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7646-78-8 molecular structure
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tetrachlorostannane

ChemBase ID: 129918
Molecular Formular: Cl4Sn
Molecular Mass: 260.513
Monoisotopic Mass: 259.77760472
SMILES and InChIs

SMILES:
Cl[Sn](Cl)(Cl)Cl
Canonical SMILES:
Cl[Sn](Cl)(Cl)Cl
InChI:
InChI=1S/4ClH.Sn/h4*1H;/q;;;;+4/p-4
InChIKey:
HPGGPRDJHPYFRM-UHFFFAOYSA-J

Cite this record

CBID:129918 http://www.chembase.cn/molecule-129918.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
tetrachlorostannane
IUPAC Traditional name
tin(IV) chloride
Synonyms
Stannic chloride fuming
Tin(IV) chloride
Tin tetrachloride
Tin(IV) chloride solution
Stannic chloride
Tin(IV) chloride
Tin(IV) chloride, anhydrous
发烟氯化高锡
四氯化锡
四氯化锡
氯化高锡
氯化锡(IV) 溶液
四氯化锡(IV), 无水
CAS Number
7646-78-8
EC Number
231-588-9
MDL Number
MFCD00011242
Merck Index
148774
PubChem SID
24855025
24852219
162224204
24853039
24861921
PubChem CID
24287
Chemspider ID
22707
Wikipedia Title
Tin(IV)_chloride

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) -2.962  LogD (pH = 7.4) -2.962 
Log P -2.962  Molar Refractivity 24.5452 cm3
Polarizability 14.503247 Å3 Polar Surface Area 0.0 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
decomposes (anhydrous)
very soluble (pentahydrate) in water
expand Show data source
soluble in alcohol, benzene, toluene, chloroform, acetone, kerosene, CCl4, methanol expand Show data source
Soluble in alcohol, CCl4, benzene, toluene, and acetone. Soluble in water with much heat evolution expand Show data source
Apperance
colorless fuming liquid expand Show data source
Liquid expand Show data source
Melting Point
-33 °C(lit.) expand Show data source
-33°C expand Show data source
-33°C expand Show data source
Boiling Point
114 °C(lit.) expand Show data source
114.15°C expand Show data source
114°C expand Show data source
Flash Point
1 °C expand Show data source
34 °F expand Show data source
Density
0.874 g/mL at 25 °C expand Show data source
1.419 g/mL at 25 °C expand Show data source
1.44 g/mL at 20 °C expand Show data source
2.217 g/mL at 20 °C(lit.) expand Show data source
2.226 g/ml (anhydrous)
2.04 g/cm3 (pentahydrate)
expand Show data source
2.226 g/mL at 25 °C(lit.) expand Show data source
2.26 expand Show data source
Refractive Index
1.512 expand Show data source
Vapor Pressure
10 mmHg ( 10 °C) expand Show data source
18.6 mmHg ( 20 °C) expand Show data source
20 mmHg ( 22 °C) expand Show data source
Vapor Density
9 (vs air) expand Show data source
Storage Warning
Moisture Sensitive expand Show data source
RTECS
XP8750000 expand Show data source
European Hazard Symbols
Corrosive Corrosive (C) expand Show data source
Flammable Flammable (F) expand Show data source
Toxic Toxic (T) expand Show data source
UN Number
1827 expand Show data source
2924 expand Show data source
3264 expand Show data source
UN1827 expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Hazard Class
3 expand Show data source
8 expand Show data source
Packing Group
2 expand Show data source
II expand Show data source
Risk Statements
11-23/24/25-34 expand Show data source
34-40-52/53 expand Show data source
34-52/53 expand Show data source
R34, R52/53 expand Show data source
Safety Statements
16-26-36/37/39-45 expand Show data source
26-36/37/39-45-61 expand Show data source
7/8-26-45-61 expand Show data source
S1/2, S7/8, S26, S45, S61 expand Show data source
TSCA Listed
expand Show data source
EU Index
050-001-00-5 expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS07 expand Show data source
GHS08 expand Show data source
GHS Signal Word
Danger expand Show data source
NFPA704
NFPA 704 diagram
0
3
1
expand Show data source
GHS Hazard statements
H314-H318-H402-H412 expand Show data source
H314-H335-H351-H412 expand Show data source
H314-H335-H412 expand Show data source
H314-H412 expand Show data source
GHS Precautionary statements
P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A expand Show data source
P261-P273-P280-P305 + P351 + P338-P310 expand Show data source
P273-P280-P305 + P351 + P338-P310 expand Show data source
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter expand Show data source
RID/ADR
UN 1827 8/PG 2 expand Show data source
UN 2924 3/PG 2 expand Show data source
UN 3264 8/PG 2 expand Show data source
Purity
≥99% expand Show data source
98% (metals basis) expand Show data source
99% expand Show data source
99.995% expand Show data source
Concentration
~1 M in methylene chloride expand Show data source
1.0 M in heptane expand Show data source
1.0 M in methylene chloride expand Show data source
Grade
purum expand Show data source
Cation Traces
As: ≤50 mg/kg expand Show data source
Fe: ≤10 mg/kg expand Show data source
Antion Traces
sulfate (SO42-): ≤100 mg/kg expand Show data source
Linear Formula
SnCl4 expand Show data source

DETAILS

DETAILS

Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 217913 external link
Application
Doping polyaniline, an intensively studied polymer, with SnCl4 stabilizes its solution in nitromethane and allows solution processing.1
Lewis acid catalyst
Packaging
5, 25, 100 g in glass bottle
Sigma Aldrich - 249955 external link
Packaging
4×25, 100, 800 mL in Sure/Seal™
Sigma Aldrich - 357499 external link
Packaging
100 mL in Sure/Seal™
Sigma Aldrich - 208930 external link
Packaging
2 kg in Sure/Seal™
250 g in Sure/Seal™

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Lewis acid catalyst, e.g. for intermolecular: Org. Synth. Coll., 2, 8 (1943), or intramolecular: Org. Synth. Coll., 4, 900 (1963) Friedel-Crafts acylations.
  • • Mediates condensations with silyl enol ethers, see, e.g.: Org. Synth. Coll., 7, 414 (1990); 8, 578 (1993).
  • • In the presence of tri-n-butylamine, reacts with terminal alkynes to give reactive alkynyltrichlorotin reagents, which effect alkynylation of aldehydes, acetals and enones: Chem. Lett., 2479 (1992).
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PATENTS

PATENTS

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INTERNET

INTERNET

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