Sigma-Aldrich 452882 Sodium borohydride powder, ≥98.0% 6 x 25 gr
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Marka
Stok Kodu
LB.SA.452882-6X25G
Kısa Bilgi
Synonym(s): Sodium tetrahydridoborate Linear Formula: NaBH4 CAS Number: 16940-66-2 Molecular Weight: 37.83 EC Number: 241-004-4 MDL number: MFCD00003518 PubChem Substance ID: 57650269 NACRES: NA.22
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Sigma-Aldrich 452882 Sodium borohydride powder, ≥98.0% 6 x 25 gr |
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Synonym(s): Sodium tetrahydridoborate
Linear Formula: NaBH4
CAS Number: 16940-66-2
Molecular Weight: 37.83
EC Number: 241-004-4
MDL number: MFCD00003518
PubChem Substance ID: 57650269
NACRES: NA.22
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PROPERTIES
Quality Level 300
assay ≥98.0%
form powder
contains 0.45-0.70% Magnesium carbonate as anticaking agent
reaction suitability reagent type: reductant
greener alternative product characteristics Design for Energy Efficiency Learn more about the Principles of Green Chemistry.
impurities ≤100 ppm Silica
mp >300 °C (dec.) (lit.)
cation traces Fe: ≤5 ppm
greener alternative category Enabling
SMILES string [BH4-].[Na+]
InChI 1S/BH4.Na/h1H4;/q-1;+1
InChI key YOQDYZUWIQVZSF-UHFFFAOYSA-N
DESCRIPTION
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.[1] The potential of NaBH4 to store as well as generate hydrogen for fuel cells has been investigated.[2][3] 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.
Application
Sodium borohydride can be used as a reducing agent:
To prepare saturated alcohols by the reduction of conjugated aldehydes and ketones.[4]
Along with Raney nickel for the reduction of aromatic nitro compounds to arylamines.[5]
In the synthesis of secondary amines by reductive amination of ketones and aldehydes in the presence of an acid catalyst.[6]
In the synthesis of δ and γ lactones by the reduction of cyclic anhydrides.[7]
For the chemoselective reduction of N -protected amino acids and peptides to corresponding alcohols.[8]
Packaging
5, 25, 100, 500 g in poly bottle
2 kg in steel drum
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