CA1312859C - Derives hydroxypropoxy et methoxy de la cellulose, utiles comme agents epaississants dans des liquides organiques - Google Patents

Derives hydroxypropoxy et methoxy de la cellulose, utiles comme agents epaississants dans des liquides organiques

Info

Publication number: CA1312859C
Authority: CA; Canada
Prior art keywords: percent; substitution; methyl cellulose; hydroxypropyl methyl; methoxyl
Prior art date: 1985-02-28
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 - Fee Related

Application number

CA000615898A

Other languages

English (en)

Inventor

Roland H.P. Hess

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.)

Dow Chemical Europe SA

Dow Chemical Co

Original Assignee

Dow Chemical Europe SA

Dow Chemical Co

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.)

1985-02-28

Filing date

1990-10-17

Publication date

1993-01-19

1985-02-28 Priority claimed from US06/706,829 external-priority patent/US4612345A/en

1985-08-15 Priority claimed from US06/765,788 external-priority patent/US4614545A/en

1986-02-27 Priority claimed from CA000502873A external-priority patent/CA1280413C/fr

1990-10-17 Application filed by Dow Chemical Europe SA, Dow Chemical Co filed Critical Dow Chemical Europe SA

1993-01-19 Application granted granted Critical

1993-01-19 Publication of CA1312859C publication Critical patent/CA1312859C/fr

2006-02-27 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

-1 Hydroxypropyl methyl cellulose ethers Chemical class 0.000 title claims abstract description 85
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 title claims abstract description 85
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 title claims abstract description 85
239000007788 liquid Substances 0.000 title claims abstract description 47
239000001866 hydroxypropyl methyl cellulose Substances 0.000 title claims abstract description 42
239000002562 thickening agent Substances 0.000 title abstract description 21
238000006467 substitution reaction Methods 0.000 claims abstract description 80
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims abstract description 45
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
239000007864 aqueous solution Substances 0.000 claims abstract description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 75
239000000203 mixture Substances 0.000 claims description 17
230000008719 thickening Effects 0.000 claims description 17
238000000034 method Methods 0.000 claims description 12
239000003960 organic solvent Substances 0.000 claims description 11
239000000243 solution Substances 0.000 claims description 8
125000005842 heteroatom Chemical group 0.000 claims description 3
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims 12
150000002170 ethers Chemical class 0.000 abstract description 33
229920002153 Hydroxypropyl cellulose Polymers 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
239000001863 hydroxypropyl cellulose Substances 0.000 abstract 1
235000010977 hydroxypropyl cellulose Nutrition 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 35
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
235000019441 ethanol Nutrition 0.000 description 11
239000002904 solvent Substances 0.000 description 11
HSHXDCVZWHOWCS-UHFFFAOYSA-N N'-hexadecylthiophene-2-carbohydrazide Chemical compound CCCCCCCCCCCCCCCCNNC(=O)c1cccs1 HSHXDCVZWHOWCS-UHFFFAOYSA-N 0.000 description 10
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 10
230000000052 comparative effect Effects 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
229920002678 cellulose Polymers 0.000 description 7
239000001913 cellulose Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
229920003086 cellulose ether Polymers 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
229940050176 methyl chloride Drugs 0.000 description 5
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
239000008186 active pharmaceutical agent Substances 0.000 description 4
229910001854 alkali hydroxide Inorganic materials 0.000 description 4
150000008044 alkali metal hydroxides Chemical class 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000004800 polyvinyl chloride Substances 0.000 description 4
229920000915 polyvinyl chloride Polymers 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
101100424627 Caenorhabditis elegans mec-12 gene Proteins 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000002775 capsule Substances 0.000 description 2
239000000446 fuel Substances 0.000 description 2
239000000499 gel Substances 0.000 description 2
229910052602 gypsum Inorganic materials 0.000 description 2
239000010440 gypsum Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
239000000463 material Substances 0.000 description 2
229920000609 methyl cellulose Polymers 0.000 description 2
239000001923 methylcellulose Substances 0.000 description 2
235000010981 methylcellulose Nutrition 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
239000003973 paint Substances 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
239000002002 slurry Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
238000010557 suspension polymerization reaction Methods 0.000 description 2
KSWPYYWLOGLIIV-UHFFFAOYSA-N 1,4-dioxane pyrrolidin-2-one Chemical compound N1C(CCC1)=O.O1CCOCC1 KSWPYYWLOGLIIV-UHFFFAOYSA-N 0.000 description 1
CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
JBIQBIBOIJBLDZ-UHFFFAOYSA-N 2-ethoxyethanol;1-methoxyethanol Chemical compound COC(C)O.CCOCCO JBIQBIBOIJBLDZ-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
101001098066 Naja melanoleuca Basic phospholipase A2 1 Proteins 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
229920013820 alkyl cellulose Polymers 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
AZHSSKPUVBVXLK-UHFFFAOYSA-N ethane-1,1-diol Chemical compound CC(O)O AZHSSKPUVBVXLK-UHFFFAOYSA-N 0.000 description 1
DHNGCHLFKUPGPX-RMKNXTFCSA-N ethyl trans-p-methoxycinnamate Chemical class CCOC(=O)\C=C\C1=CC=C(OC)C=C1 DHNGCHLFKUPGPX-RMKNXTFCSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
NUKZAGXMHTUAFE-UHFFFAOYSA-N hexanoic acid methyl ester Natural products CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
239000011707 mineral Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
238000013268 sustained release Methods 0.000 description 1
239000012730 sustained-release form Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1

Landscapes

Medicinal Preparation (AREA)

