Skip to Content
MilliporeSigma
All Photos(1)

Documents

196428

Sigma-Aldrich

Dihydromyrcenol

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Looking for similar products? Visit Product Comparison Guide

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

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service