196428
Dihydromyrcenol
99%
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About This Item
Linear Formula:
H2C=CHCH(CH3)(CH2)3C(CH3)2OH
CAS Number:
Molecular Weight:
156.27
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
242-362-4
MDL number:
InChI key
XSNQECSCDATQEL-UHFFFAOYSA-N
InChI
1S/C10H20O/c1-5-9(2)7-6-8-10(3,4)11/h5,9,11H,1,6-8H2,2-4H3
SMILES string
CC(CCCC(C)(C)O)C=C
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.)
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
168.8 °F - closed cup
flash_point_c
76 °C - closed cup
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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)
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
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
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