GB963907A - Compositions including a phenolic component and a polyamine component - Google Patents

Compositions including a phenolic component and a polyamine component

Info

Publication number
GB963907A
GB963907A GB38631/60A GB3863160A GB963907A GB 963907 A GB963907 A GB 963907A GB 38631/60 A GB38631/60 A GB 38631/60A GB 3863160 A GB3863160 A GB 3863160A GB 963907 A GB963907 A GB 963907A
Authority
GB
United Kingdom
Prior art keywords
radical
dichlorophenol
triamine
lauryl
groups
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
GB38631/60A
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.)
NICHOLAS MILKOS MOLNAR
Original Assignee
NICHOLAS MILKOS MOLNAR
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 NICHOLAS MILKOS MOLNAR filed Critical NICHOLAS MILKOS MOLNAR
Publication of GB963907A publication Critical patent/GB963907A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02Amines; Quaternary ammonium compounds
    • A01N33/04Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/20Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof

Abstract

A germicidal composition useful for the degerming of skin hair, scalp, oral and other body openings comprises combinations of anionic and cationic substances whereof the anionic component is phenolic and the cationic component is a derivative of an alkylene polyamine. The cationic component may be (1) N-alkylated or alkenylated alkylene polyamines which possess at least one of said aliphatic hydrocarbon groups having from 6 to 20 carbon atoms joined to one of the amino nitrogen groups and having one to five alkylene groups interconnected by nitrogen atoms and represented structurally as follows: X-NH-R-(NH-R)n-NY1Y2 in which R is an alkylene radical which may be the ethylene radical (-CH2CH2-), the isopropylene radical [-CCH2CH(CH3)-], the trimethylene radical (-CH2CH2CH2-), or a mixture of such radicals and "n" may be zero, in which case the parenthesized group is non-existent or "n" may be a whole number from 1 to 4; and X is an alkyl or alkenyl radical which may have from one to twenty carbon atoms, e.g. in the alkyls in the range from methyl or eicosyl (C20H41-) and Y1 and Y2 are hydrogen atoms or alkyl or alkenyl or carboxyalkyl or carboxy alkenyl groups having from 1 to 20 carbon atoms in the aliphatic hydrocarbon radical or (2) Acylamidoalkylene polyamines wherein the acyl group has from 2 to 20 carbon atoms joined through the carbonyl group to one of the amino nitrogen groups and having one to five alkylene groups interconnected by nitrogen atoms, and may be represented structurally as follows: <FORM:0963907/A5-A6/1> in which the symbols "X", "R," "Y1" and "Y2" and "n" are as already defined. The anionic components are: 1. Simple phenolics, such as: phenol, cresol, O-phenylphenol and the halogenated phenolics, such as p-chloro-meta-xylenol, dichloro-metaxylenol, o-benzyl p-chlorophenol and p-isoamylphenol. 2. Bis-phenolics, e.g.: 2,21-methylene bis-(3,4,6-trichlorophenol), 2,21-methylene bis-(4,6-dichlorophenol), 2,21-methylene bis-(4-chlorophenol), 2,21-thio bis-(4,6-dichlorophenol). 3. Salicylanilides, e.g. salicylanilide, monohalogenated salicylanilides, polyhalogenated salicylanilides. Also included among the aforesaid anionics are halogenated carbanilides and thiocarbanilides. Specified combinations are hexachlorophene and lauryl diethylene triamine, lauroylamido diethylene diamine and 2,21-thio bis-(4,6-dichlorophenol); dimethylamino propyl lauramide and o-benzyl-p-chlorophenol; dimethylamino propyl stearamide and 2,21-methylene bis-(4,6-dichlorophenol); lauryl diethylene triamine and 3,4,41-trichloro-carbanilide; lauryl diethylene triamine and 3,31, 41, 5-tetrachlorosalicylanilide; stearyl triethylene tetramine and 41,5 - dibromsalicylanilide, tetrachlorosalicylanilide and lauryldiethylene triamine; 41,5-dichlorosalicylanilide and lauryldiethylene triamine; laurylamide ethylene diamine and 2,21-methylene bis - (3,4,6 - trichlorophenol); dimethylamino propyl lauramide and 2, 21-thiobis - (41,6 - dichlorophenol); lauryl diethylamine triamine and 4,51 - dibromo - salicylanilide lauryl triethylene tetramine and 3,31,41,5-tetrachlorosalicylanilide and laurylethylene diamine and 3, 4, 41-trichlorocarbanalide. U.S.A. Specification 2,267,204 and German Specification 1,041,627 are referred to.
GB38631/60A 1959-11-12 1960-11-10 Compositions including a phenolic component and a polyamine component Expired GB963907A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US852172A US3108036A (en) 1959-11-12 1959-11-12 Germicidal compositions

