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252603

Sigma-Aldrich

D-(+)-Sucrose octaacetate

98%

Synonym(s):

Octa-O-acetylsucrose, SOA, Sucrose octaacetate

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About This Item

Empirical Formula (Hill Notation):
C28H38O19
CAS Number:
Molecular Weight:
678.59
Beilstein:
79290
EC Number:
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

powder

optical activity

[α]22/D +58.8°, c = 2.5 in ethanol

bp

260 °C (lit.)

mp

82-85 °C (lit.)

SMILES string

CC(=O)OC[C@H]1O[C@H](O[C@]2(COC(C)=O)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

1S/C28H38O19/c1-12(29)37-9-20-22(40-15(4)32)24(42-17(6)34)25(43-18(7)35)27(45-20)47-28(11-39-14(3)31)26(44-19(8)36)23(41-16(5)33)21(46-28)10-38-13(2)30/h20-27H,9-11H2,1-8H3/t20-,21-,22-,23-,24+,25-,26+,27-,28+/m1/s1

InChI key

ZIJKGAXBCRWEOL-SAXBRCJISA-N

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Application

Sucrose octaacetate (SOA) is a bitter-tasting acetylated sugar that is commonly used to study gustatory sensitivity in mice.
  • SOA can undergo partial deacetylation by lipases or proteases to form analogs, which are useful intermediates for synthesizing artificial sweeteners.
  • It can also be used as an in situ seed and a soft template to synthesize polyaniline (PANI) nanofibers under acidic conditions by the oxidative polymerization of aniline using ammonium peroxydisulfate (APS) as an oxidizing agent.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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{Human taste thresholds for sucrose octaacetate.
Boughter Jr J D and Whitney G
Chemical Senses, 18(4), 445-448 (1993)
Sucrose octaacetate-taster mice have more vallate taste buds than non-tasters .
Miller Jr I J and Whitney G
Neuroscience Letters, 100(1-3) (1989)
Sucrose octaacetate tasting in a heterogeneous population of CFW mice.
Gannon K S and Whitney G
Behavior Genetics, 19(3), 417-431 (1989)
Synthesis of polyaniline nanostructures via soft template of sucrose octaacetate.
Qiu H, et al.
Synt. Metals, 160(11-12), 1179-1183 (2010)
Regioselective enzymatic deacetylation of sucrose octaacetate in organic solvents.
Palmer D C and Terradas F
Tetrahedron Letters, 35(11), 1673-1676 (1994)

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