192384
(-)-香芹醇，异构体混合物
97%
别名:
葛缕醇
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经验公式（希尔记法）:
C10H16O
化学文摘社编号:
分子量:
152.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
EC Number:
202-757-4
MDL number:
Assay:
97%
InChI key
BAVONGHXFVOKBV-YHMJZVADSA-N
InChI
1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10?/m1/s1
SMILES string
CC(=C)[C@@H]1CC=C(C)C(O)C1
assay
97%
optical activity
[α]20/D −112°, c = 1 in chloroform
refractive index
n20/D 1.496 (lit.)
bp
226-227 °C/751 mmHg (lit.)
density
0.958 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Imran Malik et al.
Frontiers in neuroscience, 14, 659-659 (2020-07-28)
Ischemic stroke is a severe neurological disorder with a high prevalence rate in developed countries. It is characterized by permanent or transient cerebral ischemia and it activates syndrome of pathological events such as membrane depolarization, glutamate excitotoxicity, and intracellular calcium
Jenna L E Morrish et al.
Biotechnology and bioengineering, 101(4), 768-775 (2008-05-15)
The microbial biotransformation of (-)-trans-carveol to the flavor and fragrance compound (R)-(-)-carvone by Rhodococcus erythropolis DCL14 was carried out in a 3 L two phase partitioning bioreactor with an immiscible liquid second phase in an effort to improve upon the
Jenna L E Morrish et al.
Biotechnology letters, 30(7), 1245-1250 (2008-03-11)
The aqueous substrate and product toxicity thresholds in the microbial biotransformation of (-)-trans-carveol to the fragrance/flavor compound (R)-(-)-carvone by Rhodococcus erythropolis were determined. Above aqueous phase concentrations of approx. 500 mg carveol/l and 200-600 mg carvone/l, the biotransformation activity of
M Wüst et al.
Archives of biochemistry and biophysics, 387(1), 125-136 (2001-05-23)
Limonene enantiomers and substrate analogs, including specifically fluorinated derivatives, were utilized to probe active site interactions with recombinant (-)-(4S)-limonene-3-hydroxylase (CYP71D13) and (-)-(4S)-limonene-6-hydroxylase (CYP71D18) from mint (Mentha) species. (-)-(4S)-Limonene is hydroxylated by both enzymes at the designated C3- and C6-allylic positions
Biotransformation of D-limonene to (+) trans-carveol by toluene-grown Rhodococcus opacus PWD4 cells.
W A Duetz et al.
Applied and environmental microbiology, 67(6), 2829-2832 (2001-05-26)
The toluene-degrading strain Rhodococcus opacus PWD4 was found to hydroxylate D-limonene exclusively in the 6-position, yielding enantiomerically pure (+) trans-carveol and traces of (+) carvone. This biotransformation was studied using cells cultivated in chemostat culture with toluene as a carbon
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