Tributyltin chloride - ≥96% , CAS No.1461-22-9

CAS: 1461-22-9 Cat. No.: T104678 Peso molecular: 325.51 Beilstein Registry Number: 3535715 Número EC: 215-958-7 PubChem CID: 15096
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
CCRIS 6319 | Tri(n-butyl) tin chloride | TRIBUTYL TIN CHLORIDE | Tri-butyl tin chloride | Tributylchlorotin | Tri-n-butylchlorotin | C12H27ClSn | DTXSID3027403 | tri-n-butyltinchloride | F0001-0521 | MFCD00000521 | tributylstannanylium;chloride | TBTC, PE
Storage
Room temperature,Argon charged,Desiccated,Cool
Shipped In
FedEx DG Service
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Size
Estado
Price
Qty
25g
T104678-25g
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19,90US$
100g
T104678-100g
2

48,90US$

49,90US$
Guardar 1,00 US$ (2.00%)
500g
T104678-500g
2

131,90US$

149,90US$
Guardar 18,00 US$ (12.01%)
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged,Desiccated,Cool Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 26 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
CCRIS 6319 | Tri(n-butyl) tin chloride | TRIBUTYL TIN CHLORIDE | Tri-butyl tin chloride | Tributylchlorotin | Tri-n-butylchlorotin | C12H27ClSn | DTXSID3027403 | tri-n-butyltinchloride | F0001-0521 | MFCD00000521 | tributylstannanylium;chloride | TBTC, PE
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged, Desiccated, Cool
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥96%
Nombres e identificadores
Pubchem Sid504752633
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504752633
Sonrisas canónicasCCCC[Sn](CCCC)(CCCC)Cl
IUPAC Nametributyl(chloro)stannane
InChIKeyGCTFWCDSFPMHHS-UHFFFAOYSA-M
INCHI1S/3C4H9.ClH.Sn/c3*1-3-4-2;;/h3*1,3-4H2,2H3;1H;/q;;;;+1/p-1
Isómeros SMILES CCCC[Sn](CCCC)(CCCC)Cl
WGK Alemania 3
RTECS WH6820000
PubChem CID 15096
Número ONU 2788
Peso molecular 325.51
Beilstein 3535715

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic salts
ClaseOrganic metal salts
SubclassOrganic post-transition metal salts
Intermediate Tree Nodes Organic tin salts
Direct ParentTriorganotin halide salts
Alternative Parents Trialkyltins  Metal alkyl halides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Triorganotin halide salt - Trialkyltin - Metal alkyl halide - Hydrocarbon derivative - Organotin compound - Organometallic compound - Organic post-transition metal moeity - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as triorganotin halide salts. These are organic compounds containing a tin atom bonded to three carbon atoms and a halogen atom.
External Descriptors inorganic molecular entity
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

22 results found

Lot NumberCertificate TypeFechaArticulo
F2315953Certificate of AnalysisMar 18, 2026 T104678
F2315949Certificate of AnalysisMar 18, 2026 T104678
F2315943Certificate of AnalysisMar 18, 2026 T104678
B2627612Certificate of AnalysisFeb 03, 2026 T104678
B2627650Certificate of AnalysisFeb 03, 2026 T104678
B2627651Certificate of AnalysisFeb 03, 2026 T104678
B2627652Certificate of AnalysisFeb 03, 2026 T104678
H2529684Certificate of AnalysisJun 19, 2025 T104678
H2529683Certificate of AnalysisJun 19, 2025 T104678
H2529682Certificate of AnalysisJun 19, 2025 T104678
H2529681Certificate of AnalysisJun 19, 2025 T104678
F2223409Certificate of AnalysisApr 02, 2025 T104678
C2525809Certificate of AnalysisJul 13, 2024 T104678
C2525803Certificate of AnalysisJul 13, 2024 T104678
C2127137Certificate of AnalysisJan 10, 2024 T104678
C2526041Certificate of AnalysisMay 31, 2023 T104678
F2315948Certificate of AnalysisMay 31, 2023 T104678
B2515039Certificate of AnalysisMay 31, 2023 T104678
C2127139Certificate of AnalysisMay 17, 2023 T104678
C2024027Certificate of AnalysisJan 26, 2023 T104678
F2223399Certificate of AnalysisJun 05, 2022 T104678
F2223400Certificate of AnalysisJun 05, 2022 T104678

