288047
Triethyltin bromide
97%
Synonym(s):
Bromotriethylstannane
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About This Item
Linear Formula:
(C2H5)3SnBr
CAS Number:
Molecular Weight:
285.80
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
liquid
refractive index
n20/D 1.526 (lit.)
bp
222-224 °C (lit.)
density
1.63 g/mL at 25 °C (lit.)
SMILES string
CC[Sn](Br)(CC)CC
InChI
1S/3C2H5.BrH.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1
InChI key
KQPIFPBKXYBDGV-UHFFFAOYSA-M
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
Flash Point(F)
210.2 °F - closed cup
Flash Point(C)
99 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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J S Young et al.
Toxicology and applied pharmacology, 82(1), 87-93 (1986-01-01)
A single injection of trimethyltin chloride (TMT; 2, 4, or 6 mg/kg) is shown to produce a frequency-specific, dose-dependent auditory impairment, as well as to decrease the amplitude of the acoustically elicited startle response, in exposed rats. This finding stands
The effect of temperature on the inhibition of trout, carp and human red cell hexokinase by triethyltin bromide.
K R Siebenlist et al.
Comparative biochemistry and physiology. C: Comparative pharmacology, 70(2), 261-264 (1981-01-01)
G J Gerber et al.
Neurobehavioral toxicology and teratology, 7(5), 433-438 (1985-09-01)
Behavioral effects of triethyltin were studied in rats living in Wahmann activity cages. Wheel running activity and food-reinforced lever pressing were recorded 23 hr/day from 4 rats. Triethyltin injections (4 mg/kg IP) produced large transient decreases in running, lever pressing
S Yalçin et al.
Biochemical and biophysical research communications, 114(2), 829-834 (1983-07-29)
A set of inhibitors including hematin, bromosulfophthalein, and triethyltin bromide was used for discrimination and identification of the major basic isozymes of glutathione transferase in rat liver cytosol. Six enzymes are formed as binary combinations of 4 protein subunits: A
N Patritti-Laborde et al.
Enzyme, 35(2), 87-95 (1986-01-01)
Since organotin compounds represent an environmental health hazard, we determined the effect of triethyltin bromide (TTB) on red blood cell (RBC) enzyme activity. TTB produced a concentration-dependent inhibition of hexokinase and pyrimidine 5'-nucleotidase for both adult and cord RBC. D-Glucose
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