxylic acids which may be used in the practice of the present invention are as follows:
  • Our process involves the preparation of a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid by neutralizing the carboxylic acid with the amine in substantially stoichiometric amounts. Then, the salt is re acted with epihalohydrin.
  • the reaction may be carried out at any suitable temperature and pressure, temperatures between 50C and C and pressures at or near atmospheric being suitable. Conveniently, the reaction is carried out in the presence of a solvent such as benzene and a lower aliphatic alcohol, for example, methanol, ethanol, propanol, butanol, pentanol, etc.
  • the temperature of the reaction may be very conveniently controlled by conducting the reaction under reflux conditions. We have found that the use of benzene is highly satisfactory.
  • Epihalohydrin can be used in a substantially stoichiometric amount, but it may be preferably employed in a slight excess, for example, 20 percent excess over its stoichiometric amount.
  • the solvent employed is first distilled off. Purification is largely by way of removal of small quantities of unreacted reactants by any suitable means such as extraction with a suitable solvent, for example, diethyl ether and/or recrystallization from a suitable solvent, for example, acetone and diethyl ether.
  • a suitable solvent for example, diethyl ether and/or recrystallization from a suitable solvent, for example, acetone and diethyl ether.
  • tertiary amine is selected from the group consisting of trimethylamine, triethylamine, trinormalpropylamine, dimethylethylamine, methyldiethylamine, dimethylallylamine, diethyallylamine, dimethyldodecylamine, dimethyloctadecylamine, trioctylamine, trioctadecylamine and trioleylamine and mixtures thereof and said carboxylic acid is selected from the group consisting of acetic acid, lauric acid, crotonic acid, acrylic acid, methacrylic acid, oleic acid, l-adamantyl carboxylic acid and cyclohexyl carboxylic acid.
  • each of R R and R is alkyl having 1 to 18 carbon atoms and R is selected from the group consisting of alkyl having 1 to 17 carbon atoms, alkenyl having from 2 to 17 carbon atoms, adamantyl and cyclohexyl.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

A quaternary ammonium salt containing an ester linkage in the cationic moiety is prepared by reacting an epihalohydrin with a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid.

