Tin(II) chloride dihydrate

Name: Tin(II) chloride dihydrate
Brand: SIAL

suitable for AAS

Synonyme(s) :

Stannous chloride dihydrate

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About This Item

Formule linéaire :

SnCl₂ · 2H₂O

Numéro CAS:

10025-69-1

Poids moléculaire :

225.65

NACRES:

NA.21

PubChem Substance ID:

329770520

UNSPSC Code:

12352200

EC Number:

231-868-0

MDL number:

MFCD00149863

Nom du produit

Tin(II) chloride dihydrate, suitable for AAS

InChI key

FWPIDFUJEMBDLS-UHFFFAOYSA-L

InChI

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

SMILES string

O.O.Cl[SnH2]Cl

assay

≥96.0% (RT)

form

crystals

technique(s)

AAS: suitable

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

solubility

hydrochloric acid: passes test

anion traces

sulfate (SO₄^2-): ≤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

Quality Level

100

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Catégories apparentées

Chemistry & Biochemicals

Analytical Chemistry

Physical & Chemical Property Standards

Reference Materials

Tin (Sn)

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).

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.

pictograms

GHS08,GHS05,GHS07

signalword

Danger

hcodes

H290,H302 + H332,H314,H317,H335,H373,H412

pcodes

P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

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

Classe de stockage

8B - Non-combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificats d'analyse (COA)

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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)

Mercury speciation in thawed out and refrozen fish samples by gas chromatography coupled to inductively coupled plasma mass spectrometry and atomic fluorescence spectroscopy.

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

Room temperature sonolysis-based advanced oxidation process for degradation of organomercurials: application to determination of inorganic and total mercury in waters by flow injection-cold vapor atomic absorption spectrometry

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

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)

SnCl2-catalyzed selective atom economic imino Diels-Alder reaction: synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines.

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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