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218308

α-Pinene oxide

97%

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
1686-14-2
Molecular Weight:
152.23
NACRES:
NA.23
PubChem Substance ID:
24853058
UNSPSC Code:
12162002
EC Number:
216-869-6
MDL number:
MFCD00066955
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Quality Level

100

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

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

150.8 °F - closed cup

flash_point_c

66 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX9432
MKCW7904
MKCW5908
MKCS9313
MKCS1516

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H Zorn et al.
Journal of biotechnology, 107(3), 255-263 (2004-01-23)
When submerged cultured Pseudomonas fluorescens NCIMB 11761 was fed-batch supplemented with alpha-pinene oxide, a rapid formation of 2,6-dimethyl-5-methylene-hept-(2Z)-enal (I) (isonovalal) was observed. Biotransformation and isomerisation of (I) to the (2E)-isomer (II) (novalal) were enhanced by Lewatit OC 1064, a macroporous
Denis Linares et al.
Bioresource technology, 99(11), 4590-4596 (2007-09-15)
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
Series: 'Current issues in mutagenesis and carcinogenesis', No. 25.
P A Lefevre
Mutation research, 260(1), 5-7 (1991-05-01)
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Global Trade Item Number

SKUGTIN
218308-50G04061838775436