380644
L-Threonic acid hemicalcium salt
>97%
Synonym(s):
(2R,3S)-2,3,4-Trihydroxybutyric acid hemicalcium salt, L-Threonic acid calcium salt
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About This Item
Empirical Formula (Hill Notation):
C8H14CaO10
CAS Number:
Molecular Weight:
310.27
Beilstein:
5166008
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
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Assay
>97%
optical activity
[α]20/D +16°, c = 1 in H2O
mp
>300 °C (lit.)
SMILES string
OC[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)CO
InChI
1S/2C4H8O5.Ca/c2*5-1-2(6)3(7)4(8)9;/h2*2-3,5-7H,1H2,(H,8,9);/q;;+2/p-2/t2*2-,3+;/m00./s1
InChI key
ZJXGOFZGZFVRHK-BALCVSAKSA-L
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Application
Reactant involved in:
- Synthesis of cyclic hydroxamates and substituted oxazinanones
- Oxidative degradation to yield oxalate complexes
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
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Ya-Ting Lin et al.
Chemosphere, 136, 27-31 (2015-04-29)
Alkaline ascorbic acid (AA) was recently discovered as a novel in-situ chemical reduction (ISCR) reagent for remediating chlorinated solvents in the subsurface. For this ISCR process, the maintenance of an alkaline pH is essential. This study investigated the possibility of
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