Triphenyltin chloride - ≥96% , CAS No.639-58-7

CAS: 639-58-7 Cat. No.: T113537 Peso molecular: 385.47 Beilstein Registry Number: 524762 Número EC: 211-358-4 PubChem CID: 12540

GRADE & PURITY ≥96%

Synonyms

TRIPHENYLTIN CHLORIDE|639-58-7|Fentin chloride|Chlorotriphenyltin|Chlorotriphenylstannane|Triphenylchlorotin|Stannane, chlorotriphenyl-|Triphenylchlorostannane|Brestanol|chloro(triphenyl)stannane|TPTC|Aquatin|Tinmate|Phenostat-C|General chemicals 8993|Aqu

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

TRIPHENYLTIN CHLORIDE | 639-58-7 | Fentin chloride | Chlorotriphenyltin | Chlorotriphenylstannane | Triphenylchlorotin | Stannane, chlorotriphenyl- | Triphenylchlorostannane | Brestanol | chloro(triphenyl)stannane | TPTC | Aquatin | Tinmate