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C1049

Sigma-Aldrich

(+)-Calcium L-tartrate hydrate

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About This Item

Empirical Formula (Hill Notation):
C4H4O6Ca · xH2O
CAS Number:
Molecular Weight:
188.15 (anhydrous basis)
EC Number:
UNSPSC Code:
12352200
PubChem Substance ID:

SMILES string

O[C@@H]1[C@@H](O)C(=O)O[Ca]OC1=O

InChI

1S/C4H6O6.Ca/c5-1(3(7)8)2(6)4(9)10;/h1-2,5-6H,(H,7,8)(H,9,10);/q;+2/p-2/t1-,2-;/m1./s1

InChI key

GUPPESBEIQALOS-ZVGUSBNCSA-L

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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J B Olivato et al.
Carbohydrate polymers, 92(2), 1705-1710 (2013-02-13)
Tartaric acid (TA), a dicarboxylic acid, can act as a compatibiliser in starch/polyester blends. A mixture design was proposed to evaluate the effect of TA on the properties of starch/poly (butylene adipate co-terephthalate) (PBAT) blown films plasticised with glycerol. The
Mark D Eddleston et al.
Chemical communications (Cambridge, England), 48(92), 11340-11342 (2012-10-18)
The formation of diastereomeric cocrystals of malic acid and tartaric acid was investigated by liquid-assisted grinding in the solid state. We demonstrate that racemic malic acid can be converted into two distinct diastereomeric cocrystal phases by grinding with a single
M Suman et al.
Die Pharmazie, 67(8), 687-694 (2012-09-11)
Asymmetric membrane capsules (AMCs) are based on the concept of osmotic pressure but are much simpler to manufacture. Further, they can be suitably optimized by varying the parameters like concentration of pore former, polymer, osmotic agents and solubility enhancers to
Ling-li Lu et al.
Journal of Zhejiang University. Science. B, 14(2), 106-114 (2013-02-01)
The elucidation of a natural strategy for metal hyperaccumulation enables the rational design of technologies for the clean-up of metal-contaminated soils. Organic acid has been suggested to be involved in toxic metallic element tolerance, translocation, and accumulation in plants. The
Gergely Varga et al.
Bioorganic & medicinal chemistry letters, 23(6), 1789-1792 (2013-02-12)
Di-O-cinnamoylated, -p-coumaroylated, and -feruloylated d-, l- and meso-tartaric acids were synthesized as analogues of the natural product FR258900, a glycogen phosphorylase (GP) inhibitor with in vivo antihyperglycaemic activity. The new compounds inhibited rabbit muscle GP in the low micromolar range

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