Tin(IV) chloride solution

1.0 M in heptane

Stannic chloride, Tin tetrachloride
Linear Formula:
CAS Number:
Molecular Weight:
MDL number:
PubChem Substance ID:
Pricing and availability is not currently available.

Quality Level

reaction suitability

core: tin
reagent type: Lewis acid
reagent type: catalyst


1.0 M in heptane


0.874 g/mL at 25 °C

SMILES string




InChI key


Looking for similar products? Visit Product Comparison Guide

Signal Word


Hazard Codes


Risk Statement


Safety Statement



UN2924 - class 3 - PG 2 - EHS - acidic - Flammable liquids, corrosive, n.o.s., HI: all

WGK Germany


Flash Point(F)

24.8 °F - closed cup

Flash Point(C)

-4.0 °C - closed cup

Certificate of Analysis
Certificate of Origin
L Malaguarnera et al.
Journal of cellular biochemistry, 93(1), 197-206 (2004-09-08)
The pituitary hormone prolactin (PRL) is a multifunctional polypeptide which exerts a role on cell proliferation and may also contribute to cell differentiation. PRL is also produced by immune cells and is regarded as a key component of the neuroendocrine-immune...
Colin O'Brien et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(3), 902-909 (2006-11-07)
The reaction of silylated nucleophiles with 6,1-anhydroglucopyranuronic acid (glucuronic acid 6,1-lactones) catalysed by tin(IV) chloride provides 1,2-trans or 1,2-cis (deoxy)glycosides in a manner dependent on the donor structure. The alpha-glycoside was obtained for reactions of the donor with the 2-acyl...
Leo A Paquette et al.
The Journal of organic chemistry, 68(22), 8614-8624 (2003-10-25)
The concept of spirocyclic restriction, when generically applied to nucleoside mimics, allows for the preparation of diastereomeric pairs carrying either a syn- or anti-oriented hydroxyl at C-5'. Reported herein are convenient synthetic routes to enantiomerically pure 1-oxaspiro[4.4]nonanes featuring fully dihydroxylated...
Glycosidation reactions of silyl ethers with conformationally inverted donors derived from glucuronic acid: stereoselective synthesis of glycosides and 2-deoxyglycosides.
Monika Poláková et al.
Angewandte Chemie (International ed. in English), 43(19), 2518-2521 (2004-05-06)
Gary B Evans et al.
The Journal of organic chemistry, 69(6), 2217-2220 (2004-04-03)
Promotion by Lewis acid of the addition of some aryllithiums to a carbohydrate-based imine, which has allowed a more facile synthesis of some imino-C-nucleoside analogues, is described. Use of the corresponding nitrone does not assist in some cases, but lithiated...

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

Social Media

LinkedIn icon
Twitter icon
Facebook Icon
Instagram Icon


Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

© 2021 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.

Reproduction of any materials from the site is strictly forbidden without permission.