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Merck

289140

Cadmium carbonate

powder, 98%

Synonym(s):

Otavite

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About This Item

Linear Formula:
CdCO3
CAS Number:
513-78-0
Molecular Weight:
172.42
NACRES:
NA.23
PubChem Substance ID:
24857389
UNSPSC Code:
12352302
EC Number:
208-168-9
MDL number:
MFCD00010918
Assay:
98%
Form:
powder
Solubility:
H2O: insoluble(lit.)
aqueous acid: slightly soluble(lit.)

Key Documents

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Product Name

Cadmium carbonate, powder, 98%

InChI key

GKDXQAKPHKQZSC-UHFFFAOYSA-L

InChI

1S/CH2O3.Cd/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2

SMILES string

[Cd++].[O-]C([O-])=O

assay

98%

form

powder

reaction suitability

core: cadmium
reagent type: catalyst

mp

500 °C (lit.)

solubility

H2O: insoluble(lit.)
aqueous acid: slightly soluble(lit.)

density

4.258 g/mL at 25 °C (lit.)

Quality Level

200

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Related Categories

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Muta. 1B - Repr. 2 - STOT RE 1

target_organs

Lungs,Kidney,Bone

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX5664
MKCM7519
MKCF3343
MKBW4510V
MKBF5367V

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[Micromethod for the determination of polymorphonuclear granulocyte phagocytic ability using cadmium carbonate crystals].
U Thielebeule et al.
Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete, 29(2), 69-70 (1983-02-01)
T Niwa et al.
Steroids, 57(11), 522-529 (1992-11-01)
3-N-Acetylglucosaminides of unconjugated, glycine- and taurine-conjugated bile acids have been synthesized. Bile acids appropriately protected were condensed with acetochloroglucosamine through the 3 alpha-hydroxyl group by means of the Koenigs-Knorr reaction using cadmium carbonate as a catalyst. Subsequent borohydride reduction and/or
Zdenek Wimmer et al.
Bioorganic & medicinal chemistry, 15(22), 7126-7137 (2007-09-11)
A series of the protected alkyl glycosides 5a/5b-12a/12b was synthesized from the parent isomeric alcohols (insect juvenile hormone bioanalogs; juvenoids), 4-[4'-(2''-hydroxycyclohexyl)methylphenoxy]-3-methyl-but-2-enoic acid ethyl ester (1a/1b-4a/4b; racemic structures) and (1a-4a; enantiopure structures). Cadmium carbonate was used as a promoter of this
V Vĕtvicka et al.
Folia biologica, 31(1), 20-33 (1985-01-01)
In the high-responder A/J mice a lower percentage of peritoneal macrophages express Fc receptors and accordingly phagocytize less intensely via these receptors than the macrophages of the low-IgG-responder C57BL/10ScSn strain. Similarly, the phagocytosis mediated by the receptors for foreign substances
E Suzuki et al.
Steroids, 60(3), 277-284 (1995-03-01)
The synthesis of 15-N-acetylglucosaminides of 15 alpha-hydroxyesterone, 15 alpha-hydroxyestradiol, and 15 alpha-hydroxyestriol (estetrol) is described. The latter two were prepared by condensation of 2-acetamido-1 alpha-chloro-1,2-dideoxy-3,4,6-trio-O-acetyl-D-glucopyranose with appropriately protected 15 alpha-hydroxyestrogens by the Koenigs-Knorr reaction employing cadmium carbonate as a catalyst.
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