Description

United States Patent [191 Ogata 1 PROCESS FOR THE PREPARATION OF QUATERNARY AMMONIUM SALTS [75] Inventor: Yuzuru Ogata, Wakayama, Japan [73] Assignee: Kao Soap Co., Ltd., Tokyo, Japan [22] Filed: Nov. 6, 1972 [21] Appl. No.: 304,128
[30] Foreign Application Priority Data UNITED STATES PATENTS 3,272,712 9/1966 Kalopissis et a1. 260/404 X 1 Mar. 18, 1975 3,290,304 12/1966 Kalopissis et al. 260/404 X 3,383,397 5/1968 Milks et a1 260/404 3,514,473 5/1970 McFadden et a1, 260/486 R 3,694,393 9/1972 Lewis et al 260/486 R Primary ExaminerLewis Gotts Assistant Examiner-Ethel G. Love Attorney, Agent, or FirmWo0dhams, Blanchard and Flynn [57] ABSTRACT A quaternary ammonium salt containing an ester linkage in the cationic moiety is prepared by reacting an epihalohydrin with a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid.
5 Claims, No Drawings PROCESS FOR THE PREPARATION OF QUATERNARY AMMONIUM SALTS BACKGROUND OF THE INVENTION This invention relates to a new process for preparing quaternary ammonium salts which are useful as detergents, emulsifying agents and wetting agents, particularly as textile treating agents.
DESCRIPTION OF THE PRIOR ART A conventional method of preparing quaternary ammonium salts, which is usually adopted in the art, comprises reacting an alkyl amine with an alkyl halide. Re cently, methods using an epihalohydrin are adopted sometimes. The most typical method using an epihalohydrin comprises reacting an epihalohydrin directly with a tertiary amine. However, in this method it is difficult to prepare quaternary ammonium salts having a complicated structure. It is especially difficult to introduce a reactive group into the cationic moiety.
As disclosed in US. Pat. Nos. 2,547,965 or 2,548,679, it has been known that when an adduct of a tertiary amine with an alkyl phenol or mercaptan synthesized in advance is quaternarized by an epihalohy drin, the alkyl phenol or mercaptan is introduced in the cationic moiety in the form of a phenyl ether or thioether. However, since the linkage introduced into the cationic moiety is an ether linkage, its reactivity is relatively low. Also, a method comprising synthesizing in advance a salt of a tertiary amine with a mineral acid such as hydrochloric acid and then reacting an epihalohydrin with the salt has been known in the art. However, according to this method it is impossible to introduce a reactive group into the cationic moiety.
DETAILED DESCRIPTION This invention is based on the discovery of a process for preparing quaternary ammonium salts having a reactive ester group in the cationic moiety, which are useful as textile-treating agents. The products obtained by the process of this invention are useful as textilesoftening agents having an antistatic property, or as level-dycing or dyeing-retarding agents of the decomposition type.
More specifically, this invention is to provide a process for the preparation of quaternary ammonium salts having an ester linkage in the cationic moiety, characterized by reacting an epihalohydrin with a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid.
The salt of an alkyl tertiary amine and a carboxylic acid may be prepared in an ordinary solvent such as benzene and lower aliphatic alcohols by a customary method. The kind ofthe epihalohydrin is appropriately chosen depending on whether the intended quaternary ammonium salt is a chloride or bromide.
Quaternary ammonium salts to be obtained by the process of the present invention are represented by a chemical formula as follows:
i R1 til ca claca ofi R x' R3 on in which R is an alkyl, alkenyl or cycloalkyl radical of from 1 to 17 carbon atoms; in which N is a quaternary nitrogen atom; in which X is halogen, such as chlorine, bromine and fluorine; and in which each of R,, R and R is an alkyl or alkenyl radical having 1 to 18 carbon atoms.
In the production of these compounds, the following three reactants are used:
I. An alkyl or alkenyl tertiary amine having the formula wherein each of R R and R is an alkyl or alkenyl rad ical having 1 to 18 carbon atoms.
Some examples of alkyl or alkenyl tertiary amines which may be quaternized in the practice ofthe present invention are as follows:
Trimethylamine, triethylamine, trinormalpropylamine, dimethylethylamine, methyldiethylamine, dimethylallylamine, diethylallylamine, dimethyldodecylamine, dimethyloctadecylaminc, trioctylamine, trioctadecylamine and trioleylamine and mixtures thereof.
2. Epihalohydrin, for example, epichlorohydrin or epibromohydrin.
3. A saturated or unsaturated aliphatic carboxylic acid, or alicyclic acid having from 2 to 18 carbon atoms and represented by the formula of RCOOH, wherein R is an alkyl, alkenyl or cycloalkyl radical such as cyclohexyl and adamantyl having from 1 to 17 carbon atoms.
Some examples of carboxylic acids which may be used in the practice of the present invention are as follows:
Acetic acid, lauric acid, crotonic acid, acrylic acid, methacrylic acid, oleic acid, l-adamantyl carboxylic acid and cyclohexyl carboxylic acid.
Our process involves the preparation of a salt of an alkyl or alkenyl tertiary amine and a carboxylic acid by neutralizing the carboxylic acid with the amine in substantially stoichiometric amounts. Then, the salt is re acted with epihalohydrin. The reaction may be carried out at any suitable temperature and pressure, temperatures between 50C and C and pressures at or near atmospheric being suitable. Conveniently, the reaction is carried out in the presence of a solvent such as benzene and a lower aliphatic alcohol, for example, methanol, ethanol, propanol, butanol, pentanol, etc. The temperature of the reaction may be very conveniently controlled by conducting the reaction under reflux conditions. We have found that the use of benzene is highly satisfactory.
