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H9262

Sigma-Aldrich

(Hydroxypropyl)methyl cellulose

viscosity 80-120 cP, 2 % in H2O(20 °C)(lit.)

Synonym(s):

2-Hydroxypropyl methyl cellulose ether

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.56

form

powder

Quality Level

mol wt

~26 kDa

color

beige

viscosity

80-120 cP, 2 % in H2O(20 °C)(lit.)

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Application

(Hydroxypropyl)methyl cellulose acts as a thickener for aqueous and non-aqueous systems, is a water retention aid and steric stabilizer, and clear films with grease resistance. (Hydroxypropyl)methyl cellulose has been used to study mucoadhesion in the design of drug delivery systems to prolong intestinal residence time and has also been used to study the enhancement of dissolution rate of poorly water soluble drugs.
Thickener for aqueous and non-aqueous systems, clear films with grease resistance, binders, lubricants, steric stabilizer and water retention aid.

Features and Benefits

Dissolves in water, undergoes reversible gelation upon heating, non-ionic, does not complex with ionic species and is surface active and enzyme resistant. Solutions are pseudoplastic.

Other Notes

To gain a comprehensive understanding of our extensive range of Polysaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Deirdre M D'Arcy et al.
AAPS PharmSciTech, 20(2), 47-47 (2019-01-09)
Viscosity, influenced by medium composition, will affect the hydrodynamics of a dissolution system. Dissolution simulation methods are valuable tools to explore mechanistic dissolution effects, with an understanding of limitations of any simulation method essential to its appropriate use. The aims
Lucas Sievens-Figueroa et al.
International journal of pharmaceutics, 423(2), 496-508 (2011-12-20)
The design and feasibility of a simple process of incorporating stable nanoparticles into edible polymer films is demonstrated with the goal of enhancing the dissolution rate of poorly water soluble drugs. Nanosuspensions produced from wet stirred media milling (WSMM) were
Michelle Lay Teng Ang et al.
Infection and immunity, 82(5), 1850-1859 (2014-02-26)
Tuberculosis remains a major worldwide epidemic because of its sole etiological agent, Mycobacterium tuberculosis. Ethionamide (ETH) is one of the major antitubercular drugs used to treat infections with multidrug-resistant M. tuberculosis strains. ETH is a prodrug that requires activation within
Takuya Ogawa et al.
The FEBS journal, 281(14), 3165-3176 (2014-05-23)
Saturation of a prenyl group to various levels is a frequently observed modification of isoprenoids. The members of the geranylgeranyl reductase family, however, are the only known enzymes responsible for such reductive modifications in archaea. A methanogenic archaeon, Methanosarcina acetivorans
Francis W Hunter et al.
Biochemical pharmacology, 89(2), 224-235 (2014-03-19)
The nitro-chloromethylbenzindoline prodrug SN29428 has been rationally designed to target tumour hypoxia. SN29428 is metabolised to a DNA minor groove alkylator via oxygen-sensitive reductive activation initiated by unknown one-electron reductases. The present study sought to identify reductases capable of activating

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