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369314

Sigma-Aldrich

Oleylalkohol

technical grade, 85%

Synonym(e):

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

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About This Item

Lineare Formel:
CH3(CH2)7CH=CH(CH2)7CH2OH
CAS-Nummer:
143-28-2
Molekulargewicht:
268.48
Beilstein:
1723962
EG-Nummer:
205-597-3
MDL-Nummer:
MFCD00002993
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24862955
NACRES:
NA.22

Qualität

technical grade

Assay

85%

Form

liquid

Brechungsindex

n20/D 1.46 (lit.)

bp

207 °C/13 mmHg (lit.)

mp (Schmelzpunkt)

0-5.0 °C (lit.)

Dichte

0.849 g/mL at 25 °C (lit.)

SMILES String

CCCCCCCC\C=C/CCCCCCCCO

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-

InChIKey

ALSTYHKOOCGGFT-KTKRTIGZSA-N

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Allgemeine Beschreibung

Oleyl alcohol has been reported as an effective solvent for oil/water-type tacrolimus (FK506) cream formulation, useful for atopic dermatitis treatment. It was reported as diluting agent for Alamine 336. Palm oil esters derived from oleyl alcohol, have potential applications in the cosmetic and pharmaceutical industries due to the excellent wetting behavior of the esters without the oily feel.

Anwendung

Oleyl alcohol may be employed as solvent during butanol production from corn stover hydrolysates (CSH) with in-situ liquid-liquid extraction.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

awg

Flammpunkt (°F)

338.0 °F - closed cup

Flammpunkt (°C)

170 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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USP

USP

1367699

9,12,15-Octadecatrienol

1-Octadecanol 95%

Sigma-Aldrich

O709

1-Octadecanol

Stearyl alcohol for synthesis

Sigma-Aldrich

8.07680

Stearyl alcohol

Decanal natural, ≥97%, FG

Sigma-Aldrich

W236217

Decanal

Stearylalkohol United States Pharmacopeia (USP) Reference Standard

USP

1622000

Stearylalkohol

Müge Gökdere et al.
Preparative biochemistry & biotechnology, 44(1), 80-89 (2013-10-15)
Gibberelic acid fermentation using extractive methods was carried out in the presence of corn oil and Alamine 336. Gibberella fujikuroi fungus (NRRL 2278) was used to produce gibberellic acid. Oleyl alcohol was a diluting agent for Alamine 336. The effects
Sook Han Ng et al.
Journal of nanobiotechnology, 11, 27-27 (2013-09-26)
Palm oil esters (POEs) are esters derived from palm oil and oleyl alcohol have great potential in the cosmetic and pharmaceutical industries due to the excellent wetting behavior of the esters without the oily feel. The role of oil-in-water nanoemulsions
Fengqin Wang et al.
Sheng wu gong cheng xue bao = Chinese journal of biotechnology, 29(10), 1515-1526 (2014-01-18)
Butanol production from corn stover hydrolysates (CSH) with in-situ liquid-liquid extraction was studied to enhance the production and reduce the fermentation cost. Oleyl alcohol was selected as the suitable solvent and added at the initial fermentation time with the ratio
George M Teke et al.
Biotechnology and bioengineering, 118(1), 58-71 (2020-09-03)
Extractive fermentation (or in situ product removal (ISPR)) is an operational method used to combat product inhibition in fermentations. To achieve ISPR, different separation techniques, modes of operation and physical reactor configurations have been proposed. However, the relative paucity of
Masayuki Yamanaka et al.
International journal of pharmaceutics, 464(1-2), 19-26 (2014-01-25)
We developed an oil/water-type tacrolimus (FK506) cream formulation as an alternative to Protopic ointment for atopic dermatitis treatment. We determined the effects of solvents used in topical preparations on FK506 solubility and stability, and evaluated FK506 transdermal absorption into rat
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