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Propiedades químicas y físicas
SolubilidadMiscible with alcohol, heptane, benzene and toluene. Immiscible with water.
SensibilidadMoisture sensitive;Hygroscopic
Índice de refracción1.4903
Punto de inflamación (°F)>112℃
Punto de inflamación (°C)>112℃
Punto de ebullición (°C)145-147°C
Punto de fusión (°C)-9°C
Peso molecular325.500 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count9
Exact Mass326.082 Da
Monoisotopic Mass326.082 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity104.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Shaowen Pei, Xiuping Ju, Jinsheng Zhao, Hongmei Du.  (2023)  Synthesis and Electrochromic Properties of Two Random Copolymers Containing Benzotriazole, Benzothiadiazole as Electron Acceptors and Benzodithiophene or Indacenodithiophene as Electron Donors.  International Journal of Electrochemical Science,      [PMID:] [10.20964/2019.07.23]
2. Lanlan Shen, Zhiru Bai, Yu Jiang, Liying Li, Fengxing Jiang, Jingkun Xu, Huanhuan Qiu, Huixuan Liu, Rongri Tan.  (2023)  Electrosynthesis and Spectroelectrochemistry Properties of Copolymers Based on 3,4-Ethylenedioxythiophene and Quaterthiophenen Derivatives.  International Journal of Electrochemical Science,      [PMID:] [10.20964/2020.09.73]
3. Shuang Chen, Lingqian Kong, Chaolei Ban, Jinsheng Zhao, Hongmei Du.  (2023)  Synthesis and Characterization of Four Random copolymers Containing Fluorene as Electron Donors and Benzotriazole, Benzothiadiazole, Pyrido[3,4-b]pyrazine as Electron Acceptors.  International Journal of Electrochemical Science,      [PMID:] [10.20964/2018.10.16]
4. Qiaoqiao Wang, Jingjing Miao, Anran Zhao, Manni Wu, Luqing Pan.  (2022)  Use of GAL4 factor-based yeast assay to quantify the effects of xenobiotics on RXR homodimer and RXR/PPAR heterodimer in scallop Chlamys farreri.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:36063929] [10.1016/j.scitotenv.2022.158526]
5. Xiaochong Song, Qing Luo, Xiaojia Huang.  (2022)  Speciation of organotin compounds in water and seafood samples by online hyphenation of porous polymer-based magnetism-enhanced in-tube solid phase microextraction and HPLC.  ANALYTICA CHIMICA ACTA,      [PMID:35998999] [10.1016/j.aca.2022.340175]
6. Rui Li, Haoran Xu, Yuhang Zhang, Lijing Chang, Yang Ma, Yanjun Hou, Shoulei Miao, Cheng Wang.  (2021)  Electrochromic properties of pyrene conductive polymers modified by chemical polymerization.  RSC Advances,  11  (62): (39291-39305).  [PMID:35492490] [10.1039/D1RA07977H]
7. Yuhang Zhang, Rui Li, Lijing Chang, Yang Ma, Yanjun Hou, Haijun Niu.  (2021)  Electropolymerization of Thiophene-Based Monomers with Different Spatial Structures: The Impact of Monomer Structure on Electrochromic Properties.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  223  (2): (2100341).  [PMID:] [10.1002/macp.202100341]
8. Lijing Chang, Yanjun Hou, Ju Bai, Haoran Xu, Yuhang Zhang, Shoulei Miao, Cheng Wang.  (2021)  Optoelectronic/memory storage properties of triphenylamine-based dual-function electrochromic materials.  MATERIALS CHEMISTRY AND PHYSICS,      [PMID:] [10.1016/j.matchemphys.2021.125196]
9. Haoran Xu, Yanjun Hou, Rui Li, Lijing Chang, Yang Ma, Shoulei Miao, Haijun Niu.  (2021)  D-A type hybrid polymers based on EDOT and various benzodiazoles for electrochromic materials.  JOURNAL OF APPLIED POLYMER SCIENCE,  138  (36): (50926).  [PMID:] [10.1002/app.50926]
10. Jing Zhan, Xiaoran Ma, Donghui Liu, Yiran Liang, Peize Li, Jingna Cui, Zhiqiang Zhou, Peng Wang.  (2020)  Gut microbiome alterations induced by tributyltin exposure are associated with increased body weight, impaired glucose and insulin homeostasis and endocrine disruption in mice.  ENVIRONMENTAL POLLUTION,      [PMID:32835916] [10.1016/j.envpol.2020.115276]
11. Huiyu He, Miaomiao Tian, Lihuan Hu, Li Yang.  (2020)  Ultrasensitive determination of organotin compounds in plastic food packaging and edible oils by sheathless capillary electrophoresis-electrospray ionization-mass spectrometry.  ANALYST,  145  (6): (2286-2296).  [PMID:32003368] [10.1039/C9AN02331C]
12. Zhen Xu, Yuling Zhang, Bozhen Wang, Zhi Liu, Jinsheng Zhao, Yu Xie.  (2019)  Yellow-to-blue switching of indole[3,2-b]carbazole-based electrochromic polymers and the corresponding electrochromic devices with outstanding photopic contrast, fast switching speed, and satisfactory cycling stability.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2019.02.054]
