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(R)-Mevalonic acid lithium salt_Molecular_structure_CAS_)
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(R)-Mevalonic acid lithium salt

Catalog No. 50838 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C6H11LiO4 Telephone 1-800-521-8956
M. W. 154.09014 Fax
Purity ≥93.0% (qNMR) Email
Storage Chembase ID: 154631

SYNONYMS

IUPAC name
lithium(1+) ion (3R)-3,5-dihydroxy-3-methylpentanoate
IUPAC Traditional name
lithium(1+) ion (R)-mevalonate
Synonyms
Lithium (R)-3,5-dihydroxy-3-methylvalerate
Lithium (R)-3,5-dihydroxy-3-methylpentanoate

DATABASE IDS

MDL Number MFCD18632545

PROPERTIES

Empirical Formula (Hill Notation) C6H11LiO4
Purity ≥93.0% (qNMR)
Optical Rotation [α]/D -22.0±3.0°, c = 0.1 in 1 M HCl (3 h)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H319
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
GHS Precautionary statements P305 + P351 + P338
Risk Statements 22-36
Safety Statements 26
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (简体中文)
Biochem/physiol Actions
Mevalonic acid1,2, is an intermediate in the mevalonate pathway, producing terpenes and steroids. This function provides treatment options metabolic disorders3,4,5,6,7,8, R-mevalonate accumulates in patients with the autosomal recessively inherited mevalonic acidurias, an inborn error of cholesterol and nonsterol isoprene biosynthesis9.
Description (English)
Biochem/physiol Actions
Mevalonic acid1,2, is an intermediate in the mevalonate pathway, producing terpenes and steroids. This function provides treatment options metabolic disorders3,4,5,6,7,8, R-mevalonate accumulates in patients with the autosomal recessively inherited mevalonic acidurias, an inborn error of cholesterol and nonsterol isoprene biosynthesis9.

REFERENCES