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Sodium borohydride

ALDRICH/452882 - powder, ≥98.0%

Synonym: Sodium tetrahydridoborate

CAS Number: 16940-66-2
Empirical Formula (Hill Notation): H4BNa
Molecular Weight: 37.83
EC Number: 241-004-4
MDL Number: MFCD00003518
Linear Formula: NaBH4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-452882-5G 5 g
$78.50
1/EA
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45-452882-25G 25 g
$82.80
1/EA
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45-452882-100G 100 g
$99.10
1/EA
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45-452882-500G 500 g
$471.00
1/EA
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45-452882-2KG 2 kg
$918.00
1/EA
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45-452882-10KG 10 kg
$0.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 452882-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 452882-500G

 

assay ≥98.0%
cation traces Fe: ≤5 ppm
contains 0.45-0.70% Magnesium carbonate as anticaking agent
form powder
greener alternative category  , Enabling 
greener alternative product characteristics Design for Energy Efficiency
Learn more about the Principles of Green Chemistry .
impurities ≤100 ppm Silica
InChI 1S/BH4.Na/h1H4;/q-1;+1
InChI key YOQDYZUWIQVZSF-UHFFFAOYSA-N
mp >300 °C (dec.) (lit.)
Quality Level 300 
reaction suitability reagent type: reductant
SMILES string [BH4-].[Na+]
sustainability Greener Alternative Product
Application: Sodium borohydride can be used as a reducing agent:        
•  To prepare saturated alcohols by the reduction of conjugated aldehydes and ketones.        
•  Along with Raney nickel for the reduction of aromatic nitro compounds to arylamines.        
•  In the synthesis of secondary amines by reductive amination of ketones and aldehydes in the presence of an acid catalyst.       
•  In the synthesis of δ and γ lactones by the reduction of cyclic anhydrides.       
•  For the chemoselective reduction of N -protected amino acids and peptides to corresponding alcohols.

General description: Sodium borohydride (NaBH4) is the most commonly available borohydride, synthesized by reacting methylborate with sodium hydride in mineral oil. It is employed as a precursor for producing other metal borohydrides. Various approaches for qualitative and quantitative monitoring of sodium borohydride have been explained. The potential of NaBH4 to store as well as generate hydrogen for fuel cells has been investigated.
General description: We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here .
Legal Information: ASCENSUS SPECIALTIES LLC
Packaging: 2 kg in steel drum
Packaging: 5, 25, 100, 500 g in poly bottle
Purity ≥98.0%
mp >300 °C (dec.) (lit.)
UNSPSC 12352302

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