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Home > Products >  Sodium triacetoxyborohydride

Sodium triacetoxyborohydride CAS NO.56553-60-7

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Quick Details

  • ProName: Sodium triacetoxyborohydride
  • CasNo: 56553-60-7
  • Molecular Formula: C6H10BNaO6
  • Appearance: White crystalline powder
  • Application: used as activators for reducing aminat...
  • DeliveryTime: 7-14 days after advanced payment
  • PackAge: 25kg/woven bag
  • Port: Any port in China
  • ProductionCapacity: 1000 Metric Ton/Month
  • Purity: 97%min
  • Storage: dry and ventilated warehouse
  • Transportation: by sea,by air,by courier
  • LimitNum: 0 Metric Ton
  • Grade: Industrial Grade

Superiority

 

 

English name: Sodium triacetoxyborohydride

CAS NO: 56553-60-7

Molecular weight: 211.94

Molecular formula: C6H10BNaO6

Appearance: White crystalline powder

 

Specification: 97%

 

Packing: 25kg per drum

 

Introduction: It has good general suitability and options. It has no pollution for environments.

 

Use: used as activators for reducing amination.

 

Details

 

Package

Packing: foil bag

1.Trade name: Sodium triacetoxyborohydride

2.CAS NO. 56553-60-7

3. Application: used as a reducing agent in organic synthesis

Basic information

Chemical name

              Sodium triacetoxyborohydride

Molecular Formula

C6H10BNaO6

Molecular Weight

211.9408

Solubility

reacts with water

Melting Point

116-120 °C

Purity

>98%

Appearance

white powder

CAS NO.

                          62613-82-5

Application

used as a reducing agent in organic synthesis

Usage

Sodium triacetoxyborohydride, also known as sodium triacetoxyhydroborate, commonly abbreviated STAB, is a chemical compound with the formula Na(CH3COO)3BH. Like other borohydrides, it is used as a reducing agent in organic synthesis. This colourless salt is prepared by protonolysis of sodium borohydride with acetic acid:

NaBH4 + 3 HO2CCH3 → NaBH(O2CCH3)3 + 3 H2

Owing to the steric and electronic effects of the acetoxy groups, sodium triacetoxyborohydride is a milder reducing agent than sodium borohydride or even sodium cyanoborohydride. Furthermore, NaBH(OAc)3 avoids the toxic side-products generated by sodium cyanoborohydride. Sodium triacetoxyborohydride is especially suitable for reductive aminations of aldehydes and ketones.

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