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48798

Supelco

Geraniol

analytical standard

Sinônimo(s):

trans-3,7-Dimethyl-2,6-octadien-1-ol

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About This Item

Fórmula linear:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2OH
Número CAS:
106-24-1
Peso molecular:
154.25
Beilstein:
1722456
Número CE:
203-377-1
Número MDL:
MFCD00002917
Código UNSPSC:
85151701
ID de substância PubChem:
329757403
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

densidade de vapor

5.31 (vs air)

Ensaio

≥98.5% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.474 (lit.)
n20/D 1.478

pb

229-230 °C (lit.)

densidade

0.879 g/mL at 20 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

C\C(C)=C\CC\C(C)=C\CO

InChI

1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+

chave InChI

GLZPCOQZEFWAFX-JXMROGBWSA-N

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Aplicação

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

Outras notas

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

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H315,H317,H318

Classificações de perigo

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

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

226.4 °F - closed cup

Ponto de fulgor (°C)

108 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCK3343
BCCJ3456
BCCG9387
BCCF7485
BCCC0198

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Sigma-Aldrich

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Pankaj K Sharma et al.
Plant science : an international journal of experimental plant biology, 203-204, 63-73 (2013-02-19)
Plants synthesize volatile alcohol esters on environmental insult or as metabolic induction during flower/fruit development. However, essential oil plants constitutively produce them as the oil constituents. Their synthesis is catalyzed by BAHD family enzymes called alcohol acyltransferases (AATs). However, no
A Lapczynski et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S160-S170 (2008-07-22)
A toxicologic and dermatologic review of geraniol when used as a fragrance ingredient is presented.
Edita E Revay et al.
Acta tropica, 124(1), 102-105 (2012-07-04)
We conducted a study to determine the degree of personal protection provided by the Terminix(®) ALLCLEAR(®) Mosquito Mister - Lantern Edition. This outdoor unit was operated to disperse an aerosolized aqueous 0.3% geraniol emulsion in timed-release intervals of 5.0, 7.5
Lina Hagvall et al.
Contact dermatitis, 68(4), 224-231 (2013-03-21)
Geraniol is a commonly used fragrance terpene, and is tested in the baseline series in fragrance mix I. Geraniol is a pro-hapten and a pre-hapten, and sensitizers are formed in the autoxidation and skin metabolism of geraniol. Previous patch testing
Naoko Sato-Masumoto et al.
Phytochemistry, 104, 12-20 (2014-05-28)
Studies on the biosynthesis of oil compounds in Perilla will help in understanding regulatory systems of secondary metabolites and in elucidating reaction mechanisms for natural product synthesis. In this study, two types of alcohol dehydrogenases, an aldo-keto reductase (AKR) and
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