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Sigma-Aldrich

o-Carborane

98%

Synonym(s):

1,2-Dicarbadodecaborane(12)

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About This Item

Empirical Formula (Hill Notation):
C2H12B10
CAS Number:
Molecular Weight:
144.23
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

Assay

98%

mp

260 °C (subl.) (lit.)

storage temp.

2-8°C

SMILES string

[bH]1[bH][bH][bH][bH][bH]cc[bH][bH][bH][bH]1

InChI

1S/C2H12B10/c1-2-4-6-8-10-12-11-9-7-5-3-1/h1-12H/b2-1-

InChI key

PWHTZDUTEHXWHV-UPHRSURJSA-N

General description

Electron deficient boron cage compounds with one or more carbon atoms as a ligand in the borane framework. The three common isomers are o-carborane, m-carborane and p-carborane 1The structure could be polyhedral or open cage.

Packaging

Packaged in glass bottles

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Yin-Ping Wang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(8), 1814-1819 (2016-11-30)
Palladium(II)-induced selective B(4)-H activation of an o-carboranylthioamide has been developed. A tetranuclear palladium(II) complex has been obtained in high yield with excellent regioselectivity. DFT calculations have confirmed that the B(4)-borometalate is lower in energy than the corresponding B(3)-borometalate. The product
Temidayo O B Olusanya et al.
Biophysical chemistry, 247, 25-33 (2019-02-24)
Based on the promise of liposomes as convenient vehicles for the transport of boronated agents for the boron neutron capture therapy (BCNT) of cancer, this paper reports a method for the formulation and characterisation of stable o-carborane-loaded liposomes (ca. 80-100 nm)
Issei Takeuchi et al.
Colloids and surfaces. B, Biointerfaces, 159, 360-365 (2017-08-15)
Poly(DL-lactide-co-glycolide) (PLGA) has been widely used and studied because of its biocompatibility and biodegradability. Recently, the usefulness of nanoparticles using poly(L-lactide-co-glycolide) (PLLGA) having a higher glass transition temperature than PLGA was suggested. In this study, we investigated the availability of

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