JPH05247061A - 透明で無色のアルコキシシランモノマーの調製方法 - Google Patents
透明で無色のアルコキシシランモノマーの調製方法Info
- Publication number
- JPH05247061A JPH05247061A JP4264414A JP26441492A JPH05247061A JP H05247061 A JPH05247061 A JP H05247061A JP 4264414 A JP4264414 A JP 4264414A JP 26441492 A JP26441492 A JP 26441492A JP H05247061 A JPH05247061 A JP H05247061A
- Authority
- JP
- Japan
- Prior art keywords
- product
- colorless
- ammonia
- group
- reaction
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000000178 monomer Substances 0.000 title claims abstract description 8
- 238000002360 preparation method Methods 0.000 title abstract description 3
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000003377 acid catalyst Substances 0.000 claims abstract description 18
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 6
- 150000007522 mineralic acids Chemical class 0.000 claims description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 150000001298 alcohols Chemical class 0.000 claims description 7
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 12
- 238000000746 purification Methods 0.000 abstract description 6
- 239000000047 product Substances 0.000 description 57
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 56
- 229910021529 ammonia Inorganic materials 0.000 description 28
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 238000006884 silylation reaction Methods 0.000 description 16
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 12
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 11
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- WGGNJZRNHUJNEM-UHFFFAOYSA-N 2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinane Chemical compound C[Si]1(C)N[Si](C)(C)N[Si](C)(C)N1 WGGNJZRNHUJNEM-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- -1 2,4,4-trimethylpentyl group Chemical group 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- JROMGTZTUZNJJY-UHFFFAOYSA-N 1,3,5-tris(ethenyl)-2,4,6-trimethyl-1,3,5,2,4,6-triazatrisilinane Chemical compound C(=C)N1[SiH](N([SiH](N([SiH]1C)C=C)C)C=C)C JROMGTZTUZNJJY-UHFFFAOYSA-N 0.000 description 1
- FIADVASZMLCQIF-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octamethyl-1,3,5,7,2,4,6,8-tetrazatetrasilocane Chemical compound C[Si]1(C)N[Si](C)(C)N[Si](C)(C)N[Si](C)(C)N1 FIADVASZMLCQIF-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- LQMOOYRQYFXGSQ-UHFFFAOYSA-N C1(=CC=CC2=CC=C3C=C4C=CC=CC4=CC3=C12)[SiH](N[SiH2]C)C Chemical compound C1(=CC=CC2=CC=C3C=C4C=CC=CC4=CC3=C12)[SiH](N[SiH2]C)C LQMOOYRQYFXGSQ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- VJFUNCKASZQOPO-UHFFFAOYSA-N N-dioctylsilyl-N-trimethylsilylmethanamine Chemical compound CCCCCCCC[SiH](N(C)[Si](C)(C)C)CCCCCCCC VJFUNCKASZQOPO-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- HIMXYMYMHUAZLW-UHFFFAOYSA-N [[[dimethyl(phenyl)silyl]amino]-dimethylsilyl]benzene Chemical compound C=1C=CC=CC=1[Si](C)(C)N[Si](C)(C)C1=CC=CC=C1 HIMXYMYMHUAZLW-UHFFFAOYSA-N 0.000 description 1
- WYUIWUCVZCRTRH-UHFFFAOYSA-N [[[ethenyl(dimethyl)silyl]amino]-dimethylsilyl]ethene Chemical compound C=C[Si](C)(C)N[Si](C)(C)C=C WYUIWUCVZCRTRH-UHFFFAOYSA-N 0.000 description 1
