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463051

Sigma-Aldrich

Diborane

99.99% (diborane only), 9-11% (balance hydrogen), 10% in hydrogen, electronic grade

Synonym(s):

Borane (B2 H6 ), Boron hydride (B2 H6 ), Diboron hexahydride

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About This Item

Linear Formula:
B2H6
CAS Number:
Molecular Weight:
27.67
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

grade

electronic grade

Assay

99.99% (diborane only)

form

gas

reaction suitability

reagent type: reductant

concentration

10% in hydrogen
9-11% (balance hydrogen)

bp

−92.5 °C (lit.)

SMILES string

BB

InChI

1S/B2H4/c1-2/h1-2H2

InChI key

QSJRRLWJRLPVID-UHFFFAOYSA-N

General description

Atomic number of base material: 5 Boron

Application

Dibrorane gas is used primarily as a p-type dopant in the deposition of eptaxial and amorphous silicon thin films.
Useful as a p-type dopant for the deposition of silicon-containing thin films.

Packaging

Supplied in a carbon steel lecture bottle with a CGA180M/CGA110F needle valve installed.

Compatible with the following:
  • Aldrich® lecture-bottle station systems
  • Aldrich® lecture-bottle gas regulators

Other Notes

Legal Information

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC

hose barb

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purge valve

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Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Flam. Gas 1

Storage Class Code

2A - Gases

WGK

WGK 3

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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Q Zhao et al.
Nano letters, 5(5), 847-851 (2005-05-12)
Novel carbon nanotube-metal cluster structures are proposed as prototype systems for molecular recognition at the nanoscale. Ab initio calculations show that already the bare nanotube cluster system displays some specificity because the adsorption of ammonia on a carbon nanotube-Al cluster
O H Griffith et al.
Ultramicroscopy, 6(2), 149-156 (1981-01-01)
The relative brightness of photoelectron microscopy images as a function of exposure to UV light has been determined from model systems representative of biological cell surface components. Quantitative data for amino acid homopolymers, yields. The photoelectron quantum yields, increase substantially
Holger Braunschweig et al.
Angewandte Chemie (International ed. in English), 50(52), 12613-12616 (2011-11-08)
The diboranes(4) bis(catecholato)diborane (B(2)Cat(2)) and bis(pinacolato)diborane (B(2)Pin(2)) are important precursors for organoboronic esters, which are versatile reagents for the formation of carbon-carbon bonds. A new catalytic synthesis for these compounds starts from catecholborane or pinacolborane and gives the dehydrocoupling products
P P Kung et al.
Biotechnology and bioengineering, 61(2), 119-125 (1999-04-01)
Several piperazine libraries were prepared using solution phase simultaneous addition of functionalities methodology as well as the "library from library" concept. The resulting piperazine libraries displayed antimicrobial activity against both gram-positive and gram-negative bacteria.
Kasper T Møller et al.
Dalton transactions (Cambridge, England : 2003), 46(35), 11905-11912 (2017-08-30)
A new synthesis method of samarium borohydride, Sm(BH

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