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85541

Sigma-Aldrich

L-(−)-Sorbose

for biotechnological purposes, ≥98.0% (sum of enantiomers, HPLC)

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About This Item

Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
87-79-6
Molecular Weight:
180.16
Beilstein:
1724554
EC Number:
201-771-8
MDL number:
MFCD00151097
UNSPSC Code:
12352201
PubChem Substance ID:
57653051
NACRES:
NA.25

grade

for biotechnological purposes

Assay

≥98.0% (sum of enantiomers, HPLC)

form

solid

optical activity

[α]20/D −43±2°, c = 5% in H2O

color

colorless

mp

163-165 °C

solubility

H2O: 0.1 g/mL, clear, colorless to very faintly yellow

SMILES string

OC[C@H](O)[C@@H](O)[C@H](O)C(=O)CO

InChI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5+,6+/m0/s1

InChI key

BJHIKXHVCXFQLS-OTWZMJIISA-N

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Application

L-Sorbose is used as a starting reagent for the commercial biosynthesis of ascorbic acid (vitamin C).

Biochem/physiol Actions

The L enatiomer of sorbose, a ketohexose monosaccharide.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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