- QYJHBNLRANFWHO-UHFFFAOYSA-N [ethenyl-[(ethenyl-methyl-phenylsilyl)amino]-methylsilyl]benzene Chemical compound C=1C=CC=CC=1[Si](C)(C=C)N[Si](C)(C=C)C1=CC=CC=C1 QYJHBNLRANFWHO-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- VQKFNUFAXTZWDK-UHFFFAOYSA-N alpha-methylfuran Natural products CC1=CC=CO1 VQKFNUFAXTZWDK-UHFFFAOYSA-N 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- SXSNZRHGAMVNJE-UHFFFAOYSA-N chloro-[[[chloromethyl(dimethyl)silyl]amino]-dimethylsilyl]methane Chemical compound ClC[Si](C)(C)N[Si](C)(C)CCl SXSNZRHGAMVNJE-UHFFFAOYSA-N 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C07F7/1872—Preparation; Treatments not provided for in C07F7/20
- C07F7/188—Preparation; Treatments not provided for in C07F7/20 by reactions involving the formation of Si-O linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US770376 | 1991-10-03 | ||
| US07/770,376 US5157139A (en) | 1991-10-03 | 1991-10-03 | Inorganic acid catalysed silylation reactions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05247061A true JPH05247061A (ja) | 1993-09-24 |
Family
ID=25088341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4264414A Pending JPH05247061A (ja) | 1991-10-03 | 1992-10-02 | 透明で無色のアルコキシシランモノマーの調製方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5157139A (enExample) |
| EP (1) | EP0535947B1 (enExample) |
| JP (1) | JPH05247061A (enExample) |
| KR (1) | KR100242750B1 (enExample) |
| AU (1) | AU648200B2 (enExample) |
| CA (1) | CA2079542A1 (enExample) |
| DE (1) | DE69230989T2 (enExample) |
| TW (1) | TW238311B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023536863A (ja) * | 2020-07-31 | 2023-08-30 | エルジー・ケム・リミテッド | アルコキシシラン化合物の製造方法 |
| JP2023536864A (ja) * | 2020-07-31 | 2023-08-30 | エルジー・ケム・リミテッド | アルコキシシラン化合物の製造方法 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5707550A (en) * | 1993-04-06 | 1998-01-13 | Dow Corning Corporation | Foam boosting of hair shampoo compositions |
| US5326557A (en) * | 1993-04-06 | 1994-07-05 | Dow Corning Corporation | Moisturizing compositions containing organosilicon compounds |
| US6017546A (en) * | 1993-07-06 | 2000-01-25 | Dow Corning Corporation | Water-in-volatile silicone emulsion gel cosmetic |
| US5847179A (en) * | 1997-10-02 | 1998-12-08 | Pcr, Inc. | High purity alkoxytrimethylsilane fluids |
| JP2003252879A (ja) * | 2001-12-25 | 2003-09-10 | Nippon Shokubai Co Ltd | アルコキシシランの製造方法 |
| US9263769B2 (en) * | 2014-04-30 | 2016-02-16 | Uchicago Argonne, Llc | Process for the production of low flammability electrolyte solvents |
| MX2017005336A (es) | 2014-10-28 | 2017-08-15 | 3M Innovative Properties Co | Componentes de un sistema de aplicacion por pulverizacion que comprende una superficie repelente y metodos. |
| EP3368618B1 (en) | 2015-10-28 | 2020-11-25 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface |
| BR112018008646A2 (pt) | 2015-10-28 | 2018-10-30 | 3M Innovative Properties Co | componentes de um sistema de aplicação de aspersões que compreende uma superfície repelente e métodos |
| EP3448944A4 (en) | 2016-04-26 | 2019-11-13 | 3M Innovative Properties Company | ARTISTS SUBJECT TO ICE FORMATION WITH A REPELLENT SURFACE COMPRISING SILOXONE MATERIAL |
| CN114524839B (zh) * | 2022-01-12 | 2024-06-25 | 湖北江瀚新材料股份有限公司 | 一种硬脂氧基三甲基硅烷的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1568558A1 (de) * | 1966-07-26 | 1970-03-19 | Bayer Ag | N-Methylolsilylaether |