Publications (1)

Publication Number Publication Date
GB963907A true GB963907A (en) 1964-07-15

Family

ID=25312649

Family Applications (1)

Application Number Title Priority Date Filing Date
GB38631/60A Expired GB963907A (en) 1959-11-12 1960-11-10 Compositions including a phenolic component and a polyamine component

Country Status (5)

Country Link
US (1) US3108036A (en)
CH (1) CH409250A (en)
GB (1) GB963907A (en)
NL (2) NL257911A (en)
SE (1) SE313891B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3717579A (en) * 1970-10-05 1973-02-20 Goldschmidt Ag Th Biocidal preparation
WO1984000006A1 (en) * 1982-06-18 1984-01-05 Bucuresti Medicamente Anti-tumour pharmaceutical preparation

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3391144A (en) * 1961-10-06 1968-07-02 Dow Chemical Co Subustituted phenyl alpha-(3-glutar-imidyl) acetates
US3285923A (en) * 1963-07-03 1966-11-15 Millmaster Onyx Corp Alkyl isoquinolinium phenates
US3485919A (en) * 1963-09-05 1969-12-23 Procter & Gamble Antibacterial composition
US3475540A (en) * 1963-09-05 1969-10-28 S E Massengill Co The Synergistic antimicrobial compositions
US3324178A (en) * 1964-01-06 1967-06-06 Allied Chem Biologically active n-hexahalohydroxyisopropyl amides
US3912816A (en) * 1970-02-27 1975-10-14 Goldschmidt Ag Th Certain bactericidal triamine
US3940482A (en) * 1971-04-21 1976-02-24 Colgate-Palmolive Company Solubilization of the zinc salt of 1-hydroxy-2-pyridinethione
US4004030A (en) * 1972-07-11 1977-01-18 Th. Goldschmidt Ag Microbiocidally effective amines or amine mixtures
DE4201038C2 (en) * 1992-01-17 1996-03-28 Schuelke & Mayr Gmbh Disinfectant concentrate and amine and alcohol based disinfectants and their use
EP2596702B1 (en) * 2011-11-25 2015-05-27 Omya International AG Process for stabilizing bacterial content of aqueous ground natural calcium carbonate and/or precipitated calcium carbonate and/or dolomite and/or surface-reacted calcium carbonate-comprising mineral preparations

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2246524A (en) * 1938-08-10 1941-06-24 Monsanto Chemicals Germicide
US2250480A (en) * 1939-03-18 1941-07-29 Burton T Bush Inc Dihydroxy hexachloro diphenyl methane and method of producing the same
US2244712A (en) * 1939-12-04 1941-06-10 Monsanto Chemicals Control of ambrosia beetles

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3717579A (en) * 1970-10-05 1973-02-20 Goldschmidt Ag Th Biocidal preparation
WO1984000006A1 (en) * 1982-06-18 1984-01-05 Bucuresti Medicamente Anti-tumour pharmaceutical preparation

Also Published As

Publication number Publication date
DE1492383A1 (en) 1970-03-05
NL257911A (en)
NL133648C (en)
CH409250A (en) 1966-03-15
US3108036A (en) 1963-10-22
SE313891B (en) 1969-08-25

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