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7772-99-8 molecular structure
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tin(2+) ion dichloride

ChemBase ID: 105846
Molecular Formular: Cl2Sn
Molecular Mass: 189.607
Monoisotopic Mass: 189.83989936
SMILES and InChIs

SMILES:
[Cl-].[Cl-].[Sn+2]
Canonical SMILES:
[Cl-].[Cl-].[Sn+2]
InChI:
InChI=1S/2ClH.Sn/h2*1H;/q;;+2/p-2
InChIKey:
AXZWODMDQAVCJE-UHFFFAOYSA-L

Cite this record

CBID:105846 http://www.chembase.cn/molecule-105846.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
tin(2+) ion dichloride
λ2-tin(2+) ion dichloride
IUPAC Traditional name
tin, ion (sn2+) dichloride
λ2-tin(2+) ion dichloride
Synonyms
Stannous chloride, anhydrous
Tin(II) chloride, anhydrous
Stannous chloride
Tin(II) chloride, ultra dry
Stannous chloride dihydrate
Tin(II) chloride dihydrate
Tin (II) Chloride
Tin Dichloride
Tin Protochloride
STANNOUS CHLORIDE DIHYDRATE
Tin(II) chloride solution
Tin standard solution
无水氯化锡 (II)
氯化锡 (II), 超干
氯化锡 (II), 无水
氯化锡(II)二水合物
Tin standard solution
CAS Number
7772-99-8
10025-69-1
EC Number
231-868-0
231-141-8
MDL Number
MFCD00149863
MFCD00133862
MFCD00011241
Merck Index
148783
PubChem SID
162086862
PubChem CID
5284466

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa -7.0  H Acceptors
H Donor LogD (pH = 5.5) 0.8327582 
LogD (pH = 7.4) 0.8327582  Log P 0.6123387 
Molar Refractivity 5.6156 cm3 Polarizability 2.1090326 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
Soluble in water, alkalies, alcohol, MEK, methyl acetate, ether, and acetone expand Show data source
Apperance
Crystalline expand Show data source
Powder, Ampouled under argon expand Show data source
Melting Point
231.9 °C expand Show data source
247°C expand Show data source
42-46°C expand Show data source
Boiling Point
2260 °C at 1013 hPa expand Show data source
652°C expand Show data source
Density
2.71 expand Show data source
3.95 expand Show data source
7.3 g/cm3 at 20 °C expand Show data source
Vapor Pressure
1.3332 hPa at 1492 °C expand Show data source
Storage Condition
Room Temperature (15-30°C), Store Under Nitrogen expand Show data source
Storage Warning
Air Sensitive & Hygroscopic expand Show data source
RTECS
XP8700000 expand Show data source
XP8850000 expand Show data source
European Hazard Symbols
Corrosive Corrosive (C) expand Show data source
X expand Show data source
UN Number
1759 expand Show data source
UN3260 expand Show data source
MSDS Link
Download expand Show data source
Hazard Class
8 expand Show data source
Packing Group
II expand Show data source
III expand Show data source
Australian Hazchem
2X expand Show data source
Risk Statements
22-34-43 expand Show data source
34 expand Show data source
R:34 expand Show data source
Safety Statements
20-26-36/37/39-45-60 expand Show data source
24-26-36/37/39-45 expand Show data source
26-36/37/39-45 expand Show data source
S:26-27/28-36/37/39-46-64 expand Show data source
EU Classification
C10 expand Show data source
EU Hazard Identification Number
8B expand Show data source
Emergency Response Guidebook(ERG) Number
154 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS07 expand Show data source
GHS Hazard statements
H314-H318-H302-H317 expand Show data source
H314-H318-H303 expand Show data source
GHS Precautionary statements
P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A expand Show data source
P280-P262-P305+P351+P338-P309-P310 expand Show data source
Purity
98% expand Show data source
99% min expand Show data source
99.9985% (metals basis) expand Show data source
Concentration
1 mg/mL Sn expand Show data source
1000 ppm Sn expand Show data source
Certificate of Analysis
Download expand Show data source
Suitability
suitable for atomic absorption spectrometry expand Show data source
Empirical Formula (Hill Notation)
SnCl2 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals
MP Biomedicals - 02194744 external link
Cell Culture Reagent
Dihydrate

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • For applications see under dihydrate.
  • • Nitro aromatics can be selectively reduced in the presence of aldehyde, nitrile or halogen substituents, using ethanol - ethyl acetate as solvent: Tetrahedron Lett., 25, 839 (1984). ɑ?-Unsaturated nitro compounds are reduced to the oximes of saturated ketones: Synth. Commun., 18, 693 (1988).
  • • For use in the preparation of aldehydes by the Stephen reduction of aromatic nitriles, see: Org. Synth. Coll., 3, 626 (1955), and by the Sonn-Mueller reduction of imidoyl chlorides: Org. Synth. Coll., 3, 818 (1955).
  • • Catalyzes the reaction of ethyl diazoacetate with aldehydes to give ?-keto esters: J. Org. Chem., 54, 3258 (1989). For carbon-carbon double-bond formation between ɑ-halo ketones and aldehydes, mediated by SnCl2/Na2SO3, see: Synth. Commun., 23, 271 (1993).
  • • Reduces azides to amines in methanol: Tetrahedron Lett., 27, 1425 (1986).
  • • Catalyst for tetrahydropyranylation of alcohols: Synth. Commun., 29, 1679 (1999).
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PATENTS

PATENTS

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INTERNET

INTERNET

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