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Chemistry

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Also known as: 598-62-9, Manganese(ii) carbonate, Manganous carbonate, Rhodochrosite, Manganese carbonate (1:1), Carbonic acid, manganese salt
Molecular Formula
CMnO3
Molecular Weight
114.947  g/mol
InChI Key
XMWCXZJXESXBBY-UHFFFAOYSA-L
FDA UNII
9ZV57512ZM

Manganese Carbonate
1 2D Structure

Manganese Carbonate

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
manganese(2+);carbonate
2.1.2 InChI
InChI=1S/CH2O3.Mn/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2
2.1.3 InChI Key
XMWCXZJXESXBBY-UHFFFAOYSA-L
2.1.4 Canonical SMILES
C(=O)([O-])[O-].[Mn+2]
2.2 Other Identifiers
2.2.1 UNII
9ZV57512ZM
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 598-62-9

2. Manganese(ii) Carbonate

3. Manganous Carbonate

4. Rhodochrosite

5. Manganese Carbonate (1:1)

6. Carbonic Acid, Manganese Salt

7. Manganese(2+) Carbonate

8. Manganese(2+);carbonate

9. Manganese Carbonate (mnco3)

10. 17375-37-0

11. Manganese(2+) Carbonate (1:1)

12. 9zv57512zm

13. Manganese(ii)carbonate

14. Carbonic Acid, Manganese(2+) Salt (1:1)

15. Natural Rhodochrosite

16. Mfcd00011116

17. Ccris 3660

18. Hsdb 790

19. Nsc-83512

20. Einecs 209-942-9

21. Nsc 83512

22. Unii-9zv57512zm

23. Einecs 241-414-3

24. Manganum Carbonicum

25. Ec 209-942-9

26. Rhodochrosite [inci]

27. Schembl32918

28. Dtxsid1042108

29. Manganese Carbonate [mi]

30. Manganese Carbonate [hsdb]

31. Manganum Carbonicum [hpus]

32. Carbonic Acid,manganese Salt

33. Manganese(ii) Carbonate, Mn 44%

34. Manganese Carbonate [who-dd]

35. Manganese(ii) Carbonate, Min. 90%

36. Akos015903237

37. Manganese(ii) Carbonate, P.a., 44%

38. Q414659

39. J-521674

40. Manganese(ii) Carbonate, 99.985% (metals Basis)

41. Manganese(ii) Carbonate, >=99.9% Trace Metals Basis

42. Manganese(ii) Carbonate Hydrate, 44-46% Mn Basis (kt)

43. 11-((5-dimethylaminonaphthalene-1-sulfonyl) Amino)undecanoic

2.4 Create Date
2005-07-19
3 Chemical and Physical Properties
Molecular Weight 114.947 g/mol
Molecular Formula CMnO3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass114.922787 g/mol
Monoisotopic Mass114.922787 g/mol
Topological Polar Surface Area63.2 Ų
Heavy Atom Count5
Formal Charge0
Complexity18.8
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Therapeutic Uses

MANGANESE CARBONATE IS USED IN MEDICINE AS A HEMATINIC

Venugopal, B. and T.D. Luckey. Metal Toxicity in Mammals, 2. New York: Plenum Press, 1978., p. 263


5 Pharmacology and Biochemistry
5.1 FDA Pharmacological Classification
5.1.1 Pharmacological Classes
Paramagnetic Contrast Agent [EPC]; Magnetic Resonance Contrast Activity [MoA]
5.2 Absorption, Distribution and Excretion

The subcellular distribution of manganese (Mn) in brains of mice chronically admin Mn in different chemical forms with food was examined using gel chromatography. Male ddY-mice were divided into five groups of six animals each, & Groups 1 to 4 were given 2 grams/kilogram Mn of standard laboratory mouse chow) in the form of manganese chloride (MnCl2), manganese acetate (MnAc), manganese carbonate (MnCO3), or manganese oxide (MnO2), in the diets for 12 months, while Group 5 served as control. 24 hr after the last feed, animals were decapitated & brains were rapidly removed for study of the different regions (corpus striatum (CS), hypothalamus, midbrain, cerebral cortex (CC), hippocampus, cerebellum, & medulla oblongata). Subcellular fractions (mitochondrial, microsomal & cytosolic) & gel chromatography fractions were analyzed for Mn contents using flame atomizer absorption spectrophotometry. Results showed that CC levels of Mn in mice exposed to the nearly insoluble MnCO3 & MnO2 were higher than in controls, while Mn concns in the CS were similar to those in controls. Microsomal Mn in treated mice was also higher than in controls. The gel chromatographic profile of CS showed that 20% Mn was in the high molecular weight (MW) fractions, 45% was in the middle MW fractions, while 32% was in the low MW fractions. The % Mn in high MW fractions was higher (29% to 49%) in the Mn treated groups, than in controls. The % of Mn in low MW fractions of the MnO2 exposed group (9%) was lower than in the MnCl2, MnAc, & MnCO3 exposed groups (42%, 36%, & 38%, respectively). The authors conclude that the brain regional distribution of Mn from the virtually insoluble cmpds is different from that of soluble Mn cmpds, & that striatal subcellular & gel chromatographic profiles are similar for the divalent Mn cmpds. They add that there is more Mn associated with fast migrating ligands in the striatal cytosol of the Mn treated groups than in the controls, & that these binding characteristics are different from those of other organs.

PMID:8475509 Komura J et al.; Toxicology Letters 66 (3): 287-294 (1993)


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