Epihalohydrin can be used in a substantially stoichiometric amount, but it may be preferably employed in a slight excess, for example, 20 percent excess over its stoichiometric amount.
After the reaction, the solvent employed is first distilled off. Purification is largely by way of removal of small quantities of unreacted reactants by any suitable means such as extraction with a suitable solvent, for example, diethyl ether and/or recrystallization from a suitable solvent, for example, acetone and diethyl ether.
Our process has outstanding advantages in that the highly desirable quaternary compounds may be we pared in excellent yield and quality, from available and relatively inexpensive raw materials, by a simple method and with the use of conventional equipment.
This invention will now be illustrated more detailedly with reference to Examples.
EXAMPLE 1 25.8 g (0.3 mole) of crotonic acid was dissolved in 150 g of benzene, and the solution was neutralized by addition of 30.4 g (0.3 mole) of triethylamine. Then, 33.4 g (0.36 mole) of epichlorohydrin was added to the solution, and the reaction was conducted at 80C. for 15 hours. After completion of the reaction, benzene was distilled off under reduced pressure and unreacted reactants contained in the residue were removed by extraction with diethyl ether to obtain 50.4 g of a grayish brown, jelly-like product having a structure expressed by the following formula (I):
(c 11 ucn cn CH2-O(IIICH-CHCH3] c2 (I) The yield was 60 percent, and results of the analysis are as follows:
Found Calculatcd Values Values N 4.8% 5.0% CI 12.7% 12.7% CI 12.0% 12.7% hydroxyl number 210 200 suponification number 200 200 EXAMPLE 2 50.1 g (0.25 mole) of lauric acid was dissolved in 80 g of benzene, and neutralization was accomplished by addition of 25.3 g (0.25 mole) of triethylamine. Then, 27.8 g (0.3 mole) of epichlorohydrin was added to the neutralized product and the reaction was conducted at 80C. for 15 hours. Purification were carried out in the same manner as in Example 1 to obtain 45.4 g of a faintly yellow, transparent, viscous liquid product having a structure expressed by the following formula (11), the yield being 46%:
27 g (0.15 mole) of l-adamantyl carboxylic acid was dissolved in 80 g of benzene, and it was neutralized by addition of 32 g (0.15 mole) of dimethyl ndodecylamine. Then, 16.7 g (0.18 mole) of epichlorohydrin was added to the neutralized product, and the reaction was conducted at 80C. for 15 hours. After completion of the reaction, benzene was distilled off under reduced pressure and a large excess of diethyl ether was added to the residue, then the mixture was cooled to precipitate crystals. Thus, there was obtained 34.7 g of a white powdery product having a structure expressed by the following formula (III) and melting at 132.5C., the yield being 47.6%:
C H IiICH (|ZHCH O(|I|-Ad C9, (111) CH 0a 0 Ad adamantyl residue Results of the elementary analysis are as follows:
Found Values Calculated Values EXAMPLE 4 C H IIICH CIIHCI-I OCHCH C2. (IV) Cl-I OH O Results of the elementary analysis are as follows:
Found Values Calculated Values EXAMPLE 5 53.3 g (0.25 mole) of dimethyl n-dodecylamine was dissolved in g of benzene, and it was neutralized by addition of 15 g (0.25 mole) of acetic acid. Then, 27.8 g (0.30 mole) of epichlorohydrin was added to the neutralized product and the reaction was conducted at 80C. for hours. After completion of the reaction, purification was carried out in the same manner as in Example 1 to obtain 88.4 g of a brown viscous liquid product having a structure expressed by the following formula (V), the yield being 96.5%:
: CH C H IiCH CHCH 0tfiCH c2 CH OH 0 Results of the analysis are as follows:
Found Calculated Values Values N 3.971 3,871 Cl 10.0% 9.7% CI 9,571 9.7% hydroxyl number 160 153 saponification number 155 153 The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
l. A process for preparing quaternary ammonium salts containing an ester linkage in the cationic moiety, of the formula i R 1|? CH ICHCH OE R X R3 OH O M in which R is alkyl, alkenyl or cycloalkyl having 1 to 17 carbon atoms, X is halogen and each of R R and R is alkyl or alkenyl having 1 to 18 carbon atoms which comprises neutralizing a carboxylic acid of the formula-RCOOH with a substantially stoichiometric amount ofa tertiary amine of the formula to form a salt and then reacting said salt with a stoi' chiometric amount or a slight excess of an cpihalohydrin to form a compound of the first-mentioned formula.
2. A process according to claim 1, in which the reaction is carried out at a temperature of 50 to C in the presence of a solvent.
3. A process according to claim 1, in which said tertiary amine is selected from the group consisting of trimethylamine, triethylamine, trinormalpropylamine, dimethylethylamine, methyldiethylamine, dimethylallylamine, diethyallylamine, dimethyldodecylamine, dimethyloctadecylamine, trioctylamine, trioctadecylamine and trioleylamine and mixtures thereof and said carboxylic acid is selected from the group consisting of acetic acid, lauric acid, crotonic acid, acrylic acid, methacrylic acid, oleic acid, l-adamantyl carboxylic acid and cyclohexyl carboxylic acid.
4. The process of claim 3, in which said epihalohydrin is epichlorohydrin.
5. A process according to claim 1, in which each of R R and R is alkyl having 1 to 18 carbon atoms and R is selected from the group consisting of alkyl having 1 to 17 carbon atoms, alkenyl having from 2 to 17 carbon atoms, adamantyl and cyclohexyl.

