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288047

Sigma-Aldrich

Triethyltin bromide

97%

Synonym(s):

Bromotriethylstannane

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About This Item

Linear Formula:
(C2H5)3SnBr
CAS Number:
2767-54-6
Molecular Weight:
285.80
EC Number:
220-443-5
MDL number:
MFCD00000052
UNSPSC Code:
12352103
PubChem Substance ID:
24857311
NACRES:
NA.22

Quality Level

100

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
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H300 + H310 + H330,H410

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

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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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
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
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
B Veronesi et al.
Neurotoxicology, 7(1), 69-79 (1986-01-01)
Neuropathological and biochemical effects of neonatal exposure to the alkyl metal triethyltin were examined in juvenile male Long Evans rats. Rats were injected intraperitoneally on postnatal day 5 with 6 mg/kg of triethyltin bromide and sampled on day 20. The
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