218308
α-Pinene oxide
97%
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About This Item
Formula empirica (notazione di Hill):
C10H16O
Numero CAS:
Peso molecolare:
152.23
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
Livello qualitativo
Saggio
97%
Stato
liquid
Indice di rifrazione
n20/D 1.469 (lit.)
P. ebollizione
102-103 °C/50 mmHg (lit.)
Densità
0.964 g/mL at 25 °C (lit.)
Stringa SMILE
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
NQFUSWIGRKFAHK-BGPATTHWSA-N
Categorie correlate
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
150.8 °F - closed cup
Punto d’infiammabilità (°C)
66 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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I clienti hanno visto anche
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 218308-250G | |
| 218308-50G | 4061838775436 |
| 218308-5KG |
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