Claims (5)

1. A PROCESS FOR PREPARING QUATERNARY AMMONIUM SALTS CONTAINING AN ESTER LINKAGE IN THE CATIONIC MOIETY, OF THE FORMULA
2. A process according to claim 1, in which the reaction is carried out at a temperature of 50* to 150*C in the presence of a solvent.
3. A process according to claim 1, in which said tertiary amine is selected from the group consisting of trimethylamine, triethylamine, trinormalpropylamine, dimethylethylamine, methyldiethylamine, dimethylallylamine, diethyallylamine, dimethyldodecylamine, dimethyloctadecylamine, trioctylamine, trioctadecylamine and trioleylamine and mixtures thereof and said carboxylic acid is selected from the group consisting of acetic acid, lauric acid, crotonic acid, acrylic acid, methacrylic acid, oleic acid, 1-adamantyl carboxylic acid and cyclohexyl carboxylic acid.
4. The process of claim 3, in which said epihalohydrin is epichlorohydrin.
5. A process according to claim 1, in which each of R1, R2 and R3 is alkyl having 1 to 18 carbon atoms and R is selected from the group consisting of alkyl having 1 to 17 carbon atoms, alkenyl having from 2 to 17 carbon atoms, adamantyl and cyclohexyl.
US304128A 1971-11-09 1972-11-06 Process for the preparation of quaternary ammonium salts Expired - Lifetime US3872138A (en)

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3992304A (en) * 1975-02-10 1976-11-16 Kao Soap Co., Ltd. Softening agent for a woven fabric
US4339391A (en) * 1979-07-14 1982-07-13 Hoechst Aktiengesellschaft Quaternary ammonium compounds
US4368127A (en) * 1979-07-02 1983-01-11 Akzona Incorporated Fabric softening compounds and method
US4621141A (en) * 1984-04-26 1986-11-04 Mobil Oil Corporation Additives for improving low temperature characteristics of fuels and method for use thereof
US4840738A (en) * 1988-02-25 1989-06-20 The Procter & Gamble Company Stable biodegradable fabric softening compositions containing 2-hydroxypropyl monoester quaternized ammonium salts
US5422021A (en) * 1989-09-19 1995-06-06 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening
US5516438A (en) * 1989-09-19 1996-05-14 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening
FR2756823A1 (en) * 1996-12-11 1998-06-12 Oreal PROCESS FOR THE PREPARATION OF HYDROXYPROPYL QUATERNARY AMMONIUMS DERIVED WITH ESTER FUNCTION OF FATTY ACID
EP0918104A1 (en) * 1997-11-19 1999-05-26 Arizona Chemical Oy A papermaking process and a cationic chemical
US6214325B1 (en) 1996-12-11 2001-04-10 L'oreal Hydroxypropyl quaternary ammonium compounds containing an ester function, and cosmetic and dermatological compositions containing them
US6521782B1 (en) * 1999-01-21 2003-02-18 Atofina Method for making aqueous solutions of unsaturated quaternary ammonium salts

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59184897U (en) * 1983-05-27 1984-12-08 株式会社　タカラ traveling toy
IT1249056B (en) * 1991-05-22 1995-02-11 Donegani Guido Ist LIQUID CATALYSTS FOR THE QUICK POLYMERISATION OF LIQUID COMPOSITIONS BASED ON POLYISOCYANATES AND EPOXY.

