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Merck
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Documentos

169102

Sigma-Aldrich

1-Docosanol

98%

Sinónimos:

Behenyl alcohol

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About This Item

Fórmula lineal:
CH3(CH2)21OH
Número de CAS:
661-19-8
Peso molecular:
326.60
Beilstein/REAXYS Number:
1770470
EC Number:
211-546-6
MDL number:
MFCD00002939
UNSPSC Code:
12352100
PubChem Substance ID:
24850264
NACRES:
NA.22

Quality Level

200

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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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)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Arachidyl alcohol United States Pharmacopeia (USP) Reference Standard

USP

1042270

Arachidyl alcohol

1-Triacontanol ≥98% (capillary GC)

Sigma-Aldrich

T3777

1-Triacontanol

1-Octadecanol Selectophore™, ≥99.0%

Supelco

74723

1-Octadecanol

1-Nonadecanol 99%

Sigma-Aldrich

286842

1-Nonadecanol

Behenic acid 99%

Sigma-Aldrich

216941

Behenic acid

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
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)
Guadalupe Iglesias et al.
Regulatory toxicology and pharmacology : RTP, 36(1), 80-85 (2002-10-18)
Behenyl alcohol is a saturated 22-carbon, long-chain aliphatic alcohol, which has potential for use in foods as an oil-structuring and -solidifying agent in fats. Previously completed studies with behenyl alcohol indicated an absence of mutagenic or genotoxic potential. In addition
John F Marcelletti
Antiviral research, 56(2), 153-166 (2002-10-09)
Interactions between docosanol (n-docosanol, behenyl alcohol) and nucleoside or pyrophosphate analogs were investigated in vitro. The anti-HSV activity of acyclovir (ACV) was synergistically enhanced by treatment of cells with docosanol as judged by inhibition of progeny virus production and plaque
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
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