序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
101 Alkyl sulfate/alkyl ether sulfate mixture and use JP18444888 1988-07-22 JPS6447756A 1989-02-22 UBUE PUROOKU; BUORUFUGANGU HOOHOSHIYOON
102 Sulfurized hydroxy ether, manufacture and use JP17796388 1988-07-15 JPS6438056A 1989-02-08 GIRUBERUTO SHIENKAA; ROBERUTO PIOORU; ZABIINE RIYUTSUTOUGE
103 Manufacture of sulfate betaine JP6067088 1988-03-16 JPS63243065A 1988-10-07 GERORUDO BURAUN; CHIYUNNII CHIYAN; KURISUTOSU FUAMUFUAKARISU; KURAUSU GURAAZERU
104 JPS6314707B2 - JP9542481 1981-06-22 JPS6314707B2 1988-04-01 KAARU JOOJI KURESUPAN
105 Continuous sulfation method JP18045984 1984-08-31 JPS6160643A 1986-03-28 HIRAKOUCHI YOSHIE; TAKAHASHI MASATOSHI
PURPOSE: To carry out the continuous sulfation, and to obtain high-quality sulfated product in an industrial scale, suppressing the side reactions, by forming a fluid thin film of an organic compound by a high-speed gas stream formed along the wall surface, and contacting the film of the organic compound with chlorosulfonic acid. CONSTITUTION: A high-speed gas stream flowing downward is formed along the inner wall of te reaction tube 11 from the high-speed gas inlet 17. A liquid organic compound (e.g. 8W20C straight or branched-chain alcohol) is supplied from te raw material inlet 19 along the inner wall, and is formed to a circular thin liquid film by the high-speed gas stream. Chlorosulfonic acid is introduced through the inlet 31, and sprayed by the inert gas, etc. introduced from the gas inlet 33. The sprayed chlorosulfonic acid is contacted with the organic compound to effect the continuous sulfation of the compound. Since the organic compound is reacted in the formula thin film, the heat-exchange efficiency is high, and since the chlorosulfonic acid is contacted and absorbed in the form of fine particles, it can be added uniformly to the organic compound, and a sulfated product containing little unreacted organic compound and by-product can be produced. COPYRIGHT: (C)1986,JPO&Japio
106 Sulfurization of compound containing hydroxyethyl group JP18380785 1985-08-21 JPS6157546A 1986-03-24 HANSURUDORUFU SHIYUBUANDAA
107 JPS6012347B2 - JP5161275 1975-04-30 JPS6012347B2 1985-04-01 RAASUROO FUOIAA; AARUPAADO FURUKA; FUERENTSU SHEBESHUTEIEEN; YOORAN HERUCHERU; ERUJEEBETO BENDEIFUI
1504541 Compositions containing amino acid derivatives CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT 28 April 1975 [29 April 1974 26 March 1975] 17608/75 Heading A5B [Also in Divisions C2 and C3] Cosmetic and pharmaceutical compositions contain (I) and/or salts thereof as active ingredient wherein A<SP>1</SP> stands for hydroxy, C 1-4 alkoxy, cycloalkoxy, aralkoxy, substituted aralkoxy, aryloxy, substituted aryloxy or a group of the general formulae: wherein R<SP>14</SP> is hydrogen, C 1-4 alkyl or aralkyl, R<SP>6</SP> is hydrogen, C 1-5 alkyl, aralkyl, hydroxysubstituted aralkyl, heteroaralkyl or a group of the general formula: Y is hydroxy, amino, alkylamino, dialkylamino, C 1-4 alkoxy or aralkoxy, and r is an integer of from 1 to 10 or an average polymerization grade of up to 2000, B<SP>1</SP> is a group of the formulae -SO 2 OH, -OSO 2 OH, -O-PO(OH) 2 or -S-S-R<SP>11</SP>, wherein R<SP>11</SP> is C 1-4 alkyl, aralkyl or aryl or a residue obtained when removing group B<SP>1</SP> from the general formula (I), R stands for hydrogen, C 1-4 alkyl or aralkyl, R<SP>x</SP> stands for hydrogen or halogen, R<SP>1</SP> stands for hydrogen, C 1-4 alkyl, aryl, aryl having a nitro or alkoxy substituent, aralkyl, substituted aralkyl, alkoxycarbonyl, cycloalkoxycarbonyl, aralkoxycarbonyl, substituted aralkoxycarbonyl having, e.g. a halogen, alkoxy, nitro, phenylazo or alkoxyphenylazo substituent, unsubstituted or substituted aryloxycarbonyl, acyl, arylsulfonyl or group (wherein R<SP>6</SP> has the same meanings as defined above and p is an integer of from 1 to 10 or an average polymerization degree of up to 2000), R<SP>2</SP> stands for hydrogen, C 1-4 alkyl, or aralkyl or R<SP>2</SP> and R<SP>2</SP> may each stand for a -CO- group and form a ring through an o-phenylene, alkylene or -CH=CH- group, R<SP>3</SP> stands for hydrogen, carboxy or carbalkoxy, R<SP>4</SP> stands for hydrogen, halogen, C 1-4 alkyl or hydroxy, R<SP>5</SP> stands for hydrogen, halogen, C 1-4 alkyl, carboxy, carboxamido, carbalkoxy or carboaralkoxy, m is 1, 2 or 3, n is 1, 2, 3 or 4, s is 0, 1, 2, 3 or 4, and t is 1, 2 or 3.
