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455571

Sigma-Aldrich

Potassium borohydride

≥97%

Synonym(s):

Potassium tetrahydroborate

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About This Item

Linear Formula:
KBH4
CAS Number:
13762-51-1
Molecular Weight:
53.94
EC Number:
237-360-5
MDL number:
MFCD00011396
UNSPSC Code:
12352306
PubChem Substance ID:
24868580
NACRES:
NA.22

Quality Level

200

Assay

≥97%

form

powder

reaction suitability

reagent type: reductant

mp

500 °C (dec.) (lit.)

density

1.18 g/mL at 25 °C (lit.)

SMILES string

[K+].[H][B-]([H])([H])[H]

InChI

1S/BH4.K/h1H4;/q-1;+1

InChI key

ICRGAIPBTSPUEX-UHFFFAOYSA-N

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Application

Potassium borohydride (KBH4) can be used as a reducing agent for the synthesis of:       
  • Copper nanoparticles by the reduction of copper salts.
  •  Enantioselective allylic alcohols by the catalytic reduction of enones and ketones in the presence of chiral N,N′-dioxidescandium(III) complex catalyst.,·        
  • Azoxybenzenes by the reduction of nitroarenes in the presence of phase transfer catalyst PEG-400.

It can also be employed as a boron source in the nickel–boron alloy, which is electrodeposited on carbon fiber to improve catalytic graphitization of carbon.

Signal Word

Danger

Hazard Statements

H260,H301,H314,H360FD

Hazard Classifications

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

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Catalytic graphitization of carbon fibers with electrodeposited Ni-B alloy coating
Zhou H, et al.
Materials Chemistry and Physics, 110(2-3), 434-439 (2008)
Peng He et al.
Organic letters, 14(19), 5134-5137 (2012-09-28)
The first catalytic enantioselective 1,2-reduction of enones with 0.45 mol equiv potassium borohydride solution catalyzed by a chiral N,N'-dioxide-Sc(III) complex catalyst was accomplished under mild reaction conditions. A number of optically active allylic alcohols were obtained in good to excellent
Preparation of copper nanoparticles by chemical reduction method using potassium borohydride
Zhang Q-L, et al.
Transactions of Nonferrous Metals Society of China, 20, 240-s244-240-s244 (2010)
A P Seddon et al.
The Journal of biological chemistry, 261(25), 11538-11543 (1986-09-05)
Bacterial 5-oxoprolinase is composed of two protein components: Component A, which catalyzes 5-oxoproline-dependent ATP-hydrolysis and Component B, which couples the hydrolysis of ATP with the decyclization of 5-oxoproline to form glutamate (Seddon, A. P., Li, L., and Meister, A. (1984)
Chuan Zhang et al.
Analytica chimica acta, 652(1-2), 143-147 (2009-09-30)
Room-temperature ionic liquid in combination with sodium diethyldithiocarbamate (DDTC) was used to synergetically improve the chemical vapor generation (CVG) of nickel. Volatile species of nickel were effectively generated through reduction of acidified analyte solution with KBH(4) in the presence of
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