Difference between revisions of "Barium manganate"

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'''Barium manganate''', BaMnO<sub>4</sub>, is a grey-green solid, insoluble in most common solvents. It is used as an [[oxidizing agent]] in [[organic synthesis]].
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{{chembox
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| IUPACName = barium manganate(VI)
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| Section1 = {{Chembox Identifiers
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|  CASNo = 7787-35-1
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|  EINECS = 232-109-6
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|  ChemSpiderID = 2341155
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  }}
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| Section2 = {{Chembox Properties
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|  Reference = <ref>{{RubberBible62nd|page=B-81}}.</ref>
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|  Formula = BaMnO<sub>4</sub>
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|  MolarMass = 256.26 g mol<sup>−1</sup>
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|  Appearance = grey-green powder
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|  Density = 4.85 g cm<sup>−3</sup>
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|  Solubility = insoluble
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  }}
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| Section7 = {{Chembox Hazards
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|  Reference = <ref name="CLP">{{CLP Regulation|index=056-002-00-7|page=438}}</ref>
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|  EUIndex = 056-002-00-7
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|  GHSPictograms = {{GHS07|Acute Tox. 4 (oral, inhal.)}}
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|  GHSSignalWord = WARNING
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|  HPhrases = {{H-phrases|302|332}}
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|  PPhrases = {{P-phrases|261|264|270|271|301+312|304+340|330|501}}
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  }}
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}}
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'''Barium manganate''', BaMnO<sub>4</sub>, is a grey-green solid, insoluble in most common solvents. It is used as an [[oxidizing agent]] in [[organic synthesis]].<ref>{{citation | first1 = G. | last1 = Procter | first2 = S. V. | last2 = Ley | first3 = G. H. | last3 = Castle | contribution = Barium Manganate | title = Encyclopedia of Reagents for Organic Synthesis | editor-first = L. | editor-last = Paquette | year = 2004 | publisher = Wiley | location = New York | doi = 10.1002/047084289}}.</ref><ref>{{citation | title = Barium Manganate. A Versatile Oxidant in Organic Synthesis | first1 = Habib | last1 = Firouzabadi | first2 = Zohreh | last2 = Mostafavipoor | journal = Bull. Chem. Soc. Jpn. | volume = 56 | issue = 3 | year = 1983 | pages = 914–17 | doi = 10.1246/bcsj.56.914}}.</ref><ref>{{citation | last1 = Guziec | first1 = Frank S., Jr. | last2 = Murphy | first2 = Christopher J. | last3 = Cullen | first3 = Edward R. | title = Thermal and photochemical studies of symmetrical and unsymmetrical dihydro-1,3,4-selenadiazoles | journal = J. Chem. Soc., Perkin Trans. 1 | year = 1985 | pages = 107–13 | doi = 10.1039/P19850000107}}.</ref>
  
 
==References==
 
==References==
 
{{reflist}}
 
{{reflist}}
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==External links==
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*{{EHC|107|name=Barium}}
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*{{HSG|046|name=Barium}}
  
 
[[Category:Barium compounds]]
 
[[Category:Barium compounds]]

Latest revision as of 11:53, 8 January 2011

Barium manganate
IUPAC name barium manganate(VI)
Identifiers
CAS number [7787-35-1]
EC number 232-109-6
ChemSpider 2341155
Properties[1]
Chemical formula BaMnO4
Molar mass 256.26 g mol−1
Appearance grey-green powder
Density 4.85 g cm−3
Solubility in water insoluble
Hazards[2]
EU index number 056-002-00-7
GHS pictograms Acute Tox. 4 (oral, inhal.)
GHS signal word WARNING
GHS hazard statements H302, H332
GHS precautionary statements P261, P264, P270, P271, P301+312, P304+340, P330, P501
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Barium manganate, BaMnO4, is a grey-green solid, insoluble in most common solvents. It is used as an oxidizing agent in organic synthesis.[3][4][5]

References

  1. CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-81. ISBN 0-8493-0462-8.
  2. Index no. 056-002-00-7 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at p 438.
  3. Procter, G.; Ley, S. V.; Castle, G. H. Barium Manganate. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L., Ed.; Wiley: New York, 2004. DOI: 10.1002/047084289.
  4. Firouzabadi, Habib; Mostafavipoor, Zohreh Barium Manganate. A Versatile Oxidant in Organic Synthesis. Bull. Chem. Soc. Jpn. 1983, 56 (3), 914–17. DOI: 10.1246/bcsj.56.914.
  5. Guziec, Frank S., Jr.; Murphy, Christopher J.; Cullen, Edward R. Thermal and photochemical studies of symmetrical and unsymmetrical dihydro-1,3,4-selenadiazoles. J. Chem. Soc., Perkin Trans. 1 1985, 107–13. DOI: 10.1039/P19850000107.

External links

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