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288187

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:
16872-09-6
Molecular Weight:
144.23
EC Number:
240-897-8
MDL number:
MFCD00012169
UNSPSC Code:
12352300
PubChem Substance ID:
24857324
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

Related Categories

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
GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS9949
MKCJ7821
03724BH
00618AH
02024BE

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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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