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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:
2767-54-6
Molecular Weight:
285.80
NACRES:
NA.22
PubChem Substance ID:
24857311
UNSPSC Code:
12352103
EC Number:
220-443-5
MDL number:
MFCD00000052

Key Documents

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Product Name

Triethyltin bromide, 97%

InChI key

KQPIFPBKXYBDGV-UHFFFAOYSA-M

InChI

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

SMILES string

CC[Sn](Br)(CC)CC

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.)

Quality Level

100

Related Categories

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

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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Certificates of Analysis (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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