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About This Item
Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352201
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-174-1
Beilstein/REAXYS Number:
1723080
MDL number:
Quality Level
assay
≥99%
form
powder
optical activity
[α]24/D −18.7°, c = 4 in H2O
mp
150-152 °C (lit.)
SMILES string
O[C@H]1COC(O)[C@@H](O)[C@@H]1O
InChI
1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5+/m1/s1
InChI key
PYMYPHUHKUWMLA-WISUUJSJSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
涉药品监管产品
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Cyclopentyl methyl ether (CPME) was evaluated for extracting oil or triacylglycerol (TAG) from wet cells of the oleaginous yeast Lipomyces starkeyi. CPME is a greener alternative to chloroform as a potential solvent for oil recovery. A monophasic system of CPME
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Misun Lee et al.
Biotechnology for biofuels, 13, 5-5 (2020-01-16)
Efficient bioethanol production from hemicellulose feedstocks by Saccharomyces cerevisiae requires xylose utilization. Whereas S. cerevisiae does not metabolize xylose, engineered strains that express xylose isomerase can metabolize xylose by converting it to xylulose. For this, the type II xylose isomerase
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 851590-25G | 04061833023600 |
| 851590-5G | 04061833023617 |