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T48402

Sigma-Aldrich

2,2,2-Tribromoethanol

97%

Synonym(s):

Tribromoethyl alcohol

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About This Item

Linear Formula:
Br3CCH2OH
CAS Number:
75-80-9
Molecular Weight:
282.76
Beilstein:
1733249
EC Number:
200-903-1
MDL number:
MFCD00004671
UNSPSC Code:
12352100
PubChem Substance ID:
24900231
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).

Other Notes

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Efficacy of Tribromoethanol.
Papaioannou VE & Fox JG
Laboratory Animal Science, 43(2) (1993)
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Clinical trials with autologous adipose-derived stem cell (AdSC) therapy for ischemic heart diseases (IHDs) are ongoing. However, little is known about combinational therapeutic effect of AdSCs and statin poly(lactic-co-glycolic) acid (PLGA) nanoparticles on the ischemic myocardium. We investigated the hypothesis
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
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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
Radika Soysa et al.
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