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About This Item
Empirical Formula (Hill Notation):
C8H14CaO10
CAS Number:
Molecular Weight:
310.27
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5166008
Product Name
L-Threonic acid hemicalcium salt, >97%
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
SMILES string
OC[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)CO
InChI key
ZJXGOFZGZFVRHK-BALCVSAKSA-L
assay
>97%
optical activity
[α]20/D +16°, c = 1 in H2O
mp
>300 °C (lit.)
Quality Level
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Application
Reactant involved in:
- Synthesis of cyclic hydroxamates and substituted oxazinanones
- Oxidative degradation to yield oxalate complexes
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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