Substance

ID:349956

Names and Identifiers
IUPAC name
(2R,3S)-butane-1,2,3,4-tetrol
IUPAC Traditional name
erythritol
Synonyms
meso-Erythritol1,2,3,4-Butanetetrolmeso-1,2,3,4-Tetrahydroxybutanei-Erythritol
Registration numbers
CAS Number
PubChem SID
Beilstein Number
MDL Number
EC Number
Properties
Safety Information
MSDS Link
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Storage Temperature
-20°C
RTECS
KF2000000
German water hazard class
3
Physical Property
Sweetness
0.7 × sucrose
Melting Point
118-120 °C(lit.)
Boiling Point
329-331 °C(lit.)
Product Information
Linear Formula
HOCH2[CH(OH)]2CH2OH
Purity
≥99%
Molecule Details
Biochem/physiol Actions
Allelic variation of the Tas1r3 gene affects behavioral taste responses to this sugar alcohol, suggesting that it is a T1R3 receptor ligand.1
Packaging
25, 100 g in poly bottle
Application
Meso-Erythritol is a precursor to the important tanning agent L-erythrulose which can be commercially generated by Gluconobacter oxydans DSM 7145. Meso-Erythritol, an aliphatic poly-alcohol, is used in the chemical analysis of the reativity of various radicals and radical anions.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. E7500.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Molecular Spectra
No Data Available
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References
No Data Available
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