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About This Item
Linear Formula:
(CH3)2CH(CH2)3CH(CH3)CH2CH2OH
CAS Number:
Molecular Weight:
158.28
EC Number:
203-374-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1719638
MDL number:
vapor density
5.4 (vs air)
vapor pressure
<0.01 mmHg ( 20 °C)
grade
purum
assay
≥98.0% (GC)
refractive index
n20/D 1.435, n20/D 1.436 (lit.)
bp
98-99 °C/9 mmHg (lit.)
density
0.828 g/mL at 20 °C (lit.)
SMILES string
CC(C)CCCC(C)CCO
InChI
1S/C10H22O/c1-9(2)5-4-6-10(3)7-8-11/h9-11H,4-8H2,1-3H3
InChI key
PRNCMAKCNVRZFX-UHFFFAOYSA-N
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
206.6 °F - closed cup
flash_point_c
97 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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J Pevsner et al.
The Journal of biological chemistry, 265(11), 6118-6125 (1990-04-15)
We have characterized the odorant binding properties of purified bovine odorant-binding protein (OBP) using as a ligand [3H]3,7-dimethyloctan-1-ol ([3H]DMO). A broad variety of odorants, including terpenes, aldehydes, esters, and musks, bind to OBP with affinities of 0.2 to 100 microM.
A Lapczynski et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S139-S141 (2008-07-22)
A toxicologic and dermatologic review of 3,7-dimethyl-1-octanol when used as a fragrance ingredient is presented.
Gul Majid Khan et al.
Pakistan journal of pharmaceutical sciences, 24(4), 451-457 (2011-10-01)
In the present study a new alcohol derivative of tetrahydrogeraniol (THG), an acyclic monoterpene, has been prepared by using Grignard reagent and methyl cyclopropyl ketone. Penetration enhancing effects of THG and the synthesized derivative 5,9-dimethyl-2-cyclopropyl-2-decanol (DICNOL) on the transdermal penetration
R M Hanif et al.
Chemical & pharmaceutical bulletin, 46(9), 1428-1431 (1998-10-17)
The tetrahydrogeraniol (THG) derivative, ethyl-(3,7-dimethyl octyl thio) acetate (EDOTA) was prepared by reacting tetrahydrogeranyl bromide (obtained by reaction of 40% hydrobromic acid and concentrated sulfuric acid) with ethyl 2-mercaptoacetate, while 3,7-dimethyl octyl propionate (DOP) was synthesized by a common esterification
Mineo Ikematsu et al.
Biochemical and biophysical research communications, 333(4), 1227-1233 (2005-06-28)
Why bovine odorant-binding protein (OBPb), among OBP family, assumes a dimeric structure has been unclear. Here we clarified, by measuring the fluorescence of intrinsic tryptophan and tyrosine residues of intact OBPb and OBPb whose C-terminal 10 amino acids were deleted
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