1-PENTADECANOL
1-PENTADECANOL Basic information
- Product Name:
- 1-PENTADECANOL
- Synonyms:
-
- N-PENTADECANOL
- N-PENTADECYL ALCOHOL
- PENTADECANOL
- PENTADECYL ALCOHOL
- n-1-Pentadecanol
- Neodol 5
- pentadecan-1-ol
- Pentadecanol-(1)
- CAS:
- 629-76-5
- MF:
- C15H32O
- MW:
- 228.41
- EINECS:
- 211-107-9
- Product Categories:
-
- 1-Alkanols
- Biochemistry
- Higher Fatty Acids & Higher Alcohols
- Monofunctional & alpha,omega-Bifunctional Alkanes
- Monofunctional Alkanes
- Saturated Higher Alcohols
- Mol File:
- 629-76-5.mol
1-PENTADECANOL Chemical Properties
- Melting point:
- 41-44 °C (lit.)
- Boiling point:
- 269-271 °C
- Density
- 0.8364 g/cm3 (22.4℃)
- refractive index
- 1.4507 (589.3 nm 0℃)
- Flash point:
- >230 °F
- storage temp.
- Refrigerator
- solubility
- Chloroform, Methanol (Slightly)
- pka
- 15.20±0.10(Predicted)
- form
- Solid
- color
- White to Off-White
- Water Solubility
- Insoluble in water.
- BRN
- 1700695
- InChIKey
- REIUXOLGHVXAEO-UHFFFAOYSA-N
- LogP
- 6.443 (est)
- CAS DataBase Reference
- 629-76-5(CAS DataBase Reference)
- EPA Substance Registry System
- 1-Pentadecanol (629-76-5)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- TSCA
- Yes
- HS Code
- 29051900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1-PENTADECANOL Usage And Synthesis
Chemical Properties
white solid
Uses
1-Pentadecanol is a fatty alcohol found in myrrh and frankincense essential oils.
Uses
1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B.
Definition
ChEBI: A long-chain fatty alcohol that is pentadecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group
General Description
Colorless liquid with a faint odor of alcohol. Floats on water.
Reactivity Profile
1-PENTADECANOL is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.
Health Hazard
Low toxicity. Excessive exposure produces some central nervous system depression. Prolonged contact produces skin irritation.
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1-PENTADECANOL(629-76-5)Related Product Information
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