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Merck

08066

Oleyl alcohol

analytical standard

Synonym(s):

Z-9-Dodecen-1-ol, cis-9-Octadecen-1-ol

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About This Item

Linear Formula:
CH3(CH2)7CH=CH(CH2)7CH2OH
CAS Number:
Molecular Weight:
268.48
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-597-3
Beilstein/REAXYS Number:
1723962
MDL number:
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Product Name

Oleyl alcohol, analytical standard

InChI key

ALSTYHKOOCGGFT-KTKRTIGZSA-N

InChI

1S/C18H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h9-10,19H,2-8,11-18H2,1H3/b10-9-

SMILES string

CCCCCCCC\C=C/CCCCCCCCO

grade

analytical standard

assay

≥90.0% (GC)

shelf life

limited shelf life, expiry date on the label

impurities

≤0.5% water

refractive index

n20/D 1.457-1.462
n20/D 1.46 (lit.)

bp

207 °C/13 mmHg (lit.)

mp

0-5.0 °C (lit.)

density

0.849 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

−20°C

Quality Level

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Storage Class

10 - Combustible liquids

wgk

awg

flash_point_f

338.0 °F - closed cup

flash_point_c

170 °C - closed cup


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Contact dermatitis due to oleyl alcohol.
M S Guidetti et al.
Contact dermatitis, 31(4), 260-261 (1994-10-01)
Takayuki Sato et al.
Chemical & pharmaceutical bulletin, 63(2), 88-94 (2015-03-10)
The purpose of this study was to characterize the non-aqueous nanosuspension of a hydrophilic drug prepared by bead milling for cutaneous application. Riboflavin was used as the model hydrophilic drug. The non-aqueous nanosuspensions were prepared by grinding riboflavin with zirconia
Marie Takai et al.
Bioscience, biotechnology, and biochemistry, 78(2), 238-244 (2014-07-19)
Transmembrane protein CD36 binds multiple ligands, including oxidized low-density lipoproteins (oxLDLs) and long-chain fatty acids (LCFAs). Our aim was to determine whether LCFAs compete with oxLDLs for binding to CD36. We addressed this issue by examining the inhibitory effect of

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