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C83201

Sigma-Aldrich

β-Citronellol

95%

Sinonimo/i:

(±)-β-Citronellol, beta-Citronellol, 3,7-Dimethyl-6-octen-1-ol

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About This Item

Formula condensata:
(CH3)2C=CHCH2CH2CH(CH3)CH2CH2OH
Numero CAS:
106-22-9
Peso molecolare:
156.27
Beilstein:
1721507
Numero CE:
203-375-0
Numero MDL:
MFCD00002935
Codice UNSPSC:
12352100
ID PubChem:
24893050
NACRES:
NA.22

Densità del vapore

5.4 (vs air)

Tensione di vapore

~0.02 mmHg ( 25 °C)

Saggio

95%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.456 (lit.)

P. eboll.

222 °C (lit.)

Densità

0.857 g/mL at 25 °C (lit.)

Stringa SMILE

CC(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
QMVPMAAFGQKVCJ-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H317,H319

Classi di pericolo

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

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

224.6 °F - closed cup

Punto d’infiammabilità (°C)

107 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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(±)-Citronellal analytical standard

Supelco

72638

(±)-Citronellal

Citronellol solution certified reference material, 2000 μg/mL in methanol, ampule of 1 mL

Supelco

CRM40469

Citronellol solution

Geraniol analytical standard

Supelco

48798

Geraniol

Citronellyl acetate ≥95%, FCC, FG

Sigma-Aldrich

W231118

Citronellyl acetate

(S)-(−)-Citronellal 96%

Sigma-Aldrich

373753

(S)-(−)-Citronellal

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
Wantida Chaiyana et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 19(8-9), 836-839 (2012-04-19)
Inhibition of cholinesterase has attracted much attention recently because of its potential for the treatment of Alzheimer's disease. In this work, the anticholinesterase activities of plant oils were investigated using Ellman's colorimetric method. The results indicate that essential oils obtained
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
Renan G Brito et al.
Basic & clinical pharmacology & toxicology, 112(4), 215-221 (2012-10-06)
Citronellol (CT) is a monoterpenoid alcohol present in the essential oil of many medicinal plants, such as Cymbopogon citratus. We evaluated the antinociceptive effects of CT on orofacial nociception in mice and investigated the central pathway involved in the effect.
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