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About This Item
Empirical Formula (Hill Notation):
C22H40O12
CAS Number:
Molecular Weight:
496.55
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
250-828-3
Beilstein/REAXYS Number:
4924317
MDL number:
InChI key
STVGXWVWPOLILC-LUQRLMJOSA-N
InChI
1S/C22H40O12/c1-2-3-4-5-6-7-8-9-15(25)31-11-14-16(26)18(28)19(29)21(32-14)34-22(12-24)20(30)17(27)13(10-23)33-22/h13-14,16-21,23-24,26-30H,2-12H2,1H3/t13-,14-,16-,17-,18+,19-,20+,21-,22+/m1/s1
SMILES string
CCCCCCCCCC(=O)OC[C@H]1O[C@H](O[C@]2(CO)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
description
non-ionic
mol wt
496.55 g/mol
CMC
2.5
storage temp.
−20°C
Quality Level
Related Categories
Analysis Note
Mixture of esters
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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Pranee Inprakhon et al.
Journal of biotechnology, 259, 182-190 (2017-07-29)
Sucrose monocaprate was synthesized by carrying out a lipase-catalyzed transesterification in a non-aqueous biphasic medium. Vinyl caprate was mechanically dispersed into a solution of sucrose in DMSO. The use of DMSO allowed increasing sucrose concentration up to 0.7M (in DMSO).
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