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Dimethyltin dichloride

HCID 12955
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
753-73-1
Standard SMILES
[CH3][Sn]([CH3])([Cl])[Cl]
InChIKey
PKKGKUDPKRTKLJ-UHFFFAOYSA-L
Molecular formula
C2H6Cl2Sn
Average molar mass
219.68 g/mol
Monoisotopic mass
219.886858

Overview

Dimethyltin dichloride is an organotin compound. Tin is a chemical element with the symbol Sn and atomic number 50. It is a natural component of the earth's crust and is obtained chiefly from the mineral cassiterite, where it occurs as tin dioxide. (L307, L309)

Names & identifiers

Preferred name
Dimethyltin dichloride
IUPAC
dichloro(dimethyl)stannane
English name
Dimethyltin dichloride
Molecular formula
C2H6Cl2Sn
Molecular weight
219.68

Names & synonyms

Dimethyltin dichloride753-73-1DichlorodimethyltinDichlorodimethylstannaneDimethyldichlorotinSTANNANE, DICHLORODIMETHYL-DimethyltindichlorideDimethyldichlorostannaneCotin 210Dichlorid dimethylcinicityDimethylzinndichlorideDTXSID5027304
Show more names
(CH3)2SnCl2DMTC50%SKL1117tin dichLTwo MethyltinDiMethyltin-di
DMTC7K42FNK7A0NSC-55159DTXCID907304RefChem:588622212-039-2dichloro(dimethyl)stannaneTin, dimethyl-, dichloride

Database identifiers

CAS
753-73-1
PubChem CID
12955
DTXSID
DTXSID5027304
UNII
7K42FNK7A0
EC Number
212-039-2

Properties

Computed structural properties

Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
0
Heavy atoms
5
Formal charge
0
Complexity
30.6

Experimental & physicochemical properties

Chemical ClassesMetals -> Tin Compounds, Organic
Vapor Pressure0.2 [mmHg]
Physical Description · 2 items

Wet Solid; Liquid

Produced as a solid or aqueous solution; [ECHA - Proposal for Harmonised Classification and Labelling] White crystalline solid; [Alfa Aesar MSDS]

Physicochemical properties

Melting point
101 · 101-106 °C (lit.)
Boiling point
188 · 188-190°C
Density
1 · 1,397 g/cm3
vapor pressure
4 Pa · 4Pa at 20℃
Flash point
185 · 185-190°C
storage temp.
2 · 2-8°C
solubility
0.1 g/mL, · methanol: 0.1 g/mL, clear
form
crystal
color
white
Specific Gravity
1.397 · 1.397

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Danger

H301: Toxic if swallowed [Danger Acute toxicity, oral]

P203, P260, P262, P264, P270, P271, P280, P284, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P318, P319, P320, P321, P330, P361+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)

Danger

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

P203, P260, P261, P262, P264, P264+P265, P270, P271, P273, P280, P284, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P318, P319, P320, P321, P330, P361+P364, P363, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 4 items

Chemical: Stannane, dichlorodimethyl-

Stannane, dichlorodimethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Stannane, dichlorodimethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: Dimethyltin dichloride (EC: 212-039-2)

Dimethyltin dichloride: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Stannane, dichlorodimethyl-: Human health tier II assessment
Hazards Summary · 1 item

Produced as a mixture with monomethyltin trichloride (CAS# 993-16-8); Teratogenicity observed in rats administered 20 mg/kg on days 7-17 of gestation; [Shepard's Catalog of Teratogenic Agents] Corrosive to rabbit skin; The nervous system is the target of toxicity in 90-day oral studies of rats, with neuropathological lesions observed in one study at doses as low as 25 ppm (1.6/2.2 mg/kg/day); One oral study of rats produced serious teratogenic effects not considered as related to maternal toxicity; Another study of rats demonstrated no teratogenicity; Possible developmental neurotoxicity observed in other studies of rats; [ECHA - Proposal for Harmonised Classification and Labelling] Reacts with water; Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; Toxic by ingestion, inhalation, and skin absorption; [Alfa Aesar MSDS] See Trimethyltin chloride and Di-n-butyltin dichloride. See Tin, organic compounds.

