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Manufacturer of Bronopol - Factory supply best price Sodium triacetoxyborohydride powder CAS 56553-60-7 – Zoran

Manufacturer of Bronopol - Factory supply best price Sodium triacetoxyborohydride powder CAS 56553-60-7 – Zoran

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Our company since its inception, always regards product quality as enterprise life, continuously improve production technology, improve product quality and continuously strengthen enterprise total quality management, in strict accordance with the national standard ISO 9001:2000 for Cas 10025-99-7, Cas 2052-49-5, Carbon Nanotube Swcnt, Our highly specialized process eliminates the component failure and offers our customers unvarying quality, allowing us to control cost, plan capacity and maintain consistent on time delivery.
Manufacturer of Bronopol - Factory supply best price Sodium triacetoxyborohydride powder CAS 56553-60-7 – Zoran Detail:

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Safe shipping way CAS 56553-60-7 powder Sodium triacetoxyborohydride
Product name: Sodium triacetoxyborohydride
CAS: 56553-60-7
Molecular formula: C6H10BNaO6
Appearance: white powder
Content: 95.0%~105.0%(titration)
Uses: For amination reduction reaction of ketone and aldehyde, reductive amination or lactamization of carbonyl compound and amine, and reductive amination of aryl aldehyde
Capacity: 5~10mt/month

Sodium triacetoxyborohydride (STAB) CAS 56553-60-7 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.

However, unlike sodium cyanoborohydride, the triacetoxyborohydride is water-sensitive, and water cannot be used as a solvent with this reagent, nor is it compatible with methanol. It reacts only slowly with ethanol and isopropanol and can be used with these. NaBH(OAc)3 may also be used for reductive alkylation of secondary amines with aldehyde-bisulfite adducts.

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