| Identification | More | [Name]
1-PENTADECANOL | [CAS]
629-76-5 | [Synonyms]
1-PENTADECANOL
ALCOHOL C15
N-PENTADECANOL
N-PENTADECYL ALCOHOL
PENTADECANOL
PENTADECYL ALCOHOL
n-1-Pentadecanol
Neodol 5
pentadecan-1-ol
Pentadecanol-(1)
Pentadecanol,95%
1-PENTADECANOL, 99+%
1-PENTADECANOL 97+%
1-PENTADECANOL 95+% | [EINECS(EC#)]
211-107-9 | [Molecular Formula]
C15H32O | [MDL Number]
MFCD00004759 | [Molecular Weight]
228.41 | [MOL File]
629-76-5.mol |
| Chemical Properties | Back Directory | [Appearance]
white solid | [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℃) | [Fp ]
>230 °F
| [storage temp. ]
Refrigerator | [solubility ]
Chloroform, Methanol (Slightly) | [form ]
Solid | [pka]
15.20±0.10(Predicted) | [color ]
White to Off-White | [Odor]
Very faint, bland-waxy and discretely floral odor of excellent tenacity | [Water Solubility ]
Insoluble in water. | [BRN ]
1700695 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - EMOLLIENT
EMULSION STABILISING | [InChI]
1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3 | [InChIKey]
REIUXOLGHVXAEO-UHFFFAOYSA-N | [SMILES]
CCCCCCCCCCCCCCCO | [LogP]
6.443 (est) | [CAS DataBase Reference]
629-76-5(CAS DataBase Reference) | [EPA Substance Registry System]
1-Pentadecanol (629-76-5) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H413 | [Precautionary statements ]
P501-P273 | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29051900 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [General Description]
Colorless liquid with a faint odor of alcohol. Floats on water. | [Reactivity Profile]
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. | [Chemical Properties]
white solid | [Uses]
1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B. | [Uses]
1-Pentadecanol is a fatty alcohol found in myrrh and frankincense essential oils. | [Definition]
ChEBI: A long-chain fatty alcohol that is pentadecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group | [Preparation]
via Myristic acid and the Cyanide
(Pentadecanoic nitrile) to the Pentadecanoic
acid via Ethylester and reduction to the title
alcohol. | [storage]
Store at -20°C | [References]
[1] K. Venkatesan, K.V. Srinivasan. “A novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol.” Tetrahedron, asymmetry 19 2 (2008): Pages 209-215. |
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J & K SCIENTIFIC LTD.
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Energy Chemical
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Maya High Purity Chemicals
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