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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
Assay:
97%
Form:
liquid

Key Documents

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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

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

2767-54-6

CAS No.

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ5924
MKCZ3148
MKCV8575
MKCV5052
MKCP8553

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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
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
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
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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