GB771635A - Amphoteric surface-active organic compounds and process of preparing same - Google Patents

Amphoteric surface-active organic compounds and process of preparing same

Info

Publication number
GB771635A
GB771635A GB14496/55A GB1449655A GB771635A GB 771635 A GB771635 A GB 771635A GB 14496/55 A GB14496/55 A GB 14496/55A GB 1449655 A GB1449655 A GB 1449655A GB 771635 A GB771635 A GB 771635A
Authority
GB
United Kingdom
Prior art keywords
give
cresol
methyl
dodecyl
chloro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB14496/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Evonik Operations GmbH
Original Assignee
TH Goldschmidt AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by TH Goldschmidt AG filed Critical TH Goldschmidt AG
Priority to GB14496/55A priority Critical patent/GB771635A/en
Publication of GB771635A publication Critical patent/GB771635A/en
Expired legal-status Critical Current

Links

Abstract

The invention comprises amphoteric surface-active agents which yield soluble surface-active salts in presence of acids and bases of the formula <FORM:0771635/IV(b)/1> wherein xis an integer from 1 to 3, y ranges from 0 to 3, but x+y is not greater than 5, R1 is alkyl or alkaryl of 8-18 carbon atoms, A is a divalent group of formula: -NR3-, -NR3-(C2H4NH)z-, or -NR3-(C3H6NH)z (Z being 1 to 3, R3 representing H or alkyl of 8-18 carbon atoms), R2 is methyl, ethyl, propyl, halogen, carboxyl, or the group <FORM:0771635/IV(b)/2> They are bactericides (see Group VI) and are made by reacting at elevated temperatures an amine of formula R1-A-H with formaldehyde and with a phenol of the formula <FORM:0771635/IV(b)/3> the molecular proportions of amine and formaldehyde being about 1 : 1, while the molecular proportions of amine to phenol are from about 1 : 1 to 3 : 1 according to the number of R1-A-CH2- groups in the compound to be produced. In examples: formaldehyde is reacted with (1) octylamine and phenol to give o- and p-octylaminomethylphenol, (2) dodecyl-diethylene triamine and phenol to give o- and p-dodecyl-diethylene-triamine-methylphenol; (3) dodecyl-diethylenetriamine and p-chloro-m-cresol to give o - dodecyl - diethylenetriaminomethyl - p - chloro - m - cresol; (4) octyl - diethylenetriamine and p-cresol to give o-octyldiethylene-triamino - methyl - p - cresol; (5) octyl - diethylene-triamine and p-chloro-m-xylenol to give o - octyl - diethylenetriamine - methyl - p - chloro - m - xylenol; (6) p - dodecylbenzyl-triethylene-tetramine and phenol to give p-dodecylbenzyl - triethylenetetramino - methyl - o-or -p-hydroxybenzene; (7) tetradecylamine and phenol to give bis-tetradecylaminomethyl-phenol; (8) octyldiethylenetriamine and p-cresol to give bis-(o-octyl-diethylenetriaminomethyl)-p-cresol; (9) dodecyldiethylenetriamine and p-chloro-m-cresol to give bis-(o-dodecyl-diethylenetriamino-methyl)-p-chloro-m-cresol; (10) dodecyl - diethylenetriamine and salicylic acid or p-hydroxy-benzoic acid to give 3,5-bis-(dodecyl - diethylenetriaminomethyl) - salicylic acid or p-hydroxy-benzoic acid; (11) dodecyl-diethylenetriamine and 2,2-bis-(4,4-dioxy-diphenyl)-propane to give 2,2-bis-(p-hydroxy-m,m - di - (dodecyldiethylene - triaminomethyl)-phenyl)-propane.ALSO:Bactericidal compositions comprise aqueous solutions of acid salts (e.g. formic, acetic, or lactic salts) of compounds of the formula:- <FORM:0771635/VI/1> where in x is an integer from 1 to 3, y ranges from 0 to 3, but x + y is not greater than 5, R1 is alkyl or alkaryl of 8-18 carbon atoms, A is a divalent group of formula:-NR3-, -NR3-(C2 H4 NH)z, or -NR3-(C3 H6 NH) z - (z being 1 to 3, and R3 representing H or alkyl of 8-18 carbon atoms), R2 is methyl, ethyl, propyl, halogen, carboxyl, or the group:- <FORM:0771635/VI/2> The concentration of the salt may be 5-25 per cent. Compounds of the above formula which are specified include o- and p-octylaminomethylphenol, o- and p-dodecyldiethylenetriamino - methylphenol, o - dodecyldiethylenetriamino - methyl - p - chloro -m-cresol, o - octyldiethylenetriamino - methyl - p - cresol, o - octyl - diethylenetriamino - methyl - p - chloro - m - xylenol Others are listed.
GB14496/55A 1955-05-19 1955-05-19 Amphoteric surface-active organic compounds and process of preparing same Expired GB771635A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB14496/55A GB771635A (en) 1955-05-19 1955-05-19 Amphoteric surface-active organic compounds and process of preparing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB14496/55A GB771635A (en) 1955-05-19 1955-05-19 Amphoteric surface-active organic compounds and process of preparing same

