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86-13476104184 Buy Sodium borohydride CAS 16940-66-2 in Australia Local warehouse

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We have warehouse at Moscow, Germany,Canada,USA.and Australia ,Pick up is supported for bulk. factory supply good price.without any shipping problems.

MF:BH4Na,MW:37.83
MOQ:10g
Package:Conventional packing or as your requirments
Shipping way:By air or sea
Sodium borohydride is used as a reagent in the reduction of amino acids and their derivatives. Also used as a catalyst in the ammonia borane dehydrogenation. Sodium borohydride is used as a reducing agent in the synthesis of gold nanoparticles. It is also used for wood pulp and as a blowing agent for plastics. It reduces the aldehyde and keto groups to give the corresponding alcohols

Product Name: Sodium borohydride
Synonyms: VenPure SF;SodiuM borohydride caplets (18 x 10 x 8 MM), 98%;SodiuM borohydride granular, 10-40 Mesh, 98%;SodiuM borohydride granular, 99.99% trace Metals basis;SodiuM borohydride powder, >=98.0%;SodiuM borohydride puruM p.a., >=96% (gas-voluMetric);SodiuM borohydride ReagentPlus(R), 99%;SodiuM borohydride solution 2.0 M in triethylene glycol diMethyl ether
CAS NO: 16940-66-2
Molecular Weight: 37.83
Molecular Formula: BH4Na
Boiling Point: 500°C
Melting point: >300 °C (dec.) (lit.)
Density: 1.035 g/mL at 25 °C
Appearance: White powder
Purity: >98%
Stability: Water Solubility  550 g/L (25 ºC)
Storage: Store at RT.
Sodium Borohydride Molar Mass/Molar Mass Of Sodium Borohydride
37.83
sds sodium borohydride/sodium borohydride sds
Density Of Sodium Borohydride/Sodium Borohydride Density
1.035 g/mL at 25 °C
Sodium Borohydride Boiling Point
500°C
Reduction By Sodium Borohydride/ Sodium Borohydride Reduction Mechanism
Sodium borohydride is a relatively selective reducing agent. Ethanolic solutions of sodium borohydride reduce aldehydes and ketones in the presence of epoxides, esters, lactones, acids, nitriles, or nitro groups. Reduction of aldehydes is straightforward.Sodium borohydride will reduce aldehydes to primary alcohols and ketones to secondary alcohols. This proceeds via a two-step mechanism consisting of 1) nucleophilic addition, followed by 2) protonation. Esters and amides are not reduced by NaBH4 under normal conditions.

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