JPH0466470B2 - - Google Patents

Info

Publication number: JPH0466470B2
Authority: JP; Japan
Prior art keywords: formula; general formula; reaction; dialkylethylenediamine; compound
Prior art date: 1986-07-18
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

JP61167872A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6327466A (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.)

1986-07-18

Filing date

1986-07-18

Publication date

1992-10-23

1986-07-18 Application filed by Nippon Shokubai Co Ltd filed Critical Nippon Shokubai Co Ltd

1986-07-18 Priority to JP61167872A priority Critical patent/JPS6327466A/ja

1988-02-05 Publication of JPS6327466A publication Critical patent/JPS6327466A/ja

1992-10-23 Publication of JPH0466470B2 publication Critical patent/JPH0466470B2/ja

Status Granted legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 claims description 19
235000014113 dietary fatty acids Nutrition 0.000 claims description 14
229930195729 fatty acid Natural products 0.000 claims description 14
239000000194 fatty acid Substances 0.000 claims description 14
150000004665 fatty acids Chemical class 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 12
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 description 11
230000018044 dehydration Effects 0.000 description 9
238000006297 dehydration reaction Methods 0.000 description 9
238000000034 method Methods 0.000 description 9
238000000862 absorption spectrum Methods 0.000 description 8
238000007112 amidation reaction Methods 0.000 description 8
239000007795 chemical reaction product Substances 0.000 description 8
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
238000000921 elemental analysis Methods 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
HLTMVWQXGLNLCU-UHFFFAOYSA-N n'-[2-(dimethylamino)ethyl]ethane-1,2-diamine Chemical compound CN(C)CCNCCN HLTMVWQXGLNLCU-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
229910001873 dinitrogen Inorganic materials 0.000 description 5
-1 polyethylene Polymers 0.000 description 5
150000003839 salts Chemical group 0.000 description 5
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 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
239000002280 amphoteric surfactant Chemical group 0.000 description 3
239000002216 antistatic 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
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 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
239000000080 wetting agent Substances 0.000 description 3
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
CJKRXEBLWJVYJD-UHFFFAOYSA-N N,N'-diethylethylenediamine Chemical compound CCNCCNCC CJKRXEBLWJVYJD-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 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
230000015572 biosynthetic process Effects 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
239000012459 cleaning agent Substances 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
238000004821 distillation Methods 0.000 description 2
229960003750 ethyl chloride Drugs 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
239000000155 melt Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920000768 polyamine Polymers 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
238000005956 quaternization reaction Methods 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
LHORZPMPPHTXFQ-UHFFFAOYSA-N 1-chloroethanesulfonic acid Chemical compound CC(Cl)S(O)(=O)=O LHORZPMPPHTXFQ-UHFFFAOYSA-N 0.000 description 1
LBFFKXDGKVMZQS-UHFFFAOYSA-N 2-(3-aminopropylamino)ethane-1,1-diol Chemical compound NCCCNCC(O)O LBFFKXDGKVMZQS-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
239000003599 detergent Substances 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002462 imidazolines Chemical class 0.000 description 1
KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Detergent Compositions (AREA)

JP61167872A 1986-07-18 1986-07-18 新規なｎ−アルキルアミドエチル−ｎ”，ｎ”−ジアルキルエチレンジアミン化合物およびその製造方法 Granted JPS6327466A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP61167872A JPS6327466A (ja)	1986-07-18	1986-07-18	新規なｎ−アルキルアミドエチル−ｎ”，ｎ”−ジアルキルエチレンジアミン化合物およびその製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP61167872A JPS6327466A (ja)	1986-07-18	1986-07-18	新規なｎ−アルキルアミドエチル−ｎ”，ｎ”−ジアルキルエチレンジアミン化合物およびその製造方法

Publications (2)

Publication Number	Publication Date
JPS6327466A JPS6327466A (ja)	1988-02-05
JPH0466470B2 true JPH0466470B2 (pl)	1992-10-23

Family

ID=15857644

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61167872A Granted JPS6327466A (ja)	1986-07-18	1986-07-18	新規なｎ−アルキルアミドエチル−ｎ”，ｎ”−ジアルキルエチレンジアミン化合物およびその製造方法

Country Status (1)

Country	Link
JP (1)	JPS6327466A (pl)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10015081C1 (de) *	2000-03-28	2001-11-08	Roland Diehm	Thermometerflüssigkeit

1986
- 1986-07-18 JP JP61167872A patent/JPS6327466A/ja active Granted

Also Published As

Publication number	Publication date
JPS6327466A (ja)	1988-02-05

Publication	Publication Date	Title
JP3004466B2 (ja)	2000-01-31	１回および２回置換されたマロン酸のモノエステル−モノアミド、モノ酸−モノアミドおよびビス−アミドの製造法、ならびにこの方法で製造された化合物
EP0486510B1 (en)	1996-02-14	Cyclic amidocarboxy surfactants, synthesis and use thereof
CN1127158A (zh)	1996-07-24	有多个疏水和亲水基团的阴离子型表面活性剂
JPH069516A (ja)	1994-01-18	水性ベタイン溶液の製造方法
AU652982B2 (en)	1994-09-15	Process for the preparation of fluoroaliphatic aminocarboxylate surfactants
US5470992A (en)	1995-11-28	Method for the synthesis of betaines containing≦10 ppm of organically bound chlorine
EP0746541A1 (en)	1996-12-11	Taurine derivatives for use in cleanser compositions
US5464565A (en)	1995-11-07	Process for the preparation of highly concentrated free-flowing aqueous solutions of betaines
JPH0466470B2 (pl)	1992-10-23
JPS6338343B2 (pl)	1988-07-29
JPH0476988B2 (pl)	1992-12-07
JPS61106544A (ja)	1986-05-24	第四級アンモニウム塩の製造法
JP3357414B2 (ja)	2002-12-16	増泡剤
JP4092739B2 (ja)	2008-05-28	アゾエステル化合物の新規な製造方法
KR102844817B1 (ko)	2025-08-11	S- 및 o-디아실화된 감마-글루타밀-시스테아민 전구약물의 생산 방법
US3534094A (en)	1970-10-13	Production of alpha,omega-diaminoalkane carboxylic acids
JP3067852B2 (ja)	2000-07-24	アミドアミン及びその製造法
JPH03271265A (ja)	1991-12-03	新規アスパラギン酸誘導体及びその製造方法並びにその製造中間体
JP2698601B2 (ja)	1998-01-19	両性界面活性剤組成物の製造方法
JP3563474B2 (ja)	2004-09-08	新規な第４級アンモニウム塩及びその製造法
JPH01268667A (ja)	1989-10-26	界面活性剤の製造方法
KR940011527B1 (ko)	1994-12-20	디알킬 프로판디이미데이트 디하이드로할라이드의 개량된 제조방법
JPS6139939B2 (pl)	1986-09-06
SU727634A1 (ru)	1980-04-15	Способ получени -(2-аза-2-нитроалкил)-амидов
JPH05294909A (ja)	1993-11-09	アシルイミノ二塩基酸の製造法