Skip to Content
MilliporeSigma
All Photos(3)

Documents

31669

Sigma-Aldrich

Tin(II) chloride dihydrate

puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥98%

Synonym(s):

Stannous chloride dihydrate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
SnCl2 · 2H2O
CAS Number:
Molecular Weight:
225.65
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent
puriss. p.a.

Quality Level

agency

USP/NF
reag. ISO
reag. Ph. Eur.

assay

≥98%

form

fine crystals

impurities

≤0.002% ammonium (NH4)
≤0.005% insoluble in hydrochloric acid
≤0.01% other heavy metals (as Pb)
≤0.05% subst. not precip. by H2S (SO4)

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

anion traces

sulfate (SO42-): ≤20 mg/kg

cation traces

As: ≤1 mg/kg
Ca: ≤50 mg/kg
Cu: ≤10 mg/kg
Fe: ≤20 mg/kg
K: ≤50 mg/kg
Mg: ≤50 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤50 mg/kg

SMILES string

O.O.Cl[SnH2]Cl

InChI

1S/2ClH.2H2O.Sn/h2*1H;2*1H2;/q;;;;+2/p-2

InChI key

FWPIDFUJEMBDLS-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Tin(II) chloride dihydrate is the hydrated salt of tin(II). Its crystals are monoclinic and their structure has been investigated by single crystal X-ray diffraction method. Cell parameters were reported to be: a=9.313, b=7.250, c=8.970Å, β=114°55′ and Z=4.

Application

Tin(II) chloride dihydrate may be used in the following studies:
  • Synthesis of indoles.
  • Preparation of aldehydes.
  • As Lewis acid catalyst for the synthesis of 3-aminoimidazo[1,2-a]pyridines, via multi-component reactions.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Oral - STOT SE 3

target_organs

Cardio-vascular system, Respiratory system

Storage Class

8B - Non-combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 8

1 of 8

Tin(II) chloride anhydrous for synthesis

Sigma-Aldrich

8.18150

Tin(II) chloride

Tin(II) chloride ≥99.99% trace metals basis

Sigma-Aldrich

204722

Tin(II) chloride

ROCare Base cleaning chemical for removing organics, grime and slime from RO membranes

Milli-Q

ZWBASE012

ROCare

vibrant-m

BCR579

Coastal sea water (Hg)

Molybdic acid ≥85.0% MoO3 basis, ACS reagent

Sigma-Aldrich

232084

Molybdic acid

Hedieh Saffari et al.
Mayo Clinic proceedings, 95(3), 449-458 (2020-03-07)
To determine if heparin labeled with 99mTechnetium (99mTc) could be an imaging probe to detect eosinophil-related inflammation in eosinophilic esophagitis and to determine the biodistribution and radiation dosimetry of 99mTc-heparin oral administration using image-based dosimetry models with esophageal modeling. Freshly
An X-Ray Redetermination of the Crystal Structure of Tin (II) Chloride Dihydrate.
Kiriyama H, et al.
BuMed News Letter, 46(5), 1389-1395 (1979)
Anupam Bandyopadhyay et al.
Organic & biomolecular chemistry, 8(21), 4855-4860 (2010-08-25)
A facile synthetic route for the preparation of N-protected γ-amino β-keto esters from amino aldehydes and ethyl diazoacetate is described. The two component coupling is facilitated by tin(II) chloride followed by semipinacol rearrangement leading to the product in quantitative yield.
Tin (II) chloride dihydrate: A mild and efficient reagent for cleaving acetals.
Ford KL and Roskamp EJ.
Tetrahedron Letters, 33(9), 1135-1138 (1992)
Tin (II) Chloride Dihydrate Catalyzed Groebke Condensation: An Efficient Protocol for the Synthesis of 3-Aminoimidazo[1,2-a]pyridines.
Shaabani A, et al.
Chin. J. Chem., 27(2), 369-371 (2009)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service