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Merck
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Documentos

93547

Supelco

Farnesol

mixture of isomers, analytical standard

Sinónimos:

3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol

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About This Item

Fórmula lineal:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2CH2C(CH3)=CHCH2OH
Número de CAS:
4602-84-0
Peso molecular:
222.37
Beilstein/REAXYS Number:
1763926
EC Number:
225-004-1
MDL number:
MFCD00002918
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

composition

2Z,6Z, 4.0-6.0% GC
2Z,6E, 8.0-12.0% GC
2E,6Z, 12.0-18.0% GC
2E,6E, 62.0-72.0% GC

refractive index

n20/D 1.487-1.493
n20/D 1.489 (lit.)

bp

149 °C/4 mmHg (lit.)

density

0.886 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

C/C(CC/C=C(C)/CCC=C(C)C)=C\CO

InChI

1S/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3/b14-9+,15-11+

InChI key

CRDAMVZIKSXKFV-YFVJMOTDSA-N

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pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1B

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

311.0 °F - closed cup

flash_point_c

155 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number
BCCG4703
BCCB4179
BCBS5514

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Young Yun Jung et al.
Molecules (Basel, Switzerland), 23(11) (2018-11-06)
Farnesol, an acyclic sesquiterpene alcohol, is predominantly found in essential oils of various plants in nature. It has been reported to exhibit anti-cancer and anti-inflammatory effects, and also alleviate allergic asthma, gliosis, and edema. In numerous tumor cell lines, farnesol
Carla Cugini et al.
Molecular microbiology, 65(4), 896-906 (2007-07-21)
Farnesol is a sesquiterpene produced by many organisms, including the fungus Candida albicans. Here, we report that the addition of farnesol to cultures of Pseudomonas aeruginosa, an opportunistic human bacterial pathogen, leads to decreased production of the Pseudomonas quinolone signal
J Pablo Lamas et al.
Journal of chromatography. A, 1217(12), 1882-1890 (2010-02-09)
Fragrances are ubiquitous pollutants in the environment, present in the most of household products, air fresheners, insecticides and cosmetics. Commercial perfumes may contain hundreds of individual fragrance chemicals. In addition to the widespread use and exposure to fragranced products, many

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