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218308

Sigma-Aldrich

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
EC Number:
216-869-6
MDL number:
MFCD00066955
UNSPSC Code:
12162002
PubChem Substance ID:
24853058
NACRES:
NA.23

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 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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Certificates of Analysis (COA)

Lot/Batch Number
MKCW7904
MKCW5908
MKCS9313
MKCS1516
MKCR3991

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Series: 'Current issues in mutagenesis and carcinogenesis', No. 25.
P A Lefevre
Mutation research, 260(1), 5-7 (1991-05-01)
Hendrik Schewe et al.
Applied microbiology and biotechnology, 78(1), 55-65 (2007-12-07)
Escherichia coli BL21, expressing a quintuple mutant of P450(BM-3), oxyfunctionalizes alpha-pinene in an NADPH-dependent reaction to alpha-pinene oxide, verbenol, and myrtenol. We optimized the whole-cell biocatalyst by integrating a recombinant intracellular NADPH regeneration system through co-expression of a glucose facilitator
Mass spectrometric studies of DNA adducts from a reaction with terpenoids.
Wolfgang Schrader et al.
Angewandte Chemie (International ed. in English), 43(48), 6657-6660 (2004-12-14)
E T Griffiths et al.
Journal of bacteriology, 169(11), 4972-4979 (1987-11-01)
Over 20 gram-positive bacteria were isolated by elective culture with (+/-)-alpha-pinene as the sole carbon source. One of these strains, Nocardia sp. strain P18.3, was selected for detailed study. alpha-Pinene-grown cells oxidized, without lag, alpha-pinene, alpha-pinene oxide (epoxide), and the
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
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