452882

Sodium borohydride

powder, ≥98.0%

Manufacturer: Sigma Aldrich

CAS Number: 16940-66-2

Synonym(S): Sodium tetrahydridoborate

Select a Size

Pack Size SKU Availability Price
5 G 452882-5-G In Stock ₹ 7,220.28
25 G 452882-25-G In Stock ₹ 7,609.98
100 G 452882-100-G In Stock ₹ 10,023.95
6 X 25 G 452882-6-X-25-G In Stock ₹ 10,424.48
6 X 100 G 452882-6-X-100-G In Stock ₹ 20,058.73
500 G 452882-500-G In Stock ₹ 24,074.80
2 KG 452882-2-KG In Stock ₹ 84,337.58

452882 - 5 G

₹ 7,220.28

In Stock

Quantity

1

Base Price: ₹ 7,220.28

GST (18%): ₹ 1,299.65

Total Price: ₹ 8,519.93

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 EfficiencyLearn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

impurities

≤100 ppm Silica

mp

>300 °C (dec.) (lit.)

cation traces

Fe: ≤5 ppm

Other Options

Image Product Name Manufacturer Price Range
1.06371
Sodium borohydride
Supelco ₹ 38,710.01
80546
Sodium borohydride
Supelco ₹ 10,803.35 - ₹ 30,862.08
480886
Sodium borohydride
Sigma Aldrich ₹ 18,142.70 - ₹ 39,597.85

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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]
  • 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]
  • Legal Information: ASCENSUS SPECIALTIES LLC

SAFETY INFORMATION

Pictograms

GHS02,GHS06,GHS08,GHS05

Signal Word

Danger

Hazard Statements

H260,H301,H314,H360FD

Precautionary Statements

P231 + P232 - P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Water-react 1

Supplementary Hazards

EUH014

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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0.45-0.70% Magnesium carbonate as anticaking agent

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reagent type: reductant

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Design for Energy EfficiencyLearn more about the Principles of Green Chemistry.

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