GB1300696A - Method of preparing cellulose ether derivatives - Google Patents
Method of preparing cellulose ether derivativesInfo
- Publication number
- GB1300696A GB1300696A GB23320/71A GB2332071A GB1300696A GB 1300696 A GB1300696 A GB 1300696A GB 23320/71 A GB23320/71 A GB 23320/71A GB 2332071 A GB2332071 A GB 2332071A GB 1300696 A GB1300696 A GB 1300696A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- hydroxyalkyl
- anhydride
- groups per
- ether
- 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
- 229920003086 cellulose ether Polymers 0.000 title abstract 4
- 150000002170 ethers Chemical class 0.000 title 1
- -1 hydroxyalkyl ethers Chemical class 0.000 abstract 7
- 229920002678 cellulose Polymers 0.000 abstract 4
- 239000001913 cellulose Substances 0.000 abstract 4
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical group OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 abstract 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 239000004135 Bone phosphate Substances 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B13/00—Preparation of cellulose ether-esters
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP45019553A JPS4819231B1 (enExample) | 1970-03-06 | 1970-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1300696A true GB1300696A (en) | 1972-12-20 |
Family
ID=12002492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23320/71A Expired GB1300696A (en) | 1970-03-06 | 1971-04-19 | Method of preparing cellulose ether derivatives |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3712886A (enExample) |
| JP (1) | JPS4819231B1 (enExample) |
| DE (1) | DE2110546C3 (enExample) |
| FR (1) | FR2084229A5 (enExample) |
| GB (1) | GB1300696A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100453557C (zh) * | 2003-02-19 | 2009-01-21 | 北京理工大学 | 纤维素甘油醚硝酸酯的制备方法 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3870702A (en) * | 1971-03-19 | 1975-03-11 | Shinetsu Chemical Co | Cellulose ether compositions useful as enteric coatings |
| US3839319A (en) * | 1973-01-26 | 1974-10-01 | Dow Chemical Co | Hydroxypropyl methylcellulose ethers and method of preparation |
| US4001211A (en) * | 1974-12-02 | 1977-01-04 | The Dow Chemical Company | Pharmaceutical capsules from improved thermogelling methyl cellulose ethers |
| US4226981A (en) * | 1977-09-28 | 1980-10-07 | Shin-Etsu Chemical Co., Ltd. | Ether-ester derivatives of cellulose and their applications |
| US4383988A (en) * | 1978-04-28 | 1983-05-17 | Anheuser-Busch, Incorporated | Gelled antiperspirant |
| US5188666A (en) * | 1983-06-30 | 1993-02-23 | Boccardo Victor N | Paint removing compositions and methods for the manufacture and use thereof |
| US4609729A (en) * | 1985-04-03 | 1986-09-02 | The Dow Chemical Company | Organosoluble C3 -C4 hydroxyalkyl ethyl cellulose ethers |
| US5656746A (en) * | 1996-03-28 | 1997-08-12 | The Proctor & Gamble Company | Temporary wet strength polymers from oxidized reaction product of polyhydroxy polymer and 1,2-disubstituted carboxylic alkene |
| US5698688A (en) * | 1996-03-28 | 1997-12-16 | The Procter & Gamble Company | Aldehyde-modified cellulosic fibers for paper products having high initial wet strength |
| DE19959419A1 (de) * | 1999-12-09 | 2001-06-21 | Ratiopharm Gmbh | Stabile galenische Zubereitungen umfassend ein Benzimidazol und Verfahren zu ihrer Herstellung |
| JP6267239B2 (ja) * | 2013-03-07 | 2018-01-24 | ダウ グローバル テクノロジーズ エルエルシー | 極めて低粘度の新規エステル化セルロースエーテル |
-
1970
- 1970-03-06 JP JP45019553A patent/JPS4819231B1/ja active Pending
-
1971
- 1971-02-24 US US00118555A patent/US3712886A/en not_active Expired - Lifetime
- 1971-03-05 FR FR7107647A patent/FR2084229A5/fr not_active Expired
- 1971-03-05 DE DE2110546A patent/DE2110546C3/de not_active Expired
- 1971-04-19 GB GB23320/71A patent/GB1300696A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100453557C (zh) * | 2003-02-19 | 2009-01-21 | 北京理工大学 | 纤维素甘油醚硝酸酯的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4819231B1 (enExample) | 1973-06-12 |
| US3712886A (en) | 1973-01-23 |
| DE2110546C3 (de) | 1982-03-25 |
| FR2084229A5 (enExample) | 1971-12-17 |
| DE2110546B2 (de) | 1981-05-14 |
| DE2110546A1 (de) | 1971-09-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |