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288047

Sigma-Aldrich

Triethyltin bromide

97%

Sinônimo(s):

Bromotriethylstannane

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About This Item

Fórmula linear:
(C2H5)3SnBr
Número CAS:
2767-54-6
Peso molecular:
285.80
Número CE:
220-443-5
Número MDL:
MFCD00000052
Código UNSPSC:
12352103
ID de substância PubChem:
24857311
NACRES:
NA.22

Nível de qualidade

100

Ensaio

97%

forma

liquid

índice de refração

n20/D 1.526 (lit.)

pb

222-224 °C (lit.)

densidade

1.63 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC[Sn](Br)(CC)CC

InChI

1S/3C2H5.BrH.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1

chave InChI

KQPIFPBKXYBDGV-UHFFFAOYSA-M

Pictogramas

Skull and crossbonesEnvironment
GHS06,GHS09

Palavra indicadora

Danger

Frases de perigo

H300 + H310 + H330,H410

Classificações de perigo

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

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

210.2 °F - closed cup

Ponto de fulgor (°C)

99 °C - closed cup

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
MKCP8553
MKCN9618
MKCN4158
MKCN0647
MKCM6888

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W J Clerici et al.
Toxicology and applied pharmacology, 109(3), 547-556 (1991-07-11)
Two trialkyltin compounds, trimethyltin chloride (TMT) and triethyltin bromide (TET) were evaluated for their acute effects on cochlear function in pigmented guinea pigs. Compound action potential (CAP) thresholds and 1 microV RMS cochlear microphonic (CM) isopotential curves were generated for
P H Ruppert et al.
Neurotoxicology, 5(4), 9-22 (1984-01-01)
Triethyltin (TET) has been shown to be neurotoxic when injected on postnatal day (PND) 5. In the present experiment we examined the toxicity of a single exposure to TET at several postnatal ages. Rat pups were injected ip with 0
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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