108 JPS5951937B2 - JP6205877 1977-05-27 JPS5951937B2 1984-12-17 BAATON BURUTSUKUSU; RICHAADO JEI BURUTSUKUSU
109 JPS5943936B2 - JP14406677 1977-12-02 JPS5943936B2 1984-10-25 KAARU JOOJI KURESUPAN
110 Copolymer JP20472382 1982-11-24 JPS5891708A 1983-05-31 KAARU JIYOOJI KURESUPAN
111 Omega-fluorosulfato-perfluoro-(2-methyl- alkane-3-one) and manufacture of perfluoro- isopropylketocarboxylic acid fluoride derived therefrom JP14255381 1981-09-11 JPS5781455A 1982-05-21 HANSU MIRAUERU; GIYUNTERU JIIGEMUNTO; UERUNERU SHIYUUERUTOFUEGERU
112 Manufacture of polyfluorocarbonyl compounds and some novel compounds among these compounds JP14255281 1981-09-11 JPS5781434A 1982-05-21 HANSU MIRAUERU; GIYUNTERU JIIGEMUNTO; UERUNERU SHIYUUERUTOFUEGERU
113 Preparation of perfluorocarbonyl sulfonic acid fluoride JP14255581 1981-09-11 JPS5779186A 1982-05-18 HANSU MIRAUERU; UERUNERU SHIYUUERUTOFUEGERU
114 N-allenylalkyl-acetanilides, manufacture and fungicidal composition JP11236881 1981-07-20 JPS5756445A 1982-04-05 BUINFURIITO RUNKENHAIMAA; BUORUFUGANGU HIYUURAA; IERUKU SHIYUTETSUTAA; BUIRUHERUMU BURANDESU
115 JPS5715113B2 - JP11518277 1977-09-27 JPS5715113B2 1982-03-29
116 Biodegradable zwitterionic surfactant compound and detergent composition containing it JP854281 1981-01-22 JPS56150048A 1981-11-20 JIYOOJI EDOWAADO UENTORAA; JIYOSEFU MAKUGURADEII; YUUJIN POORU GOSERINKU; UIRIAMU AJIARON SHIRII
117 Natural resin acid surfactant compound and surfactant made therefrom JP11745279 1979-09-14 JPS5540690A 1980-03-22 URURITSUHI KUNTSUTSUE; HAINTSU UURITSUHI
118 JPS5417591B2 - JP11909076 1976-10-04 JPS5417591B2 1979-06-30
119 Purification of sulfuric ester slats of higher alcohols or ethylene oxide adducts thereof JP12905377 1977-10-26 JPS5463021A 1979-05-21 YOSHIDA SEIICHI; YAMASHITA NOBORU; YAMADA MINORU; YAMAGAMI MITSURU
PURPOSE: To obtain highly pure title compound quite easily, which is an anionic surface active agent. by purifying the crude compound in the presence of H 2O 2. CONSTITUTION: Highly pure sulfuric ester salt of a higher alcohol such as 12W13C oxo alcohol, or ehylene oxide adduct thereof, is obtained by purifying the crude compound in the presence of 0.001W1%, preferably 0.002W0.05%, based on the sulfuric ester salt of higher alcohol or the ethylene oxide adduct thereof, of H 2O 2, a peroxy acid or their salts, and reacting at 10W100°C for 20W180 min. EFFECT: IMproved stability against the use of perfumes or dyes. USE: Base of household detergents, shampoo, etc. COPYRIGHT: (C)1979,JPO&Japio
120 Preparation of alcohol sulfuric acid ester salt JP11518277 1977-09-27 JPS5452031A 1979-04-24 YAMAGUCHI HACHIROU
PURPOSE: To prepare an almost colorless title compound in high yield with little side ractions under mild conditions, by sulfating a primary or secondary alcohol having 6-18 C atoms using a complex of boric anhydride and sulfur trioxide as novel sulfating agent. CONSTITUTION: An alcohol sulfuric acid ester salt (e.g. cyclohexanol sulfuric acid ester ammonium salt) is prepared by sulfating a 6-18C primary or secondary alcohol (e.g. cyclohexanol) in a solvent pref. comprising dimethylformamide containing a chlorinated alkane such as 1,2-dichloroethane, at a low temperature (e.g. -20- -10°C) using a complex of boric anhydride and sulfur trioxide obtained by the reaction of boric anhydride with sulfur trioxide in a solvent, as sulfating agent COPYRIGHT: (C)1979,JPO&Japio
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