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MFCD17215923 molecular structure
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sodium (2R)-2,3-dihydroxy-3-methylbutanoate hydrate

ChemBase ID: 154133
Molecular Formular: C5H11NaO5
Molecular Mass: 174.12761
Monoisotopic Mass: 174.05041773
SMILES and InChIs

SMILES:
CC(C)([C@H](C(=O)[O-])O)O.O.[Na+]
Canonical SMILES:
O[C@H](C(O)(C)C)C(=O)[O-].O.[Na+]
InChI:
InChI=1S/C5H10O4.Na.H2O/c1-5(2,9)3(6)4(7)8;;/h3,6,9H,1-2H3,(H,7,8);;1H2/q;+1;/p-1/t3-;;/m0../s1
InChIKey:
KGRRZNPTTZIUMS-QTNFYWBSSA-M

Cite this record

CBID:154133 http://www.chembase.cn/molecule-154133.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
sodium (2R)-2,3-dihydroxy-3-methylbutanoate hydrate
IUPAC Traditional name
sodium (R)-2,3-dihydroxy-isovalerate hydrate
Synonyms
(R)-2,3-Dihydroxy-3-methylbutanoic acid sodium salt
D(-)-α,β-Dihydroxyisovaleric acid sodium salt
(R)-Sodium 2,3-dihydroxyisovalerate hydrate
MDL Number
MFCD17215923
Beilstein Number
1722372
PubChem SID
162248272
PubChem CID
71311801

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
76455 external link Add to cart Please log in.
Data Source Data ID
PubChem 71311801 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 3.7976532  H Acceptors
H Donor LogD (pH = 5.5) -2.52605 
LogD (pH = 7.4) -4.0850472  Log P -0.8215878 
Molar Refractivity 40.2776 cm3 Polarizability 11.740738 Å3
Polar Surface Area 80.59 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/38 expand Show data source
Safety Statements
26 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319 expand Show data source
GHS Precautionary statements
P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
≥95.0% (CE) expand Show data source
Optical Purity
enantiomeric excess: ≥98.0% expand Show data source
Empirical Formula (Hill Notation)
C5H9O4Na · xH2O expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 76455 external link
Biochem/physiol Actions
Important metabolite of branched chain amino acid pathways.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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