Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C26H48O12 |
Molecular Weight | 552.6521 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCC(=O)OC[C@@]2(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)O[C@H](CO)[C@@H](O)[C@@H]2O
InChI
InChIKey=UEYVMVXJVDAGBB-ZHBLIPIOSA-N
InChI=1S/C26H48O12/c1-2-3-4-5-6-7-8-9-10-11-12-13-19(29)35-16-26(24(34)21(31)18(15-28)37-26)38-25-23(33)22(32)20(30)17(14-27)36-25/h17-18,20-25,27-28,30-34H,2-16H2,1H3/t17-,18-,20-,21-,22+,23-,24+,25-,26+/m1/s1
Molecular Formula | C26H48O12 |
Molecular Weight | 552.6521 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthetic long-chain alkyl maltosides and alkyl sucrose esters as enhancers of nasal insulin absorption. | 2002 Jun |
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PFGSE-NMR study of the self-diffusion of sucrose fatty acid monoesters in water. | 2005 Jun 1 |
|
Emulsification mechanism and storage instabilities of hydrocarbon-in-water sub-micron emulsions stabilised with Tweens (20 and 80), Brij 96v and sucrose monoesters. | 2009 Oct 1 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:09:56 GMT 2023
by
admin
on
Fri Dec 15 19:09:56 GMT 2023
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Record UNII |
P5KF9WAG4S
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Record Status |
Validated (UNII)
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Record Version |
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200615-17-4
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