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27483

Supelco

(−)-β-Citronellol

analytical standard

Synonym(s):

β-Rhodinol, (S)-(−)-β-Citronellol, (S)-3,7-Dimethyl-6-octen-1-ol

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About This Item

Empirical Formula (Hill Notation):
C10H20O
CAS Number:
Molecular Weight:
156.27
Beilstein:
1721505
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98.5% (sum of enantiomers, GC)

optical activity

[α]20/D −5.3±0.2°, neat

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.456

bp

221-224 °C

density

0.854 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@H](CCO)CC\C=C(\C)C

InChI

1S/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h5,10-11H,4,6-8H2,1-3H3/t10-/m0/s1

InChI key

QMVPMAAFGQKVCJ-JTQLQIEISA-N

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General description

Citronellol is a monoterpene alcohol found in essential oils of Cymbopogon winterianus Jowitt. S-(−)-isomer that is less common. It is prevalent in geranium and citronella oils.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Chiral building block

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

213.8 °F - DIN 51758

Flash Point(C)

101 °C - DIN 51758

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Customers Also Viewed

K. Mori et al.
Liebigs Ann. Chem., 717-717 (1988)
Study of anticonvulsant effect of citronellol, a monoterpene alcohol, in rodents.
de Sousa DP, et al.
Neuroscience Letters, 401(3), 231-235 (2006)
Yoshikazu Kitano et al.
Biofouling, 27(2), 201-205 (2011-02-01)
Twenty novel simple alkyl isocyanides derived from citronellol were synthesized and evaluated for their antifouling activity and toxicity against cypris larvae of the barnacle, Balanus amphitrite. The anti-barnacle activity of the synthesized isocyanides was in the EC(50) range of 0.08-1.49
Michiko Katsukawa et al.
Bioscience, biotechnology, and biochemistry, 75(5), 1010-1012 (2011-05-21)
We evaluated the effects of rose oil on the peroxisome proliferator-activated receptor (PPAR) and cyclooxygenase-2 (COX-2). Citronellol and geraniol, the major components of rose oil, activated PPARα and γ, and suppressed LPS-induced COX-2 expression in cell culture assays, although the
Renan G Brito et al.
Journal of natural medicines, 66(4), 637-644 (2012-02-22)
We describe the antinociceptive and anti-inflammatory properties of citronellol (CT) in rodents. CT, a monoterpene alcohol, is a naturally occurring monoterpene compound prevalent in essential oils of various aromatic plant species, such as Cymbopogon citratus. In mice, when evaluated against

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