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M0555

Sigma-Aldrich

Methyl cellulose

26.0-33.0% (Methoxy group (dry basis)), meets USP testing specifications, viscosity: 1,500 cP

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352207
PubChem Substance ID:
NACRES:
NA.71

biological source

synthetic (organic

Organic)

Quality Level

Agency

USP/NF
meets USP testing specifications

Assay

26.0-33.0% (Methoxy group (dry basis))

form

solid

pH

5.0 -8.0

viscosity

1,125-2,100 cP, 2 % in water(20 °C)

application(s)

pharmaceutical (small molecule)

storage temp.

room temp

SMILES string

[*]OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO[*])O[C@@H](O[*])[C@H](O[*])[C@H]2O[*])[C@H](O[*])[C@@H](O[*])[C@@H]1O[*]

InChI key

YLGXILFCIXHCMC-JHGZEJCSSA-N

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Application


  • Flexible Thermoelectric Reduced Graphene Oxide/Ag(2)S/Methyl Cellulose Composite Film Prepared by Screen Printing Process.: This research details the fabrication of a novel composite film incorporating methyl cellulose for enhanced flexibility and thermal electric properties, targeting wearable electronics applications (Wang et al., 2022).

  • Hybrid thermosensitive-mucoadhesive in situ forming gels for enhanced corneal wound healing effect of L-carnosine.: This study utilizes methyl cellulose in a hybrid gel system designed to improve the delivery and efficacy of L-carnosine for corneal wound healing, demonstrating significant therapeutic potential (Fathalla et al., 2022).

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.

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yihua Wang et al.
Biochemistry, 52(9), 1611-1621 (2013-02-07)
Myosin powers contraction in heart and skeletal muscle and is a leading target for mutations implicated in inheritable muscle diseases. During contraction, myosin transduces ATP free energy into the work of muscle shortening against resisting force. Muscle shortening involves relative
Hisham Al-Obaidi et al.
International journal of pharmaceutics, 443(1-2), 95-102 (2013-01-10)
Solid dispersions of varying weight ratios compositions of the nonionic drug, griseofulvin and the hydrophilic, anionic polymer, hydroxylpropylmethyl cellulose acetate succinate, have been prepared by ball milling and the resulting samples characterized using a combination of Fourier transform infra-red spectroscopy
Walter Fuchs et al.
Journal of virology, 83(8), 3930-3943 (2009-02-06)
Cleavage and encapsidation of newly replicated herpes simplex virus type 1 (HSV-1) DNA requires several essential viral gene products that are conserved in sequence within the Herpesviridae. However, conservation of function has not been analyzed in greater detail. For functional
Elsa-Noah N'Diaye et al.
EMBO reports, 10(2), 173-179 (2009-01-17)
Ubiquilins (UBQLNs) are adaptor proteins thought to deliver ubiquitinated substrates to proteasomes. Here, we show a role for UBQLN in autophagy: enforced expression of UBQLN protects cells from starvation-induced death, whereas depletion of UBQLN renders cells more susceptible. The UBQLN
Erik Kaunisto et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(4-5), 698-708 (2013-01-10)
In this paper a new model describing drug release from a polymer matrix tablet is presented. The utilization of the model is described as a two step process where, initially, polymer parameters are obtained from a previously published pure polymer

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