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Dokumente

218308

Sigma-Aldrich

α-Pinenoxid

97%

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About This Item

Empirische Formel (Hill-System):
C10H16O
CAS-Nummer:
1686-14-2
Molekulargewicht:
152.23
EG-Nummer:
216-869-6
MDL-Nummer:
MFCD00066955
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24853058

Qualitätsniveau

100

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.469 (lit.)

bp

102-103 °C/50 mmHg (lit.)

Dichte

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

InChIKey

NQFUSWIGRKFAHK-BGPATTHWSA-N

Verwandte Kategorien

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

150.8 °F - closed cup

Flammpunkt (°C)

66 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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(1R,2R,3S,5R)-(−)-Pinandiol 99%

Sigma-Aldrich

287784

(1R,2R,3S,5R)-(−)-Pinandiol

(−)-Carveol, Isomerengemisch 97%

Sigma-Aldrich

192384

(−)-Carveol, Isomerengemisch

(±)-exo,exo-2,3-Camphanediol 97%

Sigma-Aldrich

658731

(±)-exo,exo-2,3-Camphanediol

(−)-β-Pinen ≥99%

Sigma-Aldrich

402753

(−)-β-Pinen

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
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
A Boontawan et al.
Applied microbiology and biotechnology, 69(6), 643-649 (2005-08-10)
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
Apichat Boontawan et al.
Biotechnology progress, 21(6), 1680-1687 (2005-12-03)
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
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
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