Publications (1)

Publication Number Publication Date
GB771635A true GB771635A (en) 1957-04-03

Family

ID=6679131

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14496/55A Expired GB771635A (en) 1955-05-19 1955-05-19 Amphoteric surface-active organic compounds and process of preparing same

Country Status (1)

Country Link
GB (1) GB771635A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3161612A (en) * 1959-04-15 1964-12-15 Bayer Ag Alkylated amino phenols protecting rubber goods against ozone
US3400154A (en) * 1965-07-26 1968-09-03 Dow Chemical Co Alkylidene bis
US3413347A (en) * 1966-01-26 1968-11-26 Ethyl Corp Mannich reaction products of high molecular weight alkyl phenols, aldehydes and polyaminopolyalkyleneamines
FR2556013A1 (en) * 1983-12-03 1985-06-07 Sandoz Sa PROCESS FOR POST-PROCESSING TINTED OR PRINTED CELLULOSIC SUBSTRATES
CN110627662A (en) * 2019-09-23 2019-12-31 山东益丰生化环保股份有限公司 Detergent dispersant and oil slurry scale inhibitor containing same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3161612A (en) * 1959-04-15 1964-12-15 Bayer Ag Alkylated amino phenols protecting rubber goods against ozone
US3400154A (en) * 1965-07-26 1968-09-03 Dow Chemical Co Alkylidene bis
US3413347A (en) * 1966-01-26 1968-11-26 Ethyl Corp Mannich reaction products of high molecular weight alkyl phenols, aldehydes and polyaminopolyalkyleneamines
FR2556013A1 (en) * 1983-12-03 1985-06-07 Sandoz Sa PROCESS FOR POST-PROCESSING TINTED OR PRINTED CELLULOSIC SUBSTRATES
CN110627662A (en) * 2019-09-23 2019-12-31 山东益丰生化环保股份有限公司 Detergent dispersant and oil slurry scale inhibitor containing same

Similar Documents

Publication Publication Date Title
GB771635A (en) Amphoteric surface-active organic compounds and process of preparing same
US2278499A (en) Amine salts
GB871930A (en) Process for preparing symmetrical and unsymmetrical carbocyanine dyes and merocarbocyanine dyes
ES400824A1 (en) Amidinocarbamates
GB1489803A (en) Aminoacetamides and a process for their preparation
US4071543A (en) Process for the preparation of acyltaurides
GB1047061A (en) Polymers and a process for the preparation thereof
ES296381A1 (en) Procedure for the obtaining of new polybasic compounds (Machine-translation by Google Translate, not legally binding)
GB481733A (en) Improvements in or relating to vermin destroying bactericidal, insecticidal and likecompositions and the production thereof
GB759331A (en) Manufacture of basic polyglycol ethers and their use
GB680952A (en) Improvements in new morphine derivatives and production thereof
GB998264A (en) Herbicidal compositions
US2744902A (en) Alkyl naphthyl quaternary ammonium compounds
GB733732A (en) Improvements in or relating to new mercurated organic compounds and process of preparing the same
GB774679A (en) Manufacture of new bactericidal and fungicidal compounds and preparations containingthem
US2048821A (en) Manufacture of substituted acid amides
JPS55139346A (en) Preparation of bis(8-guanidinooctyl)amine acetic acid salt
GB744926A (en) Polyhydroxyamino acid compounds
GB1467107A (en) N,n-dimethyl-n-o-phenyl-thiono-alkane-phosphonyl-formamidines a process for their preparation and their use as insecticides acaricid3s and nematocides
GB884206A (en) 4-alkoxymetanilamides and compositions containing them
GB744941A (en) Improvements in or relating to sodium nitrate and compositions containing it
GB744281A (en) Improvements in and relating to pyridine derivatives and the manufacture thereof
GB723317A (en) Di-alkyl substituted alkylene polyamino acetic acids
GB496004A (en) Alkanol-amine salts of mandelic acid and process for producing them
GB679894A (en) Production of thiosemicarbazones