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Merck

288047

Triethyltin bromide

97%

Synonym(s):

Bromotriethylstannane

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About This Item

Linear Formula:
(C2H5)3SnBr
CAS Number:
Molecular Weight:
285.80
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
220-443-5
MDL number:
Assay:
97%
Form:
liquid
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Quality Level

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

pictograms

Skull and crossbonesEnvironment

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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L W Reiter et al.
Neurobehavioral toxicology and teratology, 3(3), 285-293 (1981-01-01)
On Day 5 of postnatal life, rat pups received a single injection of triethyltin and were later tested for a variety of developmental and adult behaviors. A within-litter dosing design was used with one male and one female from each
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
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
K R Siebenlist et al.
The Journal of biological chemistry, 258(18), 11384-11390 (1983-09-25)
Triethyltin bromide activates the cyclic AMP-dependent protein kinases of human red cell membranes and of bovine brain. Additions of 25-500 microM triethyltin to red cell ghosts resulted in enhanced phosphorylation of ghost proteins. When added to partially purified cyclic AMP-dependent
M K Tahir et al.
The Journal of biological chemistry, 261(3), 1048-1051 (1986-01-25)
Simple inhibition studies in which fractional velocity is measured as a function of inhibitor concentration were used to distinguish heterodimeric from homodimeric isoenzymes of glutathione transferase. Homodimeric isoenzymes from rat, mouse, and human tissues were shown to give graphs of

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