CH400179A - Verfahren zur Herstellung von Triamin-Säureadditionssalzen - Google Patents

Verfahren zur Herstellung von Triamin-Säureadditionssalzen

Info

Publication number: CH400179A
Authority: CH; Switzerland
Prior art keywords: bis; ethylhexyl; propanetriamine; methyl; dimethyl
Prior art date: 1960-09-19

Application number

CH1091561A

Other languages

German (de)

English (en)

Inventor

G Mulinos Michael

Original Assignee

Commercial Solvents Corp

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.)

1960-09-19

Filing date

1961-09-19

Publication date

1965-10-15

1961-09-19 Application filed by Commercial Solvents Corp filed Critical Commercial Solvents Corp

1965-10-15 Publication of CH400179A publication Critical patent/CH400179A/de

Links

239000002253 acid Substances 0.000 title claims description 10
238000000034 method Methods 0.000 title claims description 8
150000003839 salts Chemical class 0.000 title claims description 8
238000002360 preparation method Methods 0.000 title claims description 4
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 19
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 16
FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims description 13
KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 claims description 11
229960002703 undecylenic acid Drugs 0.000 claims description 11
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
239000000203 mixture Substances 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
-1 N1,2-dimethyl-N1, N3-bis- (2-ethylhexyl) 1,2,3-propanetriamine mono-propionate Chemical compound 0.000 description 54
RCNXUTDLDYQBIV-UHFFFAOYSA-N 1-n,3-n-bis(2-ethylhexyl)-3-n,2-dimethylpropane-1,2,3-triamine Chemical compound CCCCC(CC)CNCC(C)(N)CN(C)CC(CC)CCCC RCNXUTDLDYQBIV-UHFFFAOYSA-N 0.000 description 8
235000019260 propionic acid Nutrition 0.000 description 7
239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 6
229960002446 octanoic acid Drugs 0.000 description 6
239000000126 substance Substances 0.000 description 6
230000000855 fungicidal effect Effects 0.000 description 5
239000002674 ointment Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
STNVDPRWLDHKCY-UHFFFAOYSA-N 1-n,3-n-bis(2-ethylhexyl)-2-methylpropane-1,2,3-triamine Chemical compound CCCCC(CC)CNCC(C)(N)CNCC(CC)CCCC STNVDPRWLDHKCY-UHFFFAOYSA-N 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
206010017533 Fungal infection Diseases 0.000 description 2
208000031888 Mycoses Diseases 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000003599 detergent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000007858 starting material Substances 0.000 description 2
230000001225 therapeutic effect Effects 0.000 description 2
229940075466 undecylenate Drugs 0.000 description 2
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
241000228212 Aspergillus Species 0.000 description 1
241000222120 Candida <Saccharomycetales> Species 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
241000228143 Penicillium Species 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
239000000686 essence Substances 0.000 description 1
230000004313 glare Effects 0.000 description 1
239000008311 hydrophilic ointment Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000007794 irritation Effects 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 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
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/122—Propionic acid
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/126—Acids containing more than four carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CH1091561A 1960-09-19 1961-09-19 Verfahren zur Herstellung von Triamin-Säureadditionssalzen CH400179A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US56661A US3164619A (en)	1960-09-19	1960-09-19	Triamine acid addition salts of caprylic, propionic and undecylenic acids

Publications (1)

Publication Number	Publication Date
CH400179A true CH400179A (de)	1965-10-15

Family

ID=22005851

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1091561A CH400179A (de)	1960-09-19	1961-09-19	Verfahren zur Herstellung von Triamin-Säureadditionssalzen

Country Status (5)

Country	Link
US (1)	US3164619A (fr)
BE (1)	BE608307A (fr)
CH (1)	CH400179A (fr)
FR (1)	FR1530M (fr)
GB (1)	GB930440A (fr)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2290174A (en) *	1940-10-04	1942-07-21	Albert K Epstein	Bactericidal, germicidal, and antiseptic materials
US2436779A (en) *	1944-12-08	1948-02-24	Commercial Solvents Corp	Triamino propanes
US2994765A (en) *	1957-08-09	1961-08-01	Eugene C Adam	Emergency vehicle alarm device
US2998438A (en) *	1958-03-31	1961-08-29	Merck & Co Inc	Eulicin and process for production

1960
- 1960-09-19 US US56661A patent/US3164619A/en not_active Expired - Lifetime
1961
- 1961-09-18 FR FR873465A patent/FR1530M/fr active Active
- 1961-09-19 BE BE608307A patent/BE608307A/fr unknown
- 1961-09-19 CH CH1091561A patent/CH400179A/de unknown
- 1961-09-19 GB GB33590/61A patent/GB930440A/en not_active Expired

Also Published As

Publication number	Publication date
BE608307A (fr)	1962-01-15
US3164619A (en)	1965-01-05
FR1530M (fr)	1962-10-15
GB930440A (en)	1963-07-03

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