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US3272712A (en) * 1962-10-29 1966-09-13 Oreal Quaternary ammonium salts of esters of fatty acids and a precursor of amino-2-hydroxy propanol, methods of their preparation and their use
US3290304A (en) * 1961-11-02 1966-12-06 Oreal Quaternary ammonium compounds, their preparation and their use
US3383397A (en) * 1965-01-14 1968-05-14 Arizona Chem 3-amino-2-hydroxypropyl esters and methods for preparing the same
US3514473A (en) * 1967-08-02 1970-05-26 Dow Chemical Co Aminohydroxyalkyl methacrylates
US3694393A (en) * 1969-04-04 1972-09-26 Rohm & Haas Method of producing paper,and paper obtained

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US3397227A (en) * 1967-11-09 1968-08-13 Shell Oil Co Ester production

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Publication number Priority date Publication date Assignee Title
US3290304A (en) * 1961-11-02 1966-12-06 Oreal Quaternary ammonium compounds, their preparation and their use
US3272712A (en) * 1962-10-29 1966-09-13 Oreal Quaternary ammonium salts of esters of fatty acids and a precursor of amino-2-hydroxy propanol, methods of their preparation and their use
US3383397A (en) * 1965-01-14 1968-05-14 Arizona Chem 3-amino-2-hydroxypropyl esters and methods for preparing the same
US3514473A (en) * 1967-08-02 1970-05-26 Dow Chemical Co Aminohydroxyalkyl methacrylates
US3694393A (en) * 1969-04-04 1972-09-26 Rohm & Haas Method of producing paper,and paper obtained

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3992304A (en) * 1975-02-10 1976-11-16 Kao Soap Co., Ltd. Softening agent for a woven fabric
US4368127A (en) * 1979-07-02 1983-01-11 Akzona Incorporated Fabric softening compounds and method
US4339391A (en) * 1979-07-14 1982-07-13 Hoechst Aktiengesellschaft Quaternary ammonium compounds
EP0022562B1 (en) * 1979-07-14 1985-06-19 Hoechst Aktiengesellschaft Quaternary ammonium compounds, their preparation and their use as fabric softener
US4621141A (en) * 1984-04-26 1986-11-04 Mobil Oil Corporation Additives for improving low temperature characteristics of fuels and method for use thereof
EP0330261A3 (en) * 1988-02-25 1990-12-27 The Procter & Gamble Company Stable biodegradable fabric softening compositions containing 2-hydroxypropyl monoester quaternized ammonium salts
US4840738A (en) * 1988-02-25 1989-06-20 The Procter & Gamble Company Stable biodegradable fabric softening compositions containing 2-hydroxypropyl monoester quaternized ammonium salts
US5422021A (en) * 1989-09-19 1995-06-06 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening
US5516438A (en) * 1989-09-19 1996-05-14 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening
FR2756823A1 (en) * 1996-12-11 1998-06-12 Oreal PROCESS FOR THE PREPARATION OF HYDROXYPROPYL QUATERNARY AMMONIUMS DERIVED WITH ESTER FUNCTION OF FATTY ACID
EP0847985A1 (en) * 1996-12-11 1998-06-17 L'oreal Process for the preparation of fatty acid esters of hydroxypropylated quaternary ammonium derivatives
US6046344A (en) * 1996-12-11 2000-04-04 L'oreal Process for the preparation of hydroxypropylated quaternary ammonium compounds containing an ester functional group
US6214325B1 (en) 1996-12-11 2001-04-10 L'oreal Hydroxypropyl quaternary ammonium compounds containing an ester function, and cosmetic and dermatological compositions containing them
EP0918104A1 (en) * 1997-11-19 1999-05-26 Arizona Chemical Oy A papermaking process and a cationic chemical
US6521782B1 (en) * 1999-01-21 2003-02-18 Atofina Method for making aqueous solutions of unsaturated quaternary ammonium salts

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Publication number Publication date
GB1390534A (en) 1975-04-16
JPS5229292B2 (en) 1977-08-01
JPS4852716A (en) 1973-07-24

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