GB1504390A - Alkoxylated n-alkyl derivatives of propylenediamine - Google Patents
Alkoxylated n-alkyl derivatives of propylenediamineInfo
- Publication number
- GB1504390A GB1504390A GB4968875A GB4968875A GB1504390A GB 1504390 A GB1504390 A GB 1504390A GB 4968875 A GB4968875 A GB 4968875A GB 4968875 A GB4968875 A GB 4968875A GB 1504390 A GB1504390 A GB 1504390A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- chr
- radical
- compound
- hydrogen
- 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
- 150000001875 compounds Chemical class 0.000 abstract 6
- -1 alkyl radical Chemical class 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000003641 microbiacidal effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
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
- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Abstract
1504390 Alkoxylated N-alkyl derivatives of propylenediamine TH GOLDSCHMIDT AG 3 Dec 1975 [4 Dec 1974] 49688/75 Heading C2C The invention comprises compounds of the general Formula I wherein R<SP>1</SP> is a cyclohexyl radical, R<SP>3</SP> is a straight-chain alkyl radical with 12 to 16 carbon atoms as hereinafter defined, each R<SP>2</SP>, which may be the same or different, is hydrogen or a CH 2 CHR<SP>4</SP>OH group, where R<SP>4</SP> is hydrogen or a methyl radical, at least one R<SP>2</SP> radical being a CH 2 CHR<SP>4</SP>OH group. By straight-chain alkyl radical with 12 to 16 carbon atoms is meant to include a mixture of alkyl radicals of different chain length which on average contain 12 to 16 carbon atoms. Also included within the scope of the invention are mixtures of a compound according to Formula I wherein one R<SP>2</SP> is CH 2 CHR<SP>4</SP>OH and wherein both R<SP>2</SP> are CH 2 CHR<SP>4</SP>OH. The compounds of Formula I or a mixture thereof when R<SP>2</SP> are different may be prepared by reacting ethylene oxide and/or propylene oxide with a diaminopropane compound of formula R<SP>1</SP>NH(CH 2 ) 3 NHR<SP>3</SP> wherein R<SP>1</SP> and R<SP>3</SP> are as defined above, reaction with ethylene oxide producing a compound wherein R 4 is hydrogen and reaction with propylene oxide producing a compound wherein R 4 is methyl. The compounds of Formula I are used in microbicidal preparations which are described and claimed.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742457257 DE2457257C3 (en) | 1974-12-04 | Hydroxyethyl or -propyl derivatives of N-cyclohexyl-N'-alkyl-propylenediamine and microbicidal preparations based on them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1504390A true GB1504390A (en) | 1978-03-22 |
Family
ID=5932450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4968875A Expired GB1504390A (en) | 1974-12-04 | 1975-12-03 | Alkoxylated n-alkyl derivatives of propylenediamine |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE836285A (en) |
| FR (1) | FR2293418A1 (en) |
| GB (1) | GB1504390A (en) |
| IT (1) | IT1052432B (en) |
| NL (1) | NL7513889A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997001360A2 (en) * | 1995-06-26 | 1997-01-16 | Concat, Ltd. | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
-
1975
- 1975-11-27 NL NL7513889A patent/NL7513889A/en not_active Application Discontinuation
- 1975-11-27 IT IT5243475A patent/IT1052432B/en active
- 1975-11-28 FR FR7536450A patent/FR2293418A1/en not_active Withdrawn
- 1975-12-03 GB GB4968875A patent/GB1504390A/en not_active Expired
- 1975-12-04 BE BE162457A patent/BE836285A/en unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997001360A2 (en) * | 1995-06-26 | 1997-01-16 | Concat, Ltd. | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
| WO1997001360A3 (en) * | 1995-06-26 | 1997-03-13 | Concat Ltd | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
| US5874573A (en) * | 1995-06-26 | 1999-02-23 | Concat, Inc. | Compounds with chelation affinity and selectivity for first transition series elements: use in medical therapy |
| US6583182B1 (en) | 1995-06-26 | 2003-06-24 | Chelator Llc | Compounds with chelation affinity and selectivity for first transition series elements: use in medical therapy and diagnosis |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2293418A1 (en) | 1976-07-02 |
| BE836285A (en) | 1976-04-01 |
| DE2457257A1 (en) | 1976-06-10 |
| DE2457257B2 (en) | 1977-02-10 |
| IT1052432B (en) | 1981-06-20 |
| NL7513889A (en) | 1976-06-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1164825A (en) | New N-Substituted Nitro-Anilines | |
| ES470159A1 (en) | Components of catalysts for polymerizing alpha-olefins and the catalysts formed from the components | |
| GB1445503A (en) | Acylamino acid amides | |
| GB1413783A (en) | Alkylaryloxyphosphazene polymers | |
| GB1497557A (en) | Phosphorus and sulphur-containing amides and thioamides | |
| MY109628A (en) | An improved proces for the preparation of substituted indoline derivatives | |
| GB1024484A (en) | Improvements in and relating to rubber compositions | |
| ES8506745A1 (en) | Novel organic platinum complex and process for the preparation thereof. | |
| ATE50773T1 (en) | ALKYLRESORCINOPHOSPHITES. | |
| GB1504390A (en) | Alkoxylated n-alkyl derivatives of propylenediamine | |
| GB1511177A (en) | Alkali-stable polyoxyethylene acetal surfactants | |
| KR880003945A (en) | Novel compounds and preparations thereof, and pharmaceutical compositions thereof | |
| CA1273946C (en) | Anticonvulsant gamma-thiobutyrolactone derivatives | |
| GB1270784A (en) | Processes for carrying out chemical reactions initiated by free-radicals using 1,2-diaryl-1,2-dicyano-ethane compounds as radical initiators | |
| GB1507414A (en) | Hydantoin derivatives | |
| MY100938A (en) | Arylkylimidazole derivatives. | |
| GB1483866A (en) | Gasoline compositions | |
| GB1430926A (en) | 2-amino-3,4-dihydropyridines their production and their medicinal use | |
| ES8609184A1 (en) | Agent for the fluoridation of organic compounds particularly acetylenic compounds, preparation process thereof and utilization thereof in nucleophilic substitution or addition reactions. | |
| ES8305377A1 (en) | Nitrosourea derivatives, a process for preparing same and therapeutic compositions. | |
| GB1423017A (en) | Phosphorothionoamidate derivatives having plant growth regulating properties | |
| GB1237658A (en) | Substituted 1-oxy-1-thiono-3-halogen- or -3-alkyl phospholines | |
| GB1345645A (en) | Diamido amino sulphonates and preparation thereof | |
| GB1129240A (en) | Improvements in or relating to antibiotic derivatives and the manufacture thereof | |
| KR910016673A (en) | Method for preparing hydroxyphenyl propionate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |