T48402
2,2,2-Tribromoethanol
97%
Synonym(s):
Tribromoethyl alcohol
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About This Item
Linear Formula:
Br3CCH2OH
CAS Number:
Molecular Weight:
282.76
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-903-1
Beilstein/REAXYS Number:
1733249
MDL number:
Assay:
97%
Quality Level
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
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).
signalword
Warning
hcodes
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Efficacy of Tribromoethanol.
Papaioannou VE & Fox JG
Laboratory Animal Science, 43(2) (1993)