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169102

Sigma-Aldrich

1-Docosanol

98%

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Synonym(s):
Behenyl alcohol
Linear Formula:
CH3(CH2)21OH
CAS Number:
Molecular Weight:
326.60
Beilstein/REAXYS Number:
1770470
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

assay

98%

bp

180 °C/0.22 mmHg (lit.)

mp

65-72 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCCCCCCO

InChI

1S/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3

InChI key

NOPFSRXAKWQILS-UHFFFAOYSA-N

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1 of 4

This Item
PHR22641312108.22047
vibrant-m

169102

1-Docosanol

vibrant-m

PHR2264

Docosanol (n-Docosanol)

vibrant-m

131210

1-Nonanol

vibrant-m

8.22047

1-Docosanol

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

200

bp

180 °C/0.22 mmHg (lit.)

bp

180 °C/0.22 mmHg (lit.)

bp

215 °C (lit.)

bp

180 °C/0.3 hPa

mp

65-72 °C (lit.)

mp

65-72 °C (lit.)

mp

−8-−6 °C (lit.)

mp

68-71 °C

General description

1-Docosanol inhibits replication of certain viruses (herpes simplex virus and respiratory syncytial virus) within primary target cells in vitro. It has been isolated from Clematis brevicaudata.

Application

1-Docosanol was used in the synthesis of series of amphiphilic dendrimers with hydrophilic aliphatic polyether-type dendritic core and hydrophobic docosyl peripheries.

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

410.0 °F

flash_point_c

210 °C

ppe

Eyeshields, Gloves, type N95 (US)


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Ai-Mei Yang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(10), 1534-1537 (2010-02-02)
To study the chemical constituents from Clematis brevicaudata. The compounds were isolated by column chromatography and their structures were elucidated through spectroscopic analysis (NMR). Eight compounds were isolated and identified as: palmitic acid (1), 1-docosanol (2), pentacosanoic acid-2', 3'-dihydroxypropyl ester
Synthesis and self-assembly of amphiphilic dendrimers based on aliphatic polyether-type dendritic cores.
Cho B-K, et al.
Macromolecules, 37(11), 4227-4234 (2004)
D H Katz et al.
Proceedings of the National Academy of Sciences of the United States of America, 88(23), 10825-10829 (1991-12-01)
This article reports that 1-docosanol, a 22-carbon-long saturated alcohol, exerts a substantial inhibitory effect on replication of certain viruses (e.g., herpes simplex virus and respiratory syncytial virus) within primary target cells in vitro. To study the basis for its viral
Diogo C Morelli et al.
Journal of chromatography. A, 1626, 461377-461377 (2020-08-17)
This study reports the use ofa natural deep eutectic solvent (NADES) with hollow fiber-microporous membrane liquid-liquid microextraction (HF-MMLLE) for the multiclass determination of 11 compounds classified as emerging contaminantsin water. Different deep eutectic solvents were synthetized and Thymol: Camphor (1:1
Kei Watanabe et al.
Journal of oleo science, 61(1), 29-34 (2011-12-23)
In this study, the changes in the structural and physicochemical properties of an α-crystalline phase (often called an "α-gel") were assessed in a sodium methyl stearoyl taurate (SMT)/behenyl alcohol/water system. The α-gels were characterized focusing on the effects of the

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