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329320

Sigma-Aldrich

Bromoform-d

≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer

Synonym(s):

Tribromomethane-d

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About This Item

Linear Formula:
CDBr3
CAS Number:
2909-52-6
Molecular Weight:
253.74
EC Number:
220-823-0
MDL number:
MFCD00000129
UNSPSC Code:
12352005
PubChem Substance ID:
24859783
NACRES:
NA.12

isotopic purity

≥99.5 atom % D

Assay

≥99% (CP)

form

liquid

contains

copper as stabilizer

impurities

~1% carbon tetrabromide

refractive index

n20/D 1.596 (lit.)

bp

136.5 °C (lit.)

density

2.906 g/mL at 25 °C (lit.)

mass shift

M+1

SMILES string

[2H]C(Br)(Br)Br

InChI

1S/CHBr3/c2-1(3)4/h1H/i1D

InChI key

DIKBFYAXUHHXCS-MICDWDOJSA-N

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Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H302,H315,H319,H331,H411

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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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Chao He et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 21(12), 1295-1309 (2020-04-16)
The crossed molecular beam reactions of the methylidyne radical (CH; X2 Π) with 1,3-butadiene (CH2 CHCHCH2 ; X1 Ag ) along with their (partially) deuterated counterparts were performed at collision energies of 20.8 kJ mol-1 under single collision conditions. Combining our laboratory
Chao He et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(48), 30142-30150 (2020-11-18)
Since the postulation of carbenes by Buchner (1903) and Staudinger (1912) as electron-deficient transient species carrying a divalent carbon atom, carbenes have emerged as key reactive intermediates in organic synthesis and in molecular mass growth processes leading eventually to carbonaceous

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