GB963907A - Compositions including a phenolic component and a polyamine component - Google Patents
Compositions including a phenolic component and a polyamine componentInfo
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, 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
- A01N37/18—Biocides, 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
- A01N37/20—Biocides, 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.
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)
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)
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)
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 |
-
0
- NL NL133648D patent/NL133648C/xx active
- NL NL257911D patent/NL257911A/xx unknown
-
1959
- 1959-11-12 US US852172A patent/US3108036A/en not_active Expired - Lifetime
-
1960
- 1960-11-10 GB GB38631/60A patent/GB963907A/en not_active Expired
- 1960-11-11 SE SE10856/60A patent/SE313891B/xx unknown
- 1960-11-14 CH CH1270960A patent/CH409250A/en unknown
Cited By (2)
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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