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Safety Information

B4388

Sigma-Aldrich

2-Bromo-2-chloro-1,1,1-trifluoroethane

≥99%

Synonym(s):

Halothane

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100 MG
CN¥9,609.75

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100 MG
CN¥9,609.75

About This Item

Linear Formula:
BrCH(Cl)CF3
CAS Number:
Molecular Weight:
197.38
Beilstein:
1736947
EC Number:
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.77

CN¥9,609.75


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vapor pressure

4.5 psi ( 20 °C)

Quality Level

Assay

≥99%

form

liquid

contains

0.01% thymol as stabilizer

refractive index

n20/D 1.369 (lit.)

bp

50.2 °C (lit.)

density

1.872 g/mL at 25 °C (lit.)

SMILES string

FC(F)(F)C(Cl)Br

InChI

1S/C2HBrClF3/c3-1(4)2(5,6)7/h1H

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This Item
684449684430684465
assay

>99.9%

assay

>99.5%

assay

>99%

assay

99%

semiconductor properties

N-type (mobility=0.21 cm2/V·s)

semiconductor properties

N-type (mobility=0.21 cm2/V·s)

semiconductor properties

N-type (mobility=0.21 cm2/V·s)

semiconductor properties

N-type (mobility=0.1 cm2/V·s)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

solid

form

solid

form

powder

form

powder

description

functionalized fullerene

description

functionalized fullerene

description

functionalized fullerene

description

-

solubility

chlorobenzene: soluble

solubility

-

solubility

chlorobenzene: soluble, organic solvents: soluble, toluene: soluble

solubility

chlorobenzene: soluble, organic solvents: soluble, toluene: soluble

Application

2-Bromo-2-chloro-1,1,1-trifluoroethane, or halothane, has been used in a study that combined molecular simulations with free energy simulations to study solvation of halothane in polarizable water and methanol. Halothane has also been used in a study to investigate the interaction of anesthetics with the Rho GTPase regulator Rho GDP dissociation inhibitor.

Biochem/physiol Actions

2-Bromo-2-chloro-1,1,1-trifluoroethane is an inhalation anesthetic. In an effect believed to be independent of anesthesia, halothane inhibits the synthesis of 5-hydroxytryptamine in brain tissue, probably at the tryptophan hydroxylase step.
Inhalation anesthetic.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Repr. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Trimethyl borate-induced one-pot homologation reactions of isoquinoline with di-tert-butyl-TMP zincate
Seo HJ, et al.
Tetrahedron Letters, 52(29), 3747-3750 (2011)
Trimethyl borate as an electrolyte additive for high potential layered cathode with concurrent improvement of rate capability and cyclic stability
Wang Z, et al.
Electrochimica Acta, 184(1), 40-46 (2015)
Thermal-heating CVD synthesis of BN nanotubes from trimethyl borate and nitrogen gas.
Lin FH, et al.
Materials Chemistry and Physics, 107(1), 115-121 (2008)
One-Pot Synthesis of Ammonia-Borane and Trialkylamine-Boranes from Trimethyl Borate.
Veeraraghavan RP, et al.
Organic Letters, 14(24), 6119-6121 (2012)
R Meder et al.
Solid state nuclear magnetic resonance, 15(1), 69-72 (2000-07-21)
Boron-11 nuclear magnetic resonance imaging and spectroscopy have been used to characterise the nature and distribution of boron compounds after preservative treatment of radiata pine wood with trimethylborate (TMB). One day after treatment, 11B magnetic resonance imaging microscopy showed significant

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