| US3664937A (en) * | 1968-11-06 | 1972-05-23 | Bayer Ag | Photosensitizing molding and coating compositions with benzoin-silyl-esters |
| US3636026A (en) * | 1968-11-06 | 1972-01-18 | Bayer Ag | Benzoin-silyl-esters |
| GB2009193B (en) * | 1977-11-24 | 1982-03-17 | Dow Corning Ltd | Silylation process |
| DE3911917A1 (de) * | 1989-04-12 | 1990-10-18 | Hoechst Ag | Verfahren zur herstellung von alkoxysilanen, die praktisch frei sind von halogenverbindungen, verwendung dieser alkoxysilane und hydraulische fluessigkeiten, die diese alkoxysilane enthalten |
-
1991
- 1991-10-03 US US07/770,376 patent/US5157139A/en not_active Expired - Lifetime
-
1992
- 1992-09-30 CA CA002079542A patent/CA2079542A1/en not_active Abandoned
- 1992-10-01 DE DE69230989T patent/DE69230989T2/de not_active Expired - Lifetime
- 1992-10-01 EP EP92308942A patent/EP0535947B1/en not_active Expired - Lifetime
- 1992-10-02 TW TW081107846A patent/TW238311B/zh active
- 1992-10-02 KR KR1019920018063A patent/KR100242750B1/ko not_active Expired - Fee Related
- 1992-10-02 AU AU26102/92A patent/AU648200B2/en not_active Ceased
- 1992-10-02 JP JP4264414A patent/JPH05247061A/ja active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023536863A (ja) * | 2020-07-31 | 2023-08-30 | エルジー・ケム・リミテッド | アルコキシシラン化合物の製造方法 |
| JP2023536864A (ja) * | 2020-07-31 | 2023-08-30 | エルジー・ケム・リミテッド | アルコキシシラン化合物の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW238311B (enExample) | 1995-01-11 |
| AU2610292A (en) | 1993-04-08 |
| EP0535947B1 (en) | 2000-05-03 |
| CA2079542A1 (en) | 1993-04-04 |
| US5157139A (en) | 1992-10-20 |
| KR100242750B1 (ko) | 2000-03-02 |
| EP0535947A1 (en) | 1993-04-07 |
| DE69230989D1 (de) | 2000-06-08 |
| AU648200B2 (en) | 1994-04-14 |
| DE69230989T2 (de) | 2000-11-16 |
| KR930007957A (ko) | 1993-05-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH05247061A (ja) | 透明で無色のアルコキシシランモノマーの調製方法 | |
| JPH0689147B2 (ja) | 変性シリコーン化合物及びその製造方法 | |
| JP2000086767A (ja) | 制汗塩用シリコ―ン溶媒 | |
| JPH11255899A (ja) | 一官能価単位および四官能価単位を含有するポリオルガノシロキサン樹脂の製造法 | |
| WO2003091186A2 (en) | Azasilanes and methods for making and using the same | |
| JP3705333B2 (ja) | シラノール基を有する有機けい素化合物の製造方法 | |
| CA2258104C (en) | Process for the preparation of alkoxysilanes | |
| US3555063A (en) | Method for preparing siloxane-polyoxyalkylene copolymers | |
| JP2977218B2 (ja) | シルセスキオキサンの製造方法 | |
| JPH10237177A (ja) | ネットワークポリシランの製造方法 | |
| JP3206384B2 (ja) | アルコキシシロキサンの製造方法 | |
| AU633808B2 (en) | Alkoxy-type derivative compounds and process for preparing alkoxy-type derivatives of trivalent group 3b metals | |
| JP3187444B2 (ja) | オルガノポリシロキサンの製造方法 | |
| JPH04243884A (ja) | 水素シロキサンの製造方法 | |
| JPS6312333A (ja) | 両性界面活性剤の製造法 | |
| JPH06136128A (ja) | リン酸エステルで変性されたオルガノ（ポリ）シロキサン及びその製造方法 | |
| JPH0873474A (ja) | 低重合度オルガノポリシロキサンの製造方法 | |
| JPS6054392A (ja) | 有機けい素化合物のシリル化方法 | |
| JP2880904B2 (ja) | １，１，３，３−テトラメチル−１，３−ジヒドロキシジシロキサンの製造方法 | |
| JP2864191B2 (ja) | スルホン酸変性シリコーン | |
| EP1358191A1 (en) | Process for making silanol stopped oligomeric materials | |
| TW201100440A (en) | Method for producing organoalkoxy hydrogen silanes | |
| JP2668495B2 (ja) | ケイ素系粉末物質の製造方法 | |
| JPH07179479A (ja) | アミドベタイン変性オルガノ（ポリ）シロキサン及びその製造方法 | |
| JP2668496B2 (ja) | ケイ素系粉末物質の新規な製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20020716 |