n-Docosanol

n-Docosanol
  • CAS No.:661-19-8
Other grades of this product :
n-Docosanol Basic information
Product Name:n-Docosanol
Synonyms:ALCOHOL C22;BEHENYLIC ALCOHOL;Behenic alcohol;behenicalcohol;Cachalot BE-22;Dehydag wax 22 (lanette);Docosan-1-ol;Docosanol-(1)
CAS:661-19-8
MF:C22H46O
MW:326.6
EINECS:211-546-6
Product Categories:ABREVA;Pharmaceutical Raw Materials;Saturated Higher Alcohols;1-Alkanols;Antivirals for Research and Experimental Use;Biochemistry;Higher Fatty Acids & Higher Alcohols;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes;Pharma material;fine chemicals;Inhibitors;661-19-8
Mol File:661-19-8.mol
n-Docosanol Chemical Properties
Melting point 65-72 °C(lit.)
Boiling point 180 °C0.22 mm Hg(lit.)
density d75 0.8063 g/ml; d85 0.7986 g/ml; d95 0.7911 g/ml
vapor pressure 0Pa at 25℃
refractive index n75 1.4360
storage temp. Store below +30°C.
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
pka15.20±0.10(Predicted)
form Pellets or Tablets
color White
Water Solubility Insoluble
Merck 13,3433
BRN 1770470
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
LogP8.3 at 20℃
CAS DataBase Reference661-19-8(CAS DataBase Reference)
NIST Chemistry Reference1-Docosanol(661-19-8)
EPA Substance Registry System1-Docosanol (661-19-8)
Safety Information
Safety Statements 24/25
WGK Germany -
RTECS JR1315000
TSCA Yes
HS Code 29051900
Hazardous Substances Data661-19-8(Hazardous Substances Data)
ToxicityLD50 intraperitoneal in mouse: > 800mg/kg
MSDS Information
ProviderLanguage
1-Docosanol English
ACROS English
SigmaAldrich English
ALFA English
n-Docosanol Usage And Synthesis
Chemical Properties1-DOCOSANOL is white powder
Usesantiviral
Usesn-Docosanol is a binder and an emulsion stabilizer. It is also used to increase a formulation’s viscosity. This is a mixture of fatty alcohols. behenyl alcohol may be used for any number of purposes in a cosmetic formulation, including as an emollient, a binder, an emulsion stabilizer, or to increase a product’s viscosity. It may be derived either synthetically or from plants.
Uses1-Docosanol works as a surfactant in cosmetics. 1-Docosanol cream has also been approved by the US Food and Drug Administration as a safe and effective topical treatment for herpes labialis
IndicationsDocosanol (Abreva) is a long-chain saturated alcohol that is clinically effective against HSV. It has in vitro activity against many enveloped viruses, including CMV, influenzavirus, and respiratory syncytial virus. Docosanol is not directly virucidal; instead, it blocks the entry of the virion into the host cell by inhibiting the fusion of the viral envelope with the host plasma membrane. Because it does not affect viral replication or protein production, it may be less susceptible to the development of resistance than other antiviral drugs.
Definition1-DOCOSANOL is a long-chain, saturated fatty alcohol.
General Description1-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.
Flammability and ExplosibilityNotclassified
Pharmaceutical Applications1-DOCOSANOL is a 22-carbon straight chain alcohol licensed for over-thecounter sales for the topical treatment of herpes labialis. It is thought to act by blocking viral fusion with the host cell, although definitive studies are lacking. The clinical relevance of the antiviral activity has been debated and the place of this medication as a treatment of herpes labialis remains to be established.
Clinical UseDocosanol cream is approved for the over-the-counter treatment of herpes labialis. It shortens the duration of symptoms of cold sores and fever blisters but does not provide symptomatic relief.
Side effectsAdverse effects of docosanol are minimal. Skin irritation occurs infrequently. Drug interactions are not anticipated.
Purification MethodsCrystallise docosanol from ether or chloroform/ether. [Beilstein 1 IV 1906.]
n-Docosanol Preparation Products And Raw materials
Preparation ProductsN-TETRATETRACONTANE

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