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444278

Sigma-Aldrich

Decamethylcyclopentasiloxane

97%

Sinónimos:

2,2,4,4,6,6,8,8,10,10-Decamethylcyclopentasiloxane, Cyclic dimethylsiloxane pentamer, Cyclo-decamethylpentasiloxane, Cyclomethicone pentamer 245, Decamethylpentacyclosiloxane

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About This Item

Fórmula empírica (notación de Hill):
C10H30O5Si5
Número de CAS:
541-02-6
Peso molecular:
370.77
Beilstein/REAXYS Number:
1800166
EC Number:
208-764-9
MDL number:
MFCD00046966
UNSPSC Code:
12352103
PubChem Substance ID:
24868110
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.396 (lit.)

bp

90 °C/10 mmHg (lit.)

density

0.958 g/mL at 25 °C (lit.)

SMILES string

C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1

InChI

1S/C10H30O5Si5/c1-16(2)11-17(3,4)13-19(7,8)15-20(9,10)14-18(5,6)12-16/h1-10H3

InChI key

XMSXQFUHVRWGNA-UHFFFAOYSA-N

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General description

Decamethylcyclopentasiloxane (D5) is used in personal care products including skin creams, cosmetics, shampoos, deodorants and conditioners. D5 is also used in various applications such as industrial cleaning fluids and dry cleaning solvents.

Application

Decamethylcyclopentasiloxane (D5) can be used as:
  • A greener solvent in synthetic chemistry applications.
  • A monomeric unit for polymerization by various base catalysts to obtain polysiloxane polymer.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

163.4 °F - closed cup

flash_point_c

73 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Ring-opening polymerization of decamethylcyclopentasiloxane initiated by a superbase: Kinetics and rheology.
Pibre G, et al.
Polymer, 49(1), 234-240 (2008)
Characterization of ecological risks from environmental releases of decamethylcyclopentasiloxane (D5).
Fairbrother A, et al.
Environmental Toxicology and Chemistry / Setac, 34(12), 2715-2722 (2015)
Qiyan Li et al.
Cell biochemistry and function, 32(2), 183-187 (2013-09-03)
Corneal epithelial barrier dysfunction is harmful to corneal health; the pathogenesis is unclear. This study aims to elucidate the mechanism by which tryptase compromises corneal epithelial barrier function. Human corneal epithelial cell line (HCE cells) was cultured into monolayers using
Zhongwang Yu et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 9(24), e2105442-e2105442 (2022-06-28)
Blood-brain barrier (BBB) impairment is an early prevalent feature of multiple sclerosis (MS), and remains vital for MS progression. Microglial activation precedes BBB disruption and cellular infiltrates in the brain of MS patients. However, little is known about the function
Björn F Vahsen et al.
Nature communications, 14(1), 5898-5898 (2023-09-22)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive motor neuron loss, with additional pathophysiological involvement of non-neuronal cells such as microglia. The commonest ALS-associated genetic variant is a hexanucleotide repeat expansion (HRE) mutation in C9orf72. Here, we
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