JPH0476988B2 - - Google Patents

Info

Publication number: JPH0476988B2
Authority: JP; Japan
Prior art keywords: formula; general formula; alkylimidazoline; dialkylaminoethyl; reaction
Prior art date: 1986-07-17
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

JP61166668A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6327480A (ja

Inventor

Seiichi Suzuki

Kotaro Nakagawa

Yutaka Morimoto

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.)

Nippon Shokubai Co Ltd

Original Assignee

Nippon Shokubai Co Ltd

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.)

1986-07-17

Filing date

1986-07-17

Publication date

1992-12-07

1986-07-17 Application filed by Nippon Shokubai Co Ltd filed Critical Nippon Shokubai Co Ltd

1986-07-17 Priority to JP61166668A priority Critical patent/JPS6327480A/ja

1988-02-05 Publication of JPS6327480A publication Critical patent/JPS6327480A/ja

1992-12-07 Publication of JPH0476988B2 publication Critical patent/JPH0476988B2/ja

Status Granted legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 11
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
235000014113 dietary fatty acids Nutrition 0.000 claims description 7
229930195729 fatty acid Natural products 0.000 claims description 7
239000000194 fatty acid Substances 0.000 claims description 7
150000004665 fatty acids Chemical class 0.000 claims description 7
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
-1 alkyl imidazoline compound Chemical class 0.000 description 12
238000000862 absorption spectrum Methods 0.000 description 10
238000000034 method Methods 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
239000007795 chemical reaction product Substances 0.000 description 8
230000018044 dehydration Effects 0.000 description 8
238000006297 dehydration reaction Methods 0.000 description 8
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
238000002329 infrared spectrum Methods 0.000 description 6
CEFDTSBDWYXVHY-UHFFFAOYSA-N n'-[2-(diethylamino)ethyl]ethane-1,2-diamine Chemical compound CCN(CC)CCNCCN CEFDTSBDWYXVHY-UHFFFAOYSA-N 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
HLTMVWQXGLNLCU-UHFFFAOYSA-N n'-[2-(dimethylamino)ethyl]ethane-1,2-diamine Chemical compound CN(C)CCNCCN HLTMVWQXGLNLCU-UHFFFAOYSA-N 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000002253 acid Substances 0.000 description 4
238000007112 amidation reaction Methods 0.000 description 4
229910001873 dinitrogen Inorganic materials 0.000 description 4
238000000921 elemental analysis Methods 0.000 description 4
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
238000005259 measurement Methods 0.000 description 4
YPHVKORVIPKRBT-UHFFFAOYSA-N n,n-diethyl-2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanamine Chemical compound CCCCCCCCCCCC1=NCCN1CCN(CC)CC YPHVKORVIPKRBT-UHFFFAOYSA-N 0.000 description 4
238000007363 ring formation reaction Methods 0.000 description 4
150000003839 salts Chemical group 0.000 description 4
238000003756 stirring Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
239000005639 Lauric acid Substances 0.000 description 3
235000021355 Stearic acid Nutrition 0.000 description 3
239000002216 antistatic agent Substances 0.000 description 3
239000012459 cleaning agent Substances 0.000 description 3
239000002537 cosmetic Substances 0.000 description 3
239000000645 desinfectant Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000004088 foaming agent Substances 0.000 description 3
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
239000008117 stearic acid Substances 0.000 description 3
LHORZPMPPHTXFQ-UHFFFAOYSA-N 1-chloroethanesulfonic acid Chemical compound CC(Cl)S(O)(=O)=O LHORZPMPPHTXFQ-UHFFFAOYSA-N 0.000 description 2
QEGKXSHUKXMDRW-UHFFFAOYSA-N 2-chlorosuccinic acid Chemical compound OC(=O)CC(Cl)C(O)=O QEGKXSHUKXMDRW-UHFFFAOYSA-N 0.000 description 2
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
239000002280 amphoteric surfactant Chemical group 0.000 description 2
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
229940073608 benzyl chloride Drugs 0.000 description 2
229960003237 betaine Drugs 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 2
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
238000010586 diagram Methods 0.000 description 2
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
229960003750 ethyl chloride Drugs 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
125000002636 imidazolinyl group Chemical group 0.000 description 2
HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 2
LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003906 humectant Substances 0.000 description 1
239000000203 mixture Substances 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000005956 quaternization reaction Methods 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Dermatology (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Detergent Compositions (AREA)

JP61166668A 1986-07-17 1986-07-17 新規な１−（ｎ，ｎ−ジアルキルアミノエチル）−２−アルキルイミダゾリン化合物およびその製法 Granted JPS6327480A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP61166668A JPS6327480A (ja)	1986-07-17	1986-07-17	新規な１−（ｎ，ｎ−ジアルキルアミノエチル）−２−アルキルイミダゾリン化合物およびその製法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP61166668A JPS6327480A (ja)	1986-07-17	1986-07-17	新規な１−（ｎ，ｎ−ジアルキルアミノエチル）−２−アルキルイミダゾリン化合物およびその製法

Publications (2)

Publication Number	Publication Date
JPS6327480A JPS6327480A (ja)	1988-02-05
JPH0476988B2 true JPH0476988B2 (pl)	1992-12-07

Family

ID=15835512

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61166668A Granted JPS6327480A (ja)	1986-07-17	1986-07-17	新規な１−（ｎ，ｎ−ジアルキルアミノエチル）−２−アルキルイミダゾリン化合物およびその製法

Country Status (1)

Country	Link
JP (1)	JPS6327480A (pl)

1986
- 1986-07-17 JP JP61166668A patent/JPS6327480A/ja active Granted

Also Published As

Publication number	Publication date
JPS6327480A (ja)	1988-02-05

Publication	Publication Date	Title
US5292942A (en)	1994-03-08	Process for the preparation of aqueous betaine solutions
ES8101040A1 (es)	1980-12-16	Procedimiento para la preparacion de betainas
JPH0867658A (ja)	1996-03-12	第四級ジエステルの調製方法
DE3216722A1 (de)	1983-11-10	4-halomethylbenzoesaeure-alkylester-imine und verfahren zu deren herstellung
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US4269730A (en)	1981-05-26	Substituted imidazoline reactions with chloroacetate salts
JPH0476988B2 (pl)	1992-12-07
JP4357656B2 (ja)	2009-11-04	第４級アンモニウム塩
US2781376A (en)	1957-02-12	Detergent sulphonic acid and sulphate salts of certain amphoteric detergents
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JPH0468303B2 (pl)	1992-11-02
US2090595A (en)	1937-08-17	Process of preparing amido derivatives
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