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Bis(acetato)dibutylzinn

Dibutyltin diacetate

HCID 16682740
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GrundinformationenNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
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Grundinformationen

CAS
1067-33-0
Standard-SMILES
CCC[CH2][Sn]([CH2]CCC)([O]C(C)=O)[O]C(C)=O
InChIKey
JJLKTTCRRLHVGL-UHFFFAOYSA-L
Summenformel
C12H24O4Sn
Durchschnittliche Molmasse
351,03 g/mol
Monoisotopische Masse
352,069662

Namen und Bezeichner

Bevorzugter Name
Dibutyltin diacetate
IUPAC
[acetyloxy(dibutyl)stannyl] acetate
Lokaler Name
Bis(acetato)dibutylzinn
Englischer Name
bis(acetato)dibutyltin
Summenformel
C12H24O4Sn
Molmasse
351.02656

Namen und Synonyme

DIBUTYLTIN DIACETATE1067-33-0DiacetoxybutyltinDiacetoxydibutyltinDiacetoxydibutylstannaneStannane, bis(acetyloxy)dibutyl-Di-n-butyltin diacetateBis(acetyloxy)dibutylstannaneT 1 (Catalyst)Stannane, diacetoxydibutyl-Dibutylstannium diacetateFomrez sul-3
Weitere Namen anzeigen
bis(acetato)dibutyltin
DiacetoxydibutlyltinDibutyl tin diacetateDibutyltin di(acetate)Dibutyltin acetateTin, dibutyl-, diacetateBA 2726NCI-C02028Dibutyldiacetoxystannane

Datenbank-Bezeichner

CAS
1067-33-0、17523-06-7
PubChem CID
16682740
DTXSID
DTXSID3020419
UNII
BC9AZH1UZG
EC Number
213-928-8、241-521-5

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

Polarare Oberfläche (TPSA)
52,6 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
4
Frei drehbare Bindungen
10
Schwere Atome
17
Formalladung
0
Komplexität
227

Experimentelle und physikochemische Eigenschaften

LogPlog Kow=1.27
OdorSlight acetic acid
Density · 3 Einträge

1.31 at 77 °F (NTP, 1992) - Denser than water; will sink

1.31 at 25 °C

1.31 @25 °C

Viscosity18 cP at 25 °C
Color/Form · 2 Einträge

COLORLESS LIQUID

Clear, yellow liquid

Solubility · 2 Einträge

less than 1 mg/mL at 59 °F; forms white precipitate (NTP, 1992)

Sol in water and most org solvents

Flash Point · 2 Einträge

290 °F (NTP, 1992)

143 °C (290 °F) (OPEN CUP)

Boiling Point · 3 Einträge

266 °F at 2 mmHg (NTP, 1992)

130 °C @ 2 mm Hg

130 °C @760 [mm Hg]

DecompositionWhen heated to decomposition, it emits acrid smoke & irritating fumes.

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H341: Suspected of causing genetic defects [Warning Germ cell mutagenicity];H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity];H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure]

P203, P260, P264, P270, P280, P318, P319, P405, and P501 (click each P-code to see the statement)

This chemical does not meet GHS hazard criteria for 1.5% (10 of 665) of reports.

Gefahrenhinweise

Regulatory Information · 5 Einträge

Chemical: Stannane, bis(acetyloxy)dibutyl-

Hazard Traits - Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B;Report - if used as a fragrance or flavor ingredient

Acetic acid, 1,1'-(dibutylstannylene) ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, 1,1'-(dibutylstannylene) ester 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)

Status: Active Update: 30-06-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/13153

Dibutyltin diacetate: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Stannane, bis(acetyloxy)dibutyl-: Human health tier II assessment
DOT LabelPoison
Fire HazardsThis chemical is combustible. (NTP, 1992)
Fire PotentialCombustible when exposed to heat or flame; can react with oxidizing materials.

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 3 Einträge

DIBUTYLTIN DIACETATE UNDERGOES MONOOXYGENASE OR NONENZYMATIC CLEAVAGE TO BUTYLTIN DERIVATIVES. SEVERAL OF METABOLITES FORMED IN MICROSOMAL MONOOXYGENASE SYSTEM ARE DETECTED IN LIVER & FECES OF MICE ORALLY ADMIN DIBUTYLTIN DIACETATE.

Dibutyltin diacetate yielded butyltin derivatives under the reaction conditions used. Several of the metabolites that were produced in vitro were also found in the liver or feces of mice exposed to tributyltin acetate or dibutyltin diacetate by gavage. In the isolated rat liver microsome system, other trialkyltin compounds, including the ethyl, propyl, pentyl, hexyl and cyclohexyl derivatives, appeared to undergo analogous monooxygenase reactions.

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)

Verwendung und Herstellung

Uses · 6 Einträge

Used as stabilizer for polyvinyl chloride, a catalyst for manufacturing silicone and urethane foams, and a curing agent for silicone elastomers; [HSDB]

Plastic Composites Manufacturing [Category: Industry]

Stabilizer for chlorinated org cmpd; catalyst for condensation reactions.

CATALYST FOR MFR OF SILICONE AND URETHANE FOAMS, FOR ESTERIFICATION REACTIONS

The largest single industrial application for organotin compounds is in the stabilization of polyvinyl chloride. /Diorganotin compounds/

Dialkyltin compounds are the best general-purpose stabilizers for polyvinyl chloride, esp if colorlessness & transparency are required. ... Diorganotin compounds have been used increasingly as catalysts for high resiliency foam in automotive seating. /Diorganotin compounds/

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Reaktionsgleichung von HRID 185943
HRID 185943als EduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaktionsgleichung von HRID 1678541
HRID 1678541als Eduktuspto-grants-2011_08
Reaktionsgleichung von HRID 2112982
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Auf dieser SeiteGrundinformationenNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
Melting Point · 2 Einträge

less than 53.6 °F (NTP, 1992)

10 °C

Vapor Density · 2 Einträge

12.1 (NTP, 1992) - Heavier than air; will sink (Relative to Air)

12.1 (Air = 1)

Vapor Pressure · 3 Einträge

1.3 [mmHg]

1.3 mm Hg at 20 °C

1.3 [mm Hg] @20 °C

Health HazardsSYMPTOMS: This compound may cause skin rashes after contact.;ACUTE/CHRONIC HAZARDS: This compound can be absorbed through the skin and can cause skin rashes following contact. (NTP, 1992)
Hazards SummaryRats given 1/4 the LD50 dose daily for 10 days developed signs of hepatotoxicity; Oral LD50 (rat) = 32 mg/kg; [HSDB] May cause skin rashes; Can be absorbed through skin; [CAMEO] An irritant; [MSDSonline] See Tin, organic compounds.
Reactive GroupSalts, Basic;Organometallics
Reactivity Profile · 1 Eintrag

DIBUTYLTIN DIACETATE is stable under normal laboratory conditions. This compound may react with oxidizers. (NTP, 1992). Strongly reactive with many other groups. Incompatible with acids and bases. Organometallics are good reducing agents and therefore incompatible with oxidizing agents.

Air and Water ReactionsForms white precipitate in water. Insoluble in water.
Hazard Classes and Categories · 4 Einträge

Skin Corr. 1B (94.7%);Skin Sens. 1 (82%);Eye Dam. 1 (76.5%);Muta. 2 (82.4%);Repr. 1B (64.4%);Repr. 1B (18.2%);STOT SE 1 (82%);STOT RE 1 (92.3%);Aquatic Acute 1 (58.6%);Aquatic Chronic 1 (89%)

Germ cell mutagenicity - category 2;Skin corrosion - category 1;Specific target organ toxicity (repeated exposure) - category 1;Reproductive toxicity - category 1B

Acute toxicity (Oral) - Category 2;Reproductive toxicity - Category 1B;Specific target organ toxicity - Repeated exposure - Category 2 (liver);Hazardous to the aquatic environment (Acute) - Category 1;Hazardous to the aquatic environment (Long-term) - Category 1

Muta. 2;Repr. 1B;STOT RE 1

State Drinking Water Guidelines(MN) MINNESOTA 4000 ug/l /Tin/

Sicherheit und Schutzausrüstung

Fire FightingFires involving this compound should be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.;SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. IMMEDIATELY call a hospital or poison control center even if no symptoms (such as redness or irritation) develop. IMMEDIATELY transport the victim to a hospital for treatment after washing the affected areas.;INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.;INGESTION: Some heavy metals are VERY TOXIC POISONS, especially if their salts are very soluble in water (e.g., lead, chromium, mercury, bismuth, osmium, and arsenic). IMMEDIATELY call a hospital or poison control center and locate activated charcoal, egg whites, or milk in case the medical advisor recommends administering one of them. Also locate Ipecac syrup or a glass of salt water in case the medical advisor recommends inducing vomiting. Usually, this is NOT RECOMMENDED outside of a physician's care. If advice from a physician is not readily available and the victim is conscious and not convulsing, give the victim a glass of activated charcoal slurry in water or, if this is not available, a glass of milk, or beaten egg whites and IMMEDIATELY transport victim to a hospital. If the victim is convulsing or unconscious, do not give anything by mouth, assure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

Exposure Control and Personal Protection0.02 [mg/m3], inhalable fraction, as Sn[German Research Foundation (DFG)]
Fire Fighting ProceduresTo fight fire use water, foam, carbon dioxide, dry chemical.
Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If you spill this chemical, use absorbent paper to pick up all liquid spill material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.;STORAGE PRECAUTIONS: You should store this material in a refrigerator. (NTP, 1992)

Disposal Methods · 1 Eintrag

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Preventive Measures · 2 Einträge

Clothing contaminated with ... dibutyltin diacetate ... should be placed in closed containers for storage until it can be discarded or until provision is made for the removal of contaminant from the clothing. If the clothing is to be laundered or otherwise cleaned to remove the contaminant, the person performing the operation should be informed of contaminant's hazard properties. ... Non-impervious clothing which becomes contaminated with ... dibutyltin diacetate ... should be removed promptly & not reworn until the contaminant is removed.

Skin that becomes contaminated with ... dibutyltin diacetate ... should be promptly washed or showered with soap or mild detergent & water to remove any contaminant. ... Eating & smoking should not be permitted in areas where ... dibutyltin diacetate ... is handled, processed, or stored.

Isolation and Evacuation · 1 Eintrag

Excerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:;IMMEDIATE PRECAUTIONARY MEASURE: Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.;SPILL: Increase the immediate precautionary measure distance, in the downwind direction, as necessary.;FIRE: If tank, rail tank car or highway tank is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2024)

Threshold Limit Values (TLV) · 4 Einträge

0.1 [mg/m3], as Sn

0.2 [mg/m3], as Sn

8 hr Time Weighted Avg (TWA): 0.1 mg/cu m; 15 min Short Term Exposure Limit (STEL): 0.2 mg/cu m. Skin. /Tin, organic compounds, as Sn/

A4; Not classifiable as a human carcinogen. /Tin, organic compounds, as Sn/

Permissible Exposure Limit (PEL)0.1 [mg/m3], as Sn
Protective Action Criteria (PAC) · 3 Einträge

0.009 [mg/m3]

1.1 [mg/m3]

6.3 [mg/m3]

Personal Protective Equipment (PPE) · 2 Einträge

MINIMUM PROTECTIVE CLOTHING: If Tyvek-type disposable protective clothing is not worn during handling of this chemical, wear disposable Tyvek-type sleeves taped to your gloves.;RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Employees should be provided with & required to use impervious clothing, gloves, face shields (8 inch minimum), & other appropriate protective clothing necessary to prevent repeated or prolonged skin contact with ... solid or liquid dibutyltin diacetate. ... Employees should be provided with & required to use dust- & splash-proof safety goggles where solid or liquid dibutyltin diacetate ... may contact the eyes.

Toxikologische Informationen

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 Effects · 1 Eintrag

Neurotoxin - Other CNS neurotoxin;Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.;ACGIH Carcinogen - Not Classifiable.

Exposure RoutesOral (L308) ; inhalation (L308) ; dermal (L308)
Toxicity Summary · 1 Eintrag

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)
Ongoing Test Status · 1 Eintrag

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=1067-33-0]

Carcinogen Classification · 6 Einträge

Dibutyltin diacetate

TR-183: Bioassay of Dibutyltin Diacetate for Possible Carcinogenicity (CASRN 1067-33-0) (1979 )

10/25/78

No Evidence

Inadequate Experiment

No Evidence

Non-Human Toxicity Excerpts · 4 Einträge

... THE EFFECT OF DIBUTYLTIN DIACETATE ON THE ULTRASTRUCTURE OF MOUSE LIVER /WAS STUDIED/. IN THIS STUDY, RATS WERE GIVEN ORALLY 1/4 LD50 DOSE /110 MG/KG/ DAILY FOR 10 DAYS. ONE RAT WAS SACRIFICED EACH DAY & THE LIVER TISSUE REMOVED FOR ... LIGHT & ELECTRON MICROSCOPY. WITHIN 2-3 DAY PERIOD, PATHOLOGIC FEATURES WERE OBSERVED, INDICATING THAT THE ... /CHEM/ WAS ACTING AS A HEPATOTOXIC AGENT. CHANGES IN THE ULTRASTRUCTURE OF LIVER CELLS WERE EVIDENT & EARLY MITOCHONDRIAL DAMAGE WAS OBSERVED. SWELLING OF GRANULAR & AGRANULAR ENDOPLASMIC RETICULUM FOLLOWED SOON AFTER THE MITOCHONDRIAL CHANGES WERE NOTED. PROGRESSIVE CONGESTION OF BILE CANALICULI OCCURRED, DUE IN PART TO CELLULAR & MICROVILLI SWELLING.

Dibutyltin diacetate was evaluated for the induction of sex-linked recessive lethal mutations in Drosophila melanogaster by the National Toxicology Program. Canton-S wild-type males were treated with concentrations of dibultyltin diacetate that result in approximately 30% mortality. Following treatment, males were mated individually to 3 harems of Basc virgin females to produce 3 broods for analysis. The concentrations of dibutyltin diacetate tested by injection (150 ppm) or feeding (15,000 and 20,000 ppm) were negative in this assay.

Dibutyltin diacetate was evaluated for mutagenicity in the Salmonella/microsome preincubation assay using a standard protocol approved by the National Toxicology Program. Dibutyltin diacetate was tested at doses of 0, 33, 100, 333, 1000, and 3333 ug/plate in four Salmonella typhimurium strains (TA98, TA100, TA1535, and TA1537) in the presence and absence of Aroclor-induced rat or hamster liver S9. Dibutyltin diacetate was negative in these tests and the highest ineffective dose level tested in any Salmonella tester strain was 3333 ug/plate.

... Under the conditions of this bioassay, there was no ... evidence of carcinogenicity for dibutyltin diacetate in male Fischer 344 rats or B6C3F1 mice of either sex. The loss of tissues taken from high dose female rats /reduced the sensitivity in this/ bioassay ... for female Fischer 344 rats. Levels of Evidence of Carcinogenicity: Male Rats: Negative; Female Rats: Inadequate Study; Male Mice: Negative; Female Mice: Negative.

Evidence for CarcinogenicityA4; Not classifiable as a human carcinogen. /Tin, organic compounds, as Sn/
National Toxicology Program Studies · 1 Eintrag

A bioassay for the possible carcinogenicity of dibutyltin diacetate was conducted using Fischer 344 rats and B6C3F1 mice. Dibutyltin diacetate was admin in the feed, at either of two concn, to groups of 50 male and 50 female animals of each species. Twenty animals of each sex and species were placed on test as controls. The high and low time weighted avg dietary concn of dibutyltin diacetate were, respectively, 133 and 66.5 ppm for rats and 152 and 76 ppm for mice. The cmpd was admin for 78 wk to rats and mice, followed by a period of no cmpd admin of 26 wk for rats and 14 wk for mice. ... Under the conditions of this bioassay, there was no ... evidence of carcinogenicity for dibutyltin diacetate in male Fischer 344 rats or B6C3F1 mice of either sex. The loss of tissues taken from high dose female rats /reduced the sensitivity in this/ bioassay ... for female Fischer 344 rats. Levels of Evidence of Carcinogenicity: Male Rats: Negative; Female Rats: Inadequate Study; Male Mice: Negative; Female Mice: Negative.

Toxicity DataLD50: 32 mg/kg (Oral, Rat) (T14) LD50: 18 mg/kg (Intravenous, Mouse) (T14)
Non-Human Toxicity Values · 4 Einträge

LD50 Rat oral 32 mg/kg

LD50 Mouse oral 46 mg/kg

LD50 Mouse intravenous 18 mg/kg

LD50 MOUSE ORAL 109.7 MG/KG

Regulatorische Informationen

Regulatory Information · 5 Einträge

Chemical: Stannane, bis(acetyloxy)dibutyl-

Hazard Traits - Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B;Report - if used as a fragrance or flavor ingredient

Acetic acid, 1,1'-(dibutylstannylene) ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, 1,1'-(dibutylstannylene) ester 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)

Status: Active Update: 30-06-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/13153

Dibutyltin diacetate: Does not have an individual approval but may be used under an appropriate group standard

State Drinking Water Guidelines(MN) MINNESOTA 4000 ug/l /Tin/
Impurities... IT IS EXTREMELY DIFFICULT TO PREPARE DIALKYLTIN COMPOUNDS AS PURE COMPOUNDS, THERE GENERALLY BEING PRESENT TRACES OF THE CORRESPONDING TRIALKYL DERIVATIVES. /DIALKYLTIN COMPOUNDS/
U.S. Production · 2 Einträge

2023: 50,000 - <75,000 lb;2022: 100,000 - <250,000 lb;2021: 75,000 - <100,000 lb;2020: 50,000 - <75,000 lb

(1975) PROBABLY GREATER THAN 4.54X10+5 G

Consumption Patterns · 1 Eintrag

The use of organotin compounds to stabilize polymers and copolymers of vinyl chloride results from research performed in the 1930s. However, it was not until 1946 that organotins were made generally available. For approximately the next 7 years, the family of compounds proliferated rapidly and were used in all type of vinyl processing situations. In the early 1950s, mixed-metal stabilizer combinations displaced organotins in almost all processing operations employing plasticized vinyl compounds. Mixed-metal stabilizer combinations have not been able to compete successfully with organotin mercaptides in applications involving unplasticized polyvinyl chloride.

Consumer UsesStabilizing agent
Industry UsesCatalyst;Processing aids not otherwise specified
Methods of ManufacturingReaction of acetic acid with dibutyltin oxide
Household ProductsInformation on 2 consumer products that contain Dibutyltin diacetate in the following categories is provided:;• Inside the Home
General Manufacturing Information · 4 Einträge

Miscellaneous Manufacturing;All Other Basic Organic Chemical Manufacturing;All Other Chemical Product and Preparation Manufacturing

Acetic acid, 1,1'-(dibutylstannylene) ester: ACTIVE

Organotin stabilizers are all derivatives of tetravalent tin. ... The organic groups bonded to tin are either alkyl or, substituted alkyl. Aryltin compounds have been shown to be poor stabilizers for polyvinyl chloride. /Organotin cmpd/

With regard to heat stabilizing efficacy, it is generally accepted that the dialkyltin compounds containing 2 anionic substituents are better than either the monoalkyl- or trialkyltin derivatives. /Dialkyltin compounds/