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72638

Supelco

(±)-Citronellal

analytical standard

Synonyme(s) :

(±)-3,7-Dimethyl-6-octenal

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About This Item

Formule linéaire :
(CH3)2C=CHCH2CH2CH(CH3)CH2CHO
Numéro CAS:
106-23-0
Poids moléculaire :
154.25
Numéro Beilstein :
1720789
Numéro CE :
203-376-6
Numéro MDL:
MFCD00038090
Code UNSPSC :
85151701
ID de substance PubChem :
329764230
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥95.0% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.451 (lit.)

Point d'ébullition

207 °C (lit.)

Densité

0.857 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CC(CC\C=C(\C)C)CC=O

InChI

1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,8,10H,4,6-7H2,1-3H3

Clé InChI

NEHNMFOYXAPHSD-UHFFFAOYSA-N

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Application

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

Autres remarques

This compound is commonly found in plants of the genus: melissa

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H317,H319

Classification des risques

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

165.2 °F - closed cup

Point d'éclair (°C)

74 °C - closed cup

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCK2761
BCCK5032
BCCG3305
BCCF0602
BCCC8988

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Sigma-Aldrich

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Sigma-Aldrich

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Citronellol

Yathsoeung Ho et al.
Pharmaceuticals (Basel, Switzerland), 13(12) (2020-12-24)
Triple negative breast cancer is one of the most aggressive breast cancer type with abilities of early metastasis and chemoresistance. The tropical plant Citrus hystrix DC. has been reported to promote many biological activities including anticancer. However, the effect of
Walter S Leal et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(46), 18704-18709 (2013-10-30)
The southern house mosquito, Culex quinquefasciatus, has one of the most acute and eclectic olfactory systems of all mosquito species hitherto studied. Here, we used Illumina sequencing to identify olfactory genes expressed predominantly in antenna, mosquito's main olfactory organ. Less
Alina Mariana Balu et al.
Organic & biomolecular chemistry, 8(12), 2845-2849 (2010-05-01)
The selective conversion of citronellal to menthols, with good diastereoselectivities to (-)-menthol for the case of (+)-citronellal as starting material, can effectively be carried out in a one-step reaction under microwave irradiation catalysed by supported nanoparticles on mesoporous materials. 2%
Gabriele Siedenburg et al.
Applied and environmental microbiology, 78(4), 1055-1062 (2011-12-14)
The biosynthesis of cyclic monoterpenes (C(10)) generally requires the cyclization of an activated linear precursor (geranyldiphosphate) by specific terpene cyclases. Cyclic triterpenes (C(30)), on the other hand, originate from the linear precursor squalene by the action of squalene-hopene cyclases (SHCs)
M S Melo et al.
Pharmaceutical biology, 48(4), 411-416 (2010-07-22)
Citronellal is a monoterpene reported to be a major component of the essential oils in various aromatic species of plants. The present study evaluated the central nervous system depressant and antinociceptive properties of citronellal through behavioral experimental models. Following intraperitoneal
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