13. Yan Zhang, Lingqian Kong, Hongmei Du, Jinsheng Zhao, Yu Xie.  (2018)  Three novel donor-acceptor type electrochromic polymers containing 2,3-bis(5-methylfuran-2-yl)thieno[3,4-b]pyrazine acceptor and different thiophene donors: Low-band-gap, neutral green-colored, fast-switching materials.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2018.10.020]
14. Jianzhong Xu, Qi Ji, Lingqian Kong, Hongmei Du, Xiuping Ju, Jinsheng Zhao.  (2018)  Soluble Electrochromic Polymers Incorporating Benzoselenadiazole and Electron Donor Units (Carbazole or Fluorene): Synthesis and Electronic-Optical Properties.  Polymers,  10  (4): (450).  [PMID:30966485] [10.3390/polym10040450]
15. Shuai Li, Guoliang Liu, Xiuping Ju, Yan Zhang, Jinsheng Zhao.  (2017)  Synthesis, Characterization and Application of Four Novel Electrochromic Materials Employing Nitrotriphenylamine Unit as the Acceptor and Different Thiophene Derivatives as the Donor.  Polymers,  (5): (173).  [PMID:30970853] [10.3390/polym9050173]
16. Zhen Liu, Le Wang, Weiwei Bian, Min Zhang, Jinhua Zhan.  (2017)  Porous silver coating fiber for rapidly screening organotin compounds by solid phase microextraction coupled with surface enhanced Raman spectroscopy.  RSC Advances,  (6): (3117-3124).  [PMID:] [10.1039/C6RA25491H]
17. Yan Zhang, Lingqian Kong, Xuezhong Liu, Chunlei Wang, Jinsheng Zhao.  (2016)  Two New Bithiophenes Derivatives Multielectrochromic Copolymer Based on Triphenylamine Unit and Their Application for Electrochromic Devices.  BULLETIN OF THE KOREAN CHEMICAL SOCIETY,  37  (8): (1234-1243).  [PMID:] [10.1002/bkcs.10844]
18. Shuang Chen, Di Zhang, Min Wang, Lingqian Kong, Jinsheng Zhao.  (2015)  Donor–acceptor type polymers containing the 2,3-bis(2-pyridyl)-5,8-dibromoquinoxaline acceptor and different thiophene donors: electrochemical, spectroelectrochemistry and electrochromic properties.  NEW JOURNAL OF CHEMISTRY,  40  (3): (2178-2188).  [PMID:] [10.1039/C5NJ02651B]
19. Huang Yuanyuan, Yang Qingwei, Song Ling, Ran Hongjie, Jiang Hui, Sun Da.  (2024)  Efficient eradication of organotin utilizing K2FeO4 augmented by nZVI: revelations on influential factors, kinetic dynamics, and mechanistic insights.  Frontiers in Environmental Science,      [PMID:] [10.3389/fenvs.2024.1358297]
20. Songlin Wang, Chi Chen, Peng Yang, Yu Guo, Bingxing Wang, Hongying Niu, Qiying Zhang, Jianji Wang.  (2024)  Facile One-Pot Preparation of Organotin-Oxometalate Polymers for Efficient Synthesis of Dimethyl Carbonate from CO2.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c00937]
21. Yiren Xiong, Guoqiang Guo, Hongyi Xian, Zuqing Hu, Di Ouyang, Jiayi He, Shanshan He, Renyi Liu, Zhenjie Gao, Meilin Tang, Ying Chen, Suqin Tan, Xiaoqi Zhu, Abudumijiti Abulimiti, Sujin Zheng, Hehai Huang, Dalin Hu.  (2024)  MCF-7 cell - derived exosomes were involved in protecting source cells from the damage caused by tributyltin chloride via transport function.  TOXICOLOGY,      [PMID:38801937] [10.1016/j.tox.2024.153844]
22. Jiao Wang, Zhiyuan Mi, Caihong Lu, Zhenhua Han, Yuxin Wu, Xiaolong Fu, Guofang Zhang.  (2024)  Preparation of carbon nanotube-filled bismuth/tin green nanocomposites and their efficient catalytic activity in the thermal decomposition of ammonium perchlorate.  Surfaces and Interfaces,      [PMID:] [10.1016/j.surfin.2024.103866]
23. Binhua Mei, Ju Bai, Yuhang Zhang, Yang Ma, Yanjun Hou, Shuhong Wang, Cheng Wang.  (2024)  Synthesis of thienopyrazine- and cyclofluorene–thiophene-based donor–acceptor low-band gap polymers and their application in memory devices.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.55998]
24. Zipeng He, Binhua Mei, Hongmei Chu, Yanjun Hou, Haijun Niu.  (2023)  D–A Structural Oligomers Containing Benzothiadiazole or Benzophenone as Novel Multifunctional Materials for Electrochromic and Photodetector Devices.  Polymers,  15  (10): (2274).  [PMID:37242849] [10.3390/polym15102274]
25. Qi Zheng, Nan Hong, Lin Liu, Cong Wang, Ruixi Gan, Di Xu, Junsong Wang.  (2026)  Neurotoxic Effects of Acute Tributyltin Exposure in Adult Zebrafish: Behavioral Impairments and Mechanistic Insights.  Metabolites,  16  (2): (105).  [PMID:41745588] [10.3390/metabo16020105]
26. Gao Yuxuan, Kong Qiyu, Wang Jun, Sun Fengwei, Liu Xinyu, Wang Deliang, Li Jiangao, Yang Zhen.  (2026)  Well-tailored Photosensitizers with Boosted Type-I ROS Generation by Fluorination Strategy for Precise Near-infrared Fluorescence-guided Photodynamic Therapy.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,      [PMID:] [10.1007/s40242-026-5314-y]
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