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196428

Sigma-Aldrich

Dihydromyrcenol

99%

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About This Item

Linear Formula:
H2C=CHCH(CH3)(CH2)3C(CH3)2OH
CAS Number:
18479-58-8
Molecular Weight:
156.27
EC Number:
242-362-4
MDL number:
MFCD00004474
UNSPSC Code:
12352100
PubChem Substance ID:
24851758

Assay

99%

form

liquid

refractive index

n20/D 1.443 (lit.)

bp

84 °C/10 mmHg (lit.)

density

0.837 g/mL at 20 °C
0.784 g/mL at 25 °C (lit.)

SMILES string

CC(CCCC(C)(C)O)C=C

InChI

1S/C10H20O/c1-5-9(2)7-6-8-10(3,4)11/h5,9,11H,1,6-8H2,2-4H3

InChI key

XSNQECSCDATQEL-UHFFFAOYSA-N

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General description

Methoxycarbonylation of dihydromyrcenol catalyzed by [PdCl2(PPh3)2]-SnCl2·2H2O-2PPh3 has been investigated. Dihydromyrcenol is a widely used fragrance ingredient and has been evaluated for developmental toxicity in pregnant Sprague-Dawley rats.

Application

Dihydromyrcenol was used in the synthesis of bioamphiphilic polymers based on the hydrophilic dextran and the hydrophobic terpenes as renewable resources.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup

Certificates of Analysis (COA)

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Dihydromyrcenol carbonylation catalyzed by palladium-tin precursors: selectivity of the reaction drawn by the experimental conditions and the co-reactants.
Lenoble G, et al.
Journal of Organometallic Chemistry, 643, 12-18 (2002)
Marie-Hélène Alvès et al.
Biomacromolecules, 15(1), 242-251 (2013-11-26)
The present work shows the synthesis of amphiphilic polymers based on the hydrophilic dextran and the hydrophobic terpenes as renewable resources. The first step concerns the synthesis of functional terpene molecules by thiol-ene addition chemistry involving amino or carboxylic acid
Valerie T Politano et al.
International journal of toxicology, 28(2), 80-87 (2009-06-02)
Dihydromyrcenol, a widely used fragrance ingredient, was evaluated for developmental toxicity in pregnant Sprague-Dawley rats (25/group). Oral dosages of 0, 250, 500, or 1000 mg/kg/d in corn oil were administered on gestational days 7 to 17. Rats were observed for

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