CA000615898A 1985-02-28 1990-10-17 Derives hydroxypropoxy et methoxy de la cellulose, utiles comme agents epaississants dans des liquides organiques Expired - Fee Related CA1312859C (fr)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
US06/706,829 US4612345A (en)	1985-02-28	1985-02-28	Hydroxypropyl methyl cellulose ethers useful as suspending agents for suspension polymerization of vinyl chloride
US706829		1985-02-28
US765788		1985-08-15
US06/765,788 US4614545A (en)	1985-08-15	1985-08-15	Hydroxypropyl methyl cellulose thickening agents for organic liquids
CA000502873A CA1280413C (fr)	1985-02-28	1986-02-27	Esters de l'hydropropylmethyl cellulose utiles comme agents de mise en suspension pour la polymerisation de suspensions de chlorure de vinyle, et comme epaississants pour les liquides organiques

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000502873A Division CA1280413C (fr)	1985-02-28	1986-02-27	Esters de l'hydropropylmethyl cellulose utiles comme agents de mise en suspension pour la polymerisation de suspensions de chlorure de vinyle, et comme epaississants pour les liquides organiques

Publications (1)

Publication Number	Publication Date
CA1312859C true CA1312859C (fr)	1993-01-19

Family

ID=27167589

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000615898A Expired - Fee Related CA1312859C (fr)	1985-02-28	1990-10-17	Derives hydroxypropoxy et methoxy de la cellulose, utiles comme agents epaississants dans des liquides organiques

Country Status (1)

Country	Link
CA (1)	CA1312859C (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN112438945A (zh) *	2020-11-30	2021-03-05	北方天普纤维素有限公司	免洗消毒凝胶及其制备方法

1990
- 1990-10-17 CA CA000615898A patent/CA1312859C/fr not_active Expired - Fee Related

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN112438945A (zh) *	2020-11-30	2021-03-05	北方天普纤维素有限公司	免洗消毒凝胶及其制备方法

Legal Events

Date	Code	Title	Description
1995-07-19	MKLA	Lapsed

Publication	Publication Date	Title
US4614545A (en)	1986-09-30	Hydroxypropyl methyl cellulose thickening agents for organic liquids
US5292877A (en)	1994-03-08	Cellulose acetoacetates
CA1307258C (fr)	1992-09-08	Hydroxycellulose a groupes carboxymethyl, hydrophobiquement modifiee (cmhmhec),et son utilisation dans des compositions de revetements protecteurs
US4096326A (en)	1978-06-20	Dihydroxypropyl cellulose
AU656800B2 (en)	1995-02-16	Adhesive stick made from starch ethers
US3709876A (en)	1973-01-09	Water soluble hydroxyethyl methyl cellulose ether thickener for latex paint
DE69010350T2 (de)	1994-11-17	Polysaccharide mit Alkaryl- oder Aralkyl- Hydrophoben und Latexzusammensetzungen, die die Polysaccharide enthalten.
US3493407A (en)	1970-02-03	Preparation of medicinal capsules from hydroxyalkylcellulose ethers
US3629237A (en)	1971-12-21	Compositions useful as enteric coatings and method for preparing acid phthalates of cellulose ethers for them
CA2011848C (fr)	1996-10-01	Ethers cellulosiques non ioniques solubles dans l'eau pour peintures
JP2950868B2 (ja)	1999-09-20	水溶性セルロースエーテルポリマー
JPH08509755A (ja)	1996-10-15	多糖類脂肪酸エステルの応用と製造方法
DE69820933T2 (de)	2004-11-04	Biostabile, wässrige Lacke und Verfahren zur deren Herstellung
DE1568423A1 (de)	1970-03-19	Neuartige Hydroxypropylmethylcelluloseaether,Verfahren zur Herstellung derselben und Massen,in denen solche AEther verwendet werden
JP2001520297A (ja)	2001-10-30	疎水変性ポリ（アセタール−またはケタール−ポリエーテル）、ポリウレタンおよびポリアクリレートの流動化ポリマー懸濁液
EP0761690A1 (fr)	1997-03-12	Polysaccharides esters ou éther esters thermoplastiques et biodégradables résultant de la réaction avec des produits d'addition d'acide maléique
US4906744A (en)	1990-03-06	Water-soluble ethers substituted with alkenyl or alkyl succinic acid esters
EP0573852B1 (fr)	1997-12-17	Alkylhydroxyalkylcellulose contenant des groupes sulfoéthyle
EP0426086A1 (fr)	1991-05-08	Ethers de cellulose modifiés par des groupes alkylaryl hydrophobes
JPS61264001A (ja)	1986-11-21	ヒドロキシプロピルメチルセルロ−スエ−テル
EP0048556B1 (fr)	1984-12-27	Composition pâteuse contenant un hydrocolloide
CA2347839A1 (fr)	2000-05-11	Combinaisons d'epaississants associatifs et de compositions aqueuses de revetement protecteur
EP0353789A1 (fr)	1990-02-07	Hydroxypropylméthylcellulose utile comme agent épaississant pour des liquides organiques
US4097667A (en)	1978-06-27	Hydroxyalkyl cellulose ethers
US5166333A (en)	1992-11-24	Methyl hydroxypropyl cellulose ethers and a process for their production

CA1312859C - Derives hydroxypropoxy et methoxy de la cellulose, utiles comme agents epaississants dans des liquides organiques - Google Patents

Info

Links

Landscapes

Applications Claiming Priority (5)

Related Parent Applications (1)

Publications (1)

Family

ID=27167589

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Similar Documents

Legal Events