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Basic Information
CAS No.: 10026-06-9
Name: Stannic chloride pentahydrate
Article Data: 33
Molecular Structure:
Molecular Structure of 10026-06-9 (Stannic chloride pentahydrate)
Formula: SnCl4.5(H2O)
Molecular Weight: 368.614
Synonyms: Stannane,tetrachloro-, pentahydrate (9CI);Tin chloride (SnCl4), pentahydrate (8CI);Stannic tetrachloride pentahydrate;Tetrachlorostannane pentahydrate;Tin tetrachloride pentahydrate;Tin(IV)chloride pentahydrate;Tin(Ⅳ)chloride pentahydrate;
EINECS: 231-588-9
Density: 2.040
Melting Point: 56 °C
Boiling Point: 114.1 °C at 760 mmHg
Solubility: soluble in water
Appearance: white solid
Hazard Symbols: CorrosiveC
Risk Codes: 34-52/53
Safety: 26-36/37/39-45-7/8-61
Transport Information: UN 2440 8/PG 3
PSA: 46.15000
LogP: 2.05570
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Specification

This chemical is called Stannic chloride pentahydrate, and it's also named as Tin(IV) chloride, pentahydrate (1:4:5). With the molecular formula of SnCl4.5(H2O), its CAS registry number is 10026-06-9. Additionally, this chemical is soluble in water and ethanol. It may decompose in contacting with moisture or water. Keep it in the sealed container, away from the chlorine, pine oil, ethylene oxide and alkyl nitrates.

Other characteristics of the Stannic chloride pentahydrate can be summarised as followings: (1)ACD/LogP: 7.52; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 7.52; (4)ACD/LogD (pH 7.4): 7.52; (5)ACD/BCF (pH 5.5): 304368.94; (6)ACD/BCF (pH 7.4): 304368.94; (7)#H bond acceptors: 0; (8)#H bond donors: 0; (9)#Freely Rotating Bonds: 0; (10)Boiling Point: 114.1 °C at 760 mmHg; (11)Vapour Pressure: 23.9 mmHg at 25°C.

Production method of this chemical: Adding a small amount of 100g chloride anhydrous into 33mL water gradually, it's dissolved when heating. You get all the crystal from the transparent liquid under stirring and cooling. The Stannic chloride pentahydrate is 100 ~ 103 g and the yield is about 85 %.

Uses of this chemical: The Stannic chloride pentahydrate can serve as analytical reagent, mordant dyeing dehydrating agent in organic synthesis and textile mordant. It's also used for thin layer chromatography determination of triterpenes, steroids and phenols. Besides, it plays a role in organic synthesis, electronic industries.

You can still convert the following datas into molecular structure: 
1.SMILES: Cl[Sn](Cl)(Cl)Cl.O.O.O.O.O
2.InChI: InChI=1/4ClH.5H2O.Sn/h4*1H;5*1H2;/q;;;;;;;;;+4/p-4
3.InChIKey: KHMOASUYFVRATF-XBHQNQODAC

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 32mg/kg (32mg/kg)   U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02201,
rat LD50 intraperitoneal 120mg/kg (120mg/kg)   Acta Physiologica Polonica. Vol. 32, Pg. 719, 1981.