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About This Item
Empirical Formula (Hill Notation):
C10H16O
CAS Number:
Molecular Weight:
152.23
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
Assay
97%
form
liquid
refractive index
n20/D 1.469 (lit.)
bp
102-103 °C/50 mmHg (lit.)
density
0.964 g/mL at 25 °C (lit.)
SMILES string
CC1(C)[C@H]2CC3OC3(C)[C@@H]1C2
InChI
1S/C10H16O/c1-9(2)6-4-7(9)10(3)8(5-6)11-10/h6-8H,4-5H2,1-3H3/t6-,7-,8?,10?/m1/s1
InChI key
NQFUSWIGRKFAHK-BGPATTHWSA-N
Related Categories
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The feasibility of trans-2-methyl-5-isopropylhexa-2,5-dienoic acid (novalic acid) accumulation using the alpha-pinene degradation pathway of Pseudomonas rhodesiae CIP 107491 was studied. This appeared possible by using concentrated living bacterial cells produced under oxygen limitation with alpha-pinene as sole carbon source. The
H Zorn et al.
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P Fontanille et al.
Applied microbiology and biotechnology, 60(5), 534-540 (2003-01-22)
Optimization studies on the synthesis of isonovalal from alpha-pinene oxide by Pseudomonas rhodesiae CIP 107491 operated in a biphasic medium are presented. Three key parameters are identified. The first is the need for a permeabilization of cells by freezing them
A Boontawan et al.
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In this work the biotransformation of alpha-pinene oxide to isonovalal using resting cells of Pseudomonas fluorescens NCIMB 11671 was evaluated in a membrane bioreactor for biotransformations (MBB). Since the membrane area required to obtain optimum productivities was calculated to be
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Terpenoids are important compounds for the fragrance industry, and recently, biocatalytic methods have been developed to produce them from cheap monoterpenes, such as alpha-pinene oxide. The biotransformation of alpha-pinene oxide using resting cells of Pseudomonas fluorescens NCIMB 11671 produces isonovalal
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