JPH0131761B2 - - Google Patents
Info
- Publication number
- JPH0131761B2 JPH0131761B2 JP59154436A JP15443684A JPH0131761B2 JP H0131761 B2 JPH0131761 B2 JP H0131761B2 JP 59154436 A JP59154436 A JP 59154436A JP 15443684 A JP15443684 A JP 15443684A JP H0131761 B2 JPH0131761 B2 JP H0131761B2
- Authority
- JP
- Japan
- Prior art keywords
- chitin
- cationized
- cosmetics
- water
- formula
- 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
- 229920002101 Chitin Polymers 0.000 claims description 55
- 239000002253 acid Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000002537 cosmetic Substances 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000001179 sorption measurement Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920001661 Chitosan Polymers 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000003842 bromide salts Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- -1 for example Chemical compound 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 150000004694 iodide salts Chemical class 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000013076 target substance Substances 0.000 description 2
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 description 2
- HPLFXTUAVXJDPJ-UHFFFAOYSA-M (3-chloro-2-hydroxypropyl)-triethylazanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC(O)CCl HPLFXTUAVXJDPJ-UHFFFAOYSA-M 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- OVRNDRQMDRJTHS-UHFFFAOYSA-N N-acelyl-D-glucosamine Natural products CC(=O)NC1C(O)OC(CO)C(O)C1O OVRNDRQMDRJTHS-UHFFFAOYSA-N 0.000 description 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical group 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- WQGFIYIFPAXLPK-UHFFFAOYSA-M ethyl-dimethyl-(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].CC[N+](C)(C)CC1CO1 WQGFIYIFPAXLPK-UHFFFAOYSA-M 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229950006780 n-acetylglucosamine Drugs 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- QVOJVKONBAJKMA-UHFFFAOYSA-M triethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1CO1 QVOJVKONBAJKMA-UHFFFAOYSA-M 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15443684A JPS6134004A (ja) | 1984-07-25 | 1984-07-25 | 新規カチオン化キチンの製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15443684A JPS6134004A (ja) | 1984-07-25 | 1984-07-25 | 新規カチオン化キチンの製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6134004A JPS6134004A (ja) | 1986-02-18 |
| JPH0131761B2 true JPH0131761B2 (ko) | 1989-06-28 |
Family
ID=15584147
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15443684A Granted JPS6134004A (ja) | 1984-07-25 | 1984-07-25 | 新規カチオン化キチンの製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6134004A (ko) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3501891A1 (de) * | 1985-01-22 | 1986-07-24 | Wella Ag, 6100 Darmstadt | Kosmetische mittel auf der basis von quaternaeren chitosanderivaten, neue quaternaere hydroxypropyl-substituierte chitosanderivate sowie verfahren zu ihrer herstellung |
| DE3502833A1 (de) * | 1985-01-29 | 1986-07-31 | Wella Ag, 6100 Darmstadt | Kosmetische mittel auf der basis von quaternaeren chitosanderivaten, neue quaternaere hydroxyethyl-substituierte chitosanderivate sowie verfahren zu ihrer herstellung |
| US4946870A (en) * | 1986-06-06 | 1990-08-07 | Union Carbide Chemicals And Plastics Company Inc. | Delivery systems for pharmaceutical or therapeutic actives |
| DE3644097A1 (de) * | 1986-12-23 | 1988-07-07 | Wella Ag | Kosmetisches mittel auf der basis von chitosan und ampholytischen copolymerisaten sowie ein neues chitosan/polyampholyt-salz |
| JPS6456611A (en) * | 1987-08-25 | 1989-03-03 | Hoou Kk | Hair dye composition |
| DE19545325B4 (de) * | 1995-12-05 | 2005-03-03 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Herstellung von Chitosanalkylderivaten |
| US6482969B1 (en) | 2001-10-24 | 2002-11-19 | Dow Corning Corporation | Silicon based quaternary ammonium functional compositions and methods for making them |
| CN104017106B (zh) * | 2013-12-20 | 2016-03-23 | 湖州市中心医院 | 一种三甲铵基羟丙基甲壳素、中间体及其研制方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6431761A (en) * | 1987-07-27 | 1989-02-02 | Kissei Pharmaceutical | Polyhalogenoindoline derivative |
-
1984
- 1984-07-25 JP JP15443684A patent/JPS6134004A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6134004A (ja) | 1986-02-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4220513B2 (ja) | カチオン化ヒアルロン酸 | |
| JP5366816B2 (ja) | グリオキサール化カチオン性グアーの調製手順 | |
| KR20130084222A (ko) | 신규한 고점도 카복시메틸 셀룰로스 및 제조방법 | |
| JPS5942681B2 (ja) | カチオン変性セルロ−ス誘導体の製造方法 | |
| JPH0131761B2 (ko) | ||
| JPS6042761B2 (ja) | 化粧品基材 | |
| JPH11315102A (ja) | 両性グア―ガム誘導体の製造方法 | |
| JPH0649725B2 (ja) | カチオン性キトサン誘導体の製造方法 | |
| JPS6334161B2 (ko) | ||
| JP4310967B2 (ja) | 多糖類複合体の製造方法 | |
| JP3731007B2 (ja) | Ｎ−カルボキシアシルキトサン及びその製造方法 | |
| JP2693795B2 (ja) | 皮膚洗浄料 | |
| JP4395573B2 (ja) | 酸化キトサン化合物 | |
| JPH0649726B2 (ja) | アニオン性キトサン誘導体の製造方法 | |
| JPS6011921B2 (ja) | カチオン変性デンプン誘導体の製造方法 | |
| KR100381387B1 (ko) | 키토산유도체의제조방법 | |
| JP2826899B2 (ja) | キトサン誘導体、その製造方法及びそれよりなる洗剤用ビルダー及び保湿剤 | |
| JPH0570501A (ja) | カチオン性セルロース誘導体の製造方法 | |
| JP2687141B2 (ja) | 新規なキトサン化合物、該化合物の製造方法および該化合物を含む保湿剤 | |
| JPH0772201B2 (ja) | カチオン性ヒドロキシアルキルセルロ−スの製造法 | |
| JP2529729B2 (ja) | キトサン誘導体の製造法 | |
| JP2511675B2 (ja) | ポリオキシエチレン化キチンの製造方法 | |
| CN114292340B (zh) | 一种制备聚季铵盐-10的方法 | |
| JPS5930161B2 (ja) | カチオン化デキストラン誘導体、その製法ならびに利用 | |
| JPH02105801A (ja) | 新規なキトサン化合物、該化合物の製造方法および保湿剤としての用途 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |