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303488

Sigma-Aldrich

(S)-(−)-β-Citronellol

≥97%

Synonym(s):

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

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About This Item

Linear Formula:
(CH3)2C=CHCH2CH2CH(CH3)CH2CH2OH
CAS Number:
7540-51-4
Molecular Weight:
156.27
Beilstein:
1721505
EC Number:
231-415-7
MDL number:
MFCD00063214
UNSPSC Code:
12352104
PubChem Substance ID:
24858126
NACRES:
NA.22

vapor pressure

~0.02 mmHg ( 25 °C)

Assay

≥97%

form

liquid

optical activity

[α]20/D −4.5°, neat

refractive index

n20/D 1.456 (lit.)

bp

225-226 °C (lit.)

density

0.856 g/mL at 25 °C (lit.)

functional group

hydroxyl

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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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H319

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)

Lot/Batch Number
SHBM6453
MKCC2921
MKBT0974V
MKBH6198V
MKBF5170

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Hyland Cronin et al.
Journal of cosmetic dermatology, 9(3), 218-225 (2010-10-05)
New developments in the realm of skin rejuvenation such as phytotherapy are at an astounding increasing pace in the cosmeceutical market. Yet, many of these products that are classified as cosmeceuticals are tested less vigorously and do not have to
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
Shalinder Kaur et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 66(5-6), 260-266 (2011-08-05)
Citronellol, an oxygenated monoterpene, is found naturally in the essential oils of several aromatic plants and has been reported to exhibit growth inhibitory and pesticidal activities. However, its mechanism of action is largely unexplored. We investigated the effect of citronellol
Aimi Aishah Arifin et al.
Bioresource technology, 102(19), 9318-9320 (2011-08-13)
The present work aims to address the gas-phase biotransformation of geraniol into citronellol using growing cells of Saccharomyces cerevisiae (baker's yeast) in a continuous-closed-gas-loop bioreactor (CCGLB). This study revealed that the gaseous geraniol had a severe effect on the production
Gajanan B Zore et al.
Mycoses, 54(4), e99-109 (2010-03-27)
Fluconazole (FLC) susceptibility of isolates of Candida spp., (n = 42) and efficacy as well as mechanism of anti-Candida activity of three constituents of geranium oil is evaluated in this study. No fluconazole resistance was observed among the clinical isolates
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