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S1266

Sigma-Aldrich

Sucrose monodecanoate

Synonym(s):

Capric acid sucrose ester, Sucrose monocaprate, n-Decanoylsucrose

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About This Item

Empirical Formula (Hill Notation):
C22H40O12
CAS Number:
Molecular Weight:
496.55
Beilstein/REAXYS Number:
4924317
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

description

non-ionic

Quality Level

mol wt

496.55 g/mol

CMC

2.5

storage temp.

−20°C

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

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

InChI key

STVGXWVWPOLILC-LUQRLMJOSA-N

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Quality

Mixture of esters

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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