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hot sale low price supply Sodium cyanoborohydride

hot sale low price supply Sodium cyanoborohydride

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  • Min.Order :0 Metric Ton
  • Purity: 98%
  • Payment Terms : L/C,T/T

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Quick Details

  • Appearance:white powder
  • Application:Pharm intermediates
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  • ProductionCapacity:|Metric Ton|Day
  • Storage:kept in a cool, dry and ventilated place
  • Transportation:By Sea,by Air,By courier like DHL or Fedx

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Details:

Sodium cyanoborohydride Basic information
Product Name: Sodium cyanoborohydride
Synonyms: (cyano-C)trihydro-,sodium,(T-4)-Borate(1-);sodium,(beta-4)-borate(1-(cyano-c)trihydro-;SODIUM CYANOBOROHYDRIDE;SODIUM CYANOTRIHYDRIDOBORATE;SODIUM CYANOTRIHYDROBORATE;Sodium cyonobrohydriole;SODIUM CYANOBOROHYDRIDE, 5.0M SOLUTION I N AQUEOUS CA. 1M SODIUM HYDROXIDE;SODIUM CYANOBOROHYDRIDE, 1.0M SOLUTION I N TETRAHYDROFURAN
CAS: 25895-60-7
MF: CH3BNNa
MW: 62.84
EINECS: 247-317-2
Product Categories: Selectivity reducing agent;B (Classes of Boron Compounds);Classes of Metal Compounds;Na (Sodium) Compounds (excluding simple sodium salts);Reduction;Synthetic Organic Chemistry;Tetrahydroborates;Typical Metal Compounds;Borohydrides;Synthetic Reagents;borane
Mol File: 25895-60-7.mol
Sodium cyanoborohydride Structure
 
Sodium cyanoborohydride Chemical Properties
Melting point  >242 °C (dec.)(lit.)
Boiling point  307°C
density  1.083 g/mL at 25 °C
Fp  −1 °F
storage temp.  Store under Argon
solubility  H2O: may be clear to slightly hazy
Water Solubility  2120 g/L at 29 ºC (dec.)
Sensitive  Moisture Sensitive
Merck  14,8606
Stability: Stable. Hygroscopic. Reacts violently with water, giving off and igniting hydrogen. Do not use water on fires involving this chemical - instead use dry soda ash. Incompatible with strong acids, water, strong oxidizing agents.
CAS DataBase Reference 25895-60-7(CAS DataBase Reference)
EPA Substance Registry System Borate(1-), (cyano-.kappa.C)trihydro-, sodium, (T-4)-(25895-60-7)
 
Sodium cyanoborohydride Usage And Synthesis
Chemical Properties White solid
Uses Sodium Cyanoborohydride is a commonly used as a reagent in the reductive amination of aldehydes and ketones and in the reductive alkylation of amines.
 

 

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