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 1 item

Though tin metal is very poorly absorbed, tin compounds may be absorbed via oral, inhalation, or dermal routes, with organotin compounds being much more readily absorbed than inorganic tin compounds. Tin may enter the bloodstream and bind to hemoglobin, where it is distributed and accumulates mainly in the kidney, liver, lung, and bone. Organotin compounds may undergo dealkylation, hydroxylation, dearylation, and oxidation catalyzed by cytochrome P-450 enzymes in the liver. The alkyl products of dealkylation are conjugated with glutathione and further metabolized to mercapturic acid derivatives. Tin and its metabolites are excreted mainly in the urine and feces. (L308)

Uses & manufacturing

Uses · 2 items

Used for stabilizing PVC potable water piping, making abrasion resistant glass containers, and as a catalyst for curing electrocoated paints; [Shepard's Catalog of Teratogenic Agents] Used to make other organotin compounds and for glass coating; [OECD: SIDS Dossier]

Painting (Pigments, Binders, and Biocides) [Category: Paint]

U.S. Production2023: 1,000,000 - <8,500,000 lb
Industry UsesIntermediate
General Manufacturing Information · 2 items

All Other Basic Organic Chemical Manufacturing

Stannane, dichlorodimethyl-: ACTIVE

Applications

UsesUsed as a pharmaceutical intermediate. It is employed as a coating, plastic and rubber auxilliary agent. Used as methyl Tin stabilizer intermediates, catalysts for esterification reaction, raw material for glass coating.

Upstream & downstream products

Downstream products

Related reactions

14 records
New reaction record
HRID 86193 reaction equation
HRID 86193As reactantTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 323912 reaction equation
HRID 323912As reactantuspto-grants-2001_04
HRID 461427 reaction equation
HRID 461427As reactantuspto-grants-1977_12
HRID 613794 reaction equation
HRID 613794As reactantuspto-grants-1999_12
HRID 908518 reaction equation
HRID 908518As reactantuspto-grants-2011_09
HRID 1086911 reaction equation
HRID 1086911As reactantuspto-grants-1991_07
HRID 1130162 reaction equation
HRID 1130162As reactantTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
HRID 1440432 reaction equation
HRID 1440432As reactantuspto-grants-1996_03
Page 1 of 2

Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Water Solubility
Slightly soluble in water (20 g/L (20°C)). Solubility in other solvents (0.1 g/ml in methanol).
Hydrolytic Sensitivity
0 · 0: forms stable aqueous solutions
Sensitive
Moisture Sensitive
BRN
3660508 · 3660508
Exposure limits
0.1 mg/m3; · ACGIH: TWA 0.1 mg/m3; STEL 0.2 mg/m3 (Skin)NIOSH: IDLH 25 mg/m3; TWA 0.1 mg/m3
Stability
Hygroscopic, Moisture sensitive
InChI
1S/2CH3.2ClH.Sn/h2*1H3;2*1H;/q;;;;+2/p-2
InChIKey
PKKGKUDPKRTKLJ-UHFFFAOYSA-L
SMILES
C[Sn](C)(Cl)Cl
LogP
-2.18 at · -2.18 at 22℃
CAS DataBase Reference
753 · 753-73-1(CAS DataBase Reference)
EWG's Food Scores
1 · 1
FDA UNII
7 K42FNK7A0 · 7K42FNK7A0
EPA Substance Registry System
Stannane, dichlorodimethyl- (753-73-1)
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
5 · GHS05,GHS06,GHS08
Signal word
Danger
Hazard statements
301 · H301+H311-H314-H330-H361d-H372-H412
Precautionary statements
260 · P260-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
target organs
Immune system,Nervous system
PPE
2 · Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes
T
Risk Statements
23 · 23/24/25-36/37/38-34
Safety Statements
26 · 26-36/37/39-45
RIDADR
2923 · UN 2923 8/PG 2
WGK Germany
3 · 3
RTECS
7245000 · WH7245000
TSCA
TSCA listed
HazardClass
6.1 · 6.1
PackingGroup
II
HS Code
29319090 · 29319090
Storage Class
6.1 A · 6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
Hazard Classifications
2 InhalationAcute · Acute Tox. 2 InhalationAcute Tox. 3 DermalAcute Tox. 3 OralAquatic Chronic 3Eye Dam. 1Repr. 2Skin Corr. 1BSTOT RE 1
REACH Registrations
Active
Hazard Classes and Categories · 3 items

Acute Tox. 3 (100%)

Acute toxicity (ingestion) - category 3

Repr. 2

Safety & protection

Exposure Control and Personal Protection0.02 [mg/m3], as Sn[German Research Foundation (DFG)]
Threshold Limit Values (TLV)0.2 [mg/m3], as Sn
Permissible Exposure Limit (PEL)0.1 [mg/m3], as Sn
Immediately Dangerous to Life or Health (IDLH)25.0 [mg/m3], as Sn

Toxicology

Health EffectsBreathing or swallowing, or skin contact with organotins, can interfere with the way the brain and nervous system work, causing death in severe cases. Organic tin compounds may also damage the immune and reproductive system. (L307, L308)
Adverse EffectsNeurotoxin - Other CNS neurotoxin
Exposure RoutesOral (L308) ; inhalation (L308) ; dermal (L308)
Toxicity Summary · 1 item

Organotin compounds produce neurotoxic and immunotoxic effects. Organotins may directly activate glial cells contributing to neuronal cell degeneration by local release of pro-inflammatory cytokines, tumor necrosis factor-_, and/or interleukins. They may also induce apoptosis by direct action on neuronal cells. Organotin compounds stimulate the neuronal release of and/or decrease of neuronal cell uptake of neurotransmitters in brain tissue, including aspartate, GABA, glutamate, norepinephrine, and serotonin. This may be either a contributing factor to or result of the neuronal cell loss. The immunotoxic effects of organotins are characterized by thymic atrophy caused by the suppression of proliferation of immature thymocytes and apoptosis of mature thymocytes. Organotin compounds are believed to exert these effects by suppressing DNA and protein synthesis, inducing the expression of genes involved in apoptosis (such as nur77), and disrupting the regulation of intracellular calcium levels, giving rise to the uncontrolled production of reactive oxygen species, release of cytochrome c to the cytosol, and the proteolytic and nucleolytic cascade of apoptosis. The suppression of proliferation of immature thymocytes further results in the suppression of T-cell-mediated immune responses. Organotins are also endocrine disruptors and are believed to contribute to obesity by inappropriate receptor activation, leading to adipocyte differentiation. Inorganic tin triggers eryptosis, contributing to tin-induced anemia. (L308, A182, A184)

Signs and SymptomsInorganic or organic tin compounds placed on the skin or in the eyes can produce skin and eye irritation. (L308)
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Toxicity DataLC50 (rat) = 115 mg/m3/4hr

Safety data

PPE
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
wgk
3
tsca
TSCA listed
rtecs
WH7245000
ridadr
UN 2923 8/PG 2
hs_code
29319090
risk_code
23/24/25-36/37/38-34
Signal word
Danger
Symbol(GHS)
GHS05,GHS06,GHS08
hazard_code
T
safety_code
26-36/37/39-45
hazard_class
6.1
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
packing_group
II
target organs
Immune system,Nervous system
Hazard statements
H301+H311-H314-H330-H361d-H372-H412
REACH Registrations
Active
Hazard Classifications
Acute Tox. 2 InhalationAcute Tox. 3 DermalAcute Tox. 3 OralAquatic Chronic 3Eye Dam. 1Repr. 2Skin Corr. 1BSTOT RE 1
Precautionary statements
P260-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Trimethyltin chlorideDimethyl tin dilaurate