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Sigma-Aldrich

(R)-(−)-3-Hydroxybutyric acid sodium salt

optical purity ee: 99% (GLC)

Synonym(s):

Sodium (R)-3-hydroxybutyrate

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About This Item

Linear Formula:
CH3CH(OH)CH2CO2Na
CAS Number:
13613-65-5
Molecular Weight:
126.09
Beilstein:
6118796
MDL number:
MFCD00077788
UNSPSC Code:
12352001
PubChem Substance ID:
24857981
NACRES:
NA.22

form

solid

optical activity

[α]22/D −14°, c = 10 in H2O

optical purity

ee: 99% (GLC)

mp

149-155 °C (lit.)

SMILES string

[Na+].C[C@@H](O)CC([O-])=O

InChI

1S/C4H8O3.Na/c1-3(5)2-4(6)7;/h3,5H,2H2,1H3,(H,6,7);/q;+1/p-1/t3-;/m1./s1

InChI key

NBPUSGBJDWCHKC-AENDTGMFSA-M

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Application

(R)-(-)-3-Hydroxybutyric acid sodium salt reacts with crown ether to form a supramolecular complex, which can catalyze the regioselective ring-opening polymerization of (S)-butyrolactone to form (R)-3-hydroxybutyrate oligomers (OHBs).

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)

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Gokel GW
Advances in Supramolecular Chemistry, 7, 61-61 (2001)
Joel S Benjamin et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(1), 125-130 (2016-12-22)
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Sabrina Chriett et al.
Scientific reports, 9(1), 742-742 (2019-01-27)
Butyrate and R-β-hydroxybutyrate are two related short chain fatty acids naturally found in mammals. Butyrate, produced by enteric butyric bacteria, is present at millimolar concentrations in the gastrointestinal tract and at lower levels in blood; R-β-hydroxybutyrate, the main ketone body

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