10387-40-3 Potassiu...

10387-40-3 Potassium thioacetate

10387-40-3 Potassium thioacetate

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1 Kilogram

FOB Price: USD 500.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T

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10387-40-3 Potassium thioacetate 10387-40-3 Potassium thioacetate 10387-40-3 Potassium thioacetate

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  • Appearance:Powder
  • Application:Organic Chemicals
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  • ProductionCapacity:100|Metric Ton|Day
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Product Name: Potassium thioacetate
Synonyms: Potassium thioaccetate;Potasium thioacetate;Potassium thioacetat;PotassiuM thioacetate, 98% 25GR;PotassiuM thioacetate, 98% 5GR;MeCOSK;potassium 2-thioxoacetate;MERCAPTOACETIC ACID, POTASSIUM SALT
CAS: 10387-40-3
MF: C2H3KOS
MW: 114.21
EINECS: 233-848-7
Product Categories: Pharmaceutical intermediates
Mol File: 10387-40-3.mol

Potassium thioacetate Chemical Properties
Melting point  173-176 °C(lit.)
density  1.58 g/cm3
storage temp.  Refrigerator (+4°C)
solubility  soluble
form  Crystalline Powder, Crystals or Chunks
color  White to light brown
Water Solubility  soluble
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions
Sensitive  Air Sensitive & Hygroscopic
BRN  3595448
CAS DataBase Reference 10387-40-3(CAS DataBase Reference)
EPA Substance Registry System Ethanethioic acid, potassium salt (10387-40-3)
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
RIDADR  UN 3335
WGK Germany  3
F  3-9-13-23
TSCA  Yes
HazardClass  9
HS Code  29309070

Potassium thioacetate Usage And Synthesis
Chemical Properties white to light brown crystalline powder, crystals
Uses Potassium Thioacetate is the potassium salt of Thioacetic Acid, a commonly used reagent in organic synthesis for the introduction of thiol groups in molecules.
Application Potassium thioacetate is an organosulfur compound and a salt with the formula CH3COS−K+. This white, water-soluble solid is used as a reagent for preparing thioacetate esters and other derivatives . It acts as a sulfur source in the synthesis of sulfur-containing organic compounds for the synthesis of heterocycles, polymers, transition-metal ligands, nanoparticles, bioactive compounds and macromolecular inclusion complexes. It is also used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives and it is also used as a reagent in the conversion of halides to thiols.

Details:


Product Name: Potassium thioacetate
Synonyms: Potassium thioaccetate;Potasium thioacetate;Potassium thioacetat;PotassiuM thioacetate, 98% 25GR;PotassiuM thioacetate, 98% 5GR;MeCOSK;potassium 2-thioxoacetate;MERCAPTOACETIC ACID, POTASSIUM SALT
CAS: 10387-40-3
MF: C2H3KOS
MW: 114.21
EINECS: 233-848-7
Product Categories: Pharmaceutical intermediates
Mol File: 10387-40-3.mol

Potassium thioacetate Chemical Properties
Melting point  173-176 °C(lit.)
density  1.58 g/cm3
storage temp.  Refrigerator (+4°C)
solubility  soluble
form  Crystalline Powder, Crystals or Chunks
color  White to light brown
Water Solubility  soluble
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions
Sensitive  Air Sensitive & Hygroscopic
BRN  3595448
CAS DataBase Reference 10387-40-3(CAS DataBase Reference)
EPA Substance Registry System Ethanethioic acid, potassium salt (10387-40-3)
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
RIDADR  UN 3335
WGK Germany  3
F  3-9-13-23
TSCA  Yes
HazardClass  9
HS Code  29309070

Potassium thioacetate Usage And Synthesis
Chemical Properties white to light brown crystalline powder, crystals
Uses Potassium Thioacetate is the potassium salt of Thioacetic Acid, a commonly used reagent in organic synthesis for the introduction of thiol groups in molecules.
Application Potassium thioacetate is an organosulfur compound and a salt with the formula CH3COS−K+. This white, water-soluble solid is used as a reagent for preparing thioacetate esters and other derivatives . It acts as a sulfur source in the synthesis of sulfur-containing organic compounds for the synthesis of heterocycles, polymers, transition-metal ligands, nanoparticles, bioactive compounds and macromolecular inclusion complexes. It is also used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives and it is also used as a reagent in the conversion of halides to thiols.

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