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369314

Sigma-Aldrich

Oleyl alcohol

technical grade, 85%

Sinónimos:

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

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About This Item

Fórmula lineal:
CH3(CH2)7CH=CH(CH2)7CH2OH
Número de CAS:
143-28-2
Peso molecular:
268.48
Beilstein:
1723962
Número CE:
205-597-3
Número MDL:
MFCD00002993
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
24862955
NACRES:
NA.22

grado

technical grade

Análisis

85%

formulario

liquid

índice de refracción

n20/D 1.46 (lit.)

bp

207 °C/13 mmHg (lit.)

mp

0-5.0 °C (lit.)

densidad

0.849 g/mL at 25 °C (lit.)

cadena SMILES

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-

Clave InChI

ALSTYHKOOCGGFT-KTKRTIGZSA-N

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Descripción general

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.

Aplicación

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

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

awg

Punto de inflamabilidad (°F)

338.0 °F - closed cup

Punto de inflamabilidad (°C)

170 °C - closed cup

Equipo de protección personal

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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USP

USP

1367699

Linolenyl alcohol

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

Stearyl alcohol United States Pharmacopeia (USP) Reference Standard

USP

1622000

Stearyl alcohol

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
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
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
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
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
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