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Merck

T48402

Sigma-Aldrich

2,2,2-Tribromoethanol

97%

Sinónimos:

Tribromoethyl alcohol

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About This Item

Fórmula lineal:
Br3CCH2OH
Número de CAS:
Peso molecular:
282.76
Beilstein/REAXYS Number:
1733249
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

bp

92-93 °C/10 mmHg (lit.)

mp

73-79 °C (lit.)

SMILES string

OCC(Br)(Br)Br

InChI

1S/C2H3Br3O/c3-2(4,5)1-6/h6H,1H2

InChI key

YFDSDPIBEUFTMI-UHFFFAOYSA-N

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General description

2,2,2-Tribromoethanol is generally used as an anesthetic drug for rodents.

Application

2,2,2-Tribromoethanol can be used as a functional initiator for the introduction of α-hydroxyl groups to poly(methyl methacrylate) and poly(n-butyl acrylate).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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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Xiangjie Sun et al.
Journal of virology, 90(23), 10936-10944 (2016-09-30)
Avian influenza A H7 viruses have caused multiple outbreaks in domestic poultry throughout North America, resulting in occasional infections of humans in close contact with affected birds. In early 2016, the presence of H7N8 highly pathogenic avian influenza (HPAI) viruses
Efficacy of Tribromoethanol.
Papaioannou VE & Fox JG
Laboratory Animal Science, 43(2) (1993)
R J Scott Lacombe et al.
Journal of lipid research, 58(10), 2071-2081 (2017-07-12)
DHA (22:6n-3) may be derived from two dietary sources, preformed dietary DHA or through synthesis from α-linolenic acid (ALA; 18:3n-3). However, conventional methods cannot distinguish between DHA derived from either source without the use of costly labeled tracers. In the
Emilio P Mottillo et al.
Molecular metabolism, 6(6), 471-481 (2017-06-06)
Fibroblast growth factor 21 (FGF21) shows great potential for the treatment of obesity and type 2 diabetes, as its long-acting analogue reduces body weight and improves lipid profiles of participants in clinical studies; however, the intracellular mechanisms mediating these effects
Chanyoung Song et al.
Nature communications, 10(1), 3745-3745 (2019-08-23)
The low response rate of current cancer immunotherapy suggests the presence of few antigen-specific T cells and a high number of immunosuppressive factors in tumor microenvironment (TME). Here, we develop a syringeable immunomodulatory multidomain nanogel (iGel) that overcomes the limitation

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