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48798

Supelco

Geraniol

analytical standard

Sinónimos:

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

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About This Item

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

grado

analytical standard

Nivel de calidad

100

densidad de vapor

5.31 (vs air)

Análisis

≥98.5% (GC)

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

índice de refracción

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

bp

229-230 °C (lit.)

densidad

0.879 g/mL at 20 °C (lit.)

aplicaciones

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

formato

neat

temp. de almacenamiento

2-8°C

cadena 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+

Clave InChI

GLZPCOQZEFWAFX-JXMROGBWSA-N

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Aplicación

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

Otras notas

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

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palabra de señalización

Danger

Frases de peligro

H315,H317,H318

Clasificaciones de peligro

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

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

226.4 °F - closed cup

Punto de inflamabilidad (°C)

108 °C - closed cup

Equipo de protección personal

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

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCK3343
BCCJ3456
BCCG9387
BCCF7485
BCCC0198

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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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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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