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96527

Supelco

Tin(II) chloride dihydrate

suitable for AAS

Synonym(s):

Stannous chloride dihydrate

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About This Item

Linear Formula:
SnCl2 · 2H2O
CAS Number:
10025-69-1
Molecular Weight:
225.65
EC Number:
231-868-0
MDL number:
MFCD00149863
UNSPSC Code:
12000000
PubChem Substance ID:
329770520
NACRES:
NA.21

Assay

≥96.0% (RT)

Quality Level

100

form

crystals

technique(s)

AAS: suitable

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

solubility

hydrochloric acid: passes test

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
Hg: ≤5 μg/kg
K: ≤50 mg/kg
NH4+: ≤10 mg/kg
Na: ≤100 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

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General description

Tin(II) chloride dehydrate converts conjugated dioxolones to aldehyde. It helps as a catalyst in multi-component condensation reaction from aromatic aldehydes, 2-aminopyridines and isonitriles which results in reasonable yield and reducing the reaction time.

Application

Tin(II) chloride dehydrate may be used:
  • As a reducing agent for the determination of hydride forming species by AAS.
  • In the conversion of organomercurials into inorganic mercury determined using a flow injection-cold vapor atomic absorption spectrometry
  • In the determination of total mercury content, using atomic fluorescence spectroscopy and mercury speciation was performed using gas chromatography inductively coupled plasma mass spectrometry (GC-ICPMS).

Signal Word

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 Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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.

PDSCL

Deleterious substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

96527-50G:4548173341552
96527-VAR:
96527-BULK:
96527-250G:4548173341569

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM1811
BCCM5040
BCCJ8320
BCCL1521
BCCH9912

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Petra Krystek et al.
Analytical and bioanalytical chemistry, 381(2), 354-359 (2004-08-05)
Different sub-sampling procedures were applied for the determination of mercury species (as total mercury Hg, methylmercury MeHg+ and inorganic mercury Hg2+) in frozen fish meat. Analyses were carried out by two different techniques. After the sample material was pre-treated by
Tin (II) Chloride Dihydrate Catalyzed Groebke Condensation: An Efficient Protocol for the Synthesis of 3-Aminoimidazo [1, 2-a] pyridines.
Shaabani, Ahmad, et al.
Chin. J. Chem., 27, 369-371 (2009)
Tin (II) chloride dihydrate: A mild and efficient reagent for cleaving acetals.
Ford, Kelley L., and Eric J. Roskamp
Tetrahedron Letters, 33, 1135-1138 (1992)
Capelo et al.
Analytical chemistry, 72(20), 4979-4984 (2000-10-31)
A new oxidation method based on room-temperature ultrasonic irradiation (sonolysis) is proposed for conversion of organomercurials into inorganic mercury and subsequent determination by flow injection-cold vapor atomic absorption spectrometry. This advanced oxidation process eliminates the need for chemical oxidants, high
Rajendran Suresh et al.
The Journal of organic chemistry, 77(3), 1468-1476 (2012-01-11)
The synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines by a SnCl(2)-catalyzed multicomponent reaction has been described. The reaction proceeds chemo- and regioselectively in an atom-economic way, generating a library of 24 quinoline derivatives.
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