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Dipotassium osmate

Base Information
  • Chemical Name:Dipotassium osmate
  • CAS No.:19718-36-6
  • Deprecated CAS:39319-62-5
  • Molecular Formula:K. 1/2 O4 Os
  • Molecular Weight:876.90996
  • Hs Code.:
  • European Community (EC) Number:243-247-1
  • UNII:CNI6UL5029
  • Wikipedia:Potassium_osmate
  • Wikidata:Q4338050
Dipotassium osmate

Synonyms:Dipotassium osmate;19718-36-6;Potassium osmate(VI);dipotassium;dioxido(dioxo)osmium;UNII-CNI6UL5029;Osmate (OsO42-), dipotassium, (T-4)-;CNI6UL5029;Potassium(VI) osmiate dihydrate;EINECS 243-247-1;Osmic acid (H2OsO4), dipotassium salt;Osmate (OsO42-), potassium (1:2), (T-4)-;potassium osmate;K.1/2O4Os;K.1/2O4-Os;Potassium osmate(VI) 2-hydrate;JMVOCSLPMGHXPG-UHFFFAOYSA-N;POTASSIUM OSMATE(VI) [MI];DIPOTASSIUM OSMIUM TETRAOXIDE;AKOS040768403;DIPOTASSIUM TETRAOXOOSMATE(2-);Q4338050;Potassium tetrahydroxodioxoosmate(VI) inverted exclamation mark degrees Potassium Osmate inverted exclamation mark+/-

Suppliers and Price of Dipotassium osmate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 14 raw suppliers
Chemical Property of Dipotassium osmate
Chemical Property:
  • PSA:68.28000 
  • LogP:-0.47520 
  • Water Solubility.:soluble H2O; insoluble alcohol, ether [MER06] 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:333.86855
  • Heavy Atom Count:7
  • Complexity:62.2
Purity/Quality:

98%,99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 23/24/25 
  • Safety Statements: 22-26-36-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Metals -> Metals, Inorganic Compounds
  • Canonical SMILES:[O-][Os](=O)(=O)[O-].[K+].[K+]
Refernces

Facile synthesis of hydroxymethylcytosine-containing oligonucleotides and their reactivity upon osmium oxidation

10.1039/c1ob05247k

The research aims to develop a facile synthesis method for hydroxymethylcytosine (hmC)-containing oligonucleotides (ODNs) and investigate their reactivity upon osmium oxidation. The study synthesizes hmC-containing ODNs using a straightforward route starting from thymidine and involving protection, bromination, and amination steps, ultimately converting the nucleoside into phosphoramidite form for DNA autosynthesizer use. The synthesized ODNs form stable duplexes with complementary DNA, exhibiting similar melting temperatures and enzymatic digestion properties to methylated counterparts. Osmium oxidation, a method previously used for detecting 5-methylcytosine (mC), is tested on hmC-containing ODNs under specific reaction conditions, revealing that hmC is oxidized as efficiently as mC, forming a stable ternary complex. The study concludes that osmium oxidation is a viable method for detecting hmC in DNA, potentially advancing epigenetic studies. Key chemicals used include thymidine, acetic anhydride, N-bromosuccinimide, 3-hydroxypropionitrile, phosphorus oxychloride, ammonia, di(n-butyl)formamidine, potassium osmate, potassium hexacyanoferrate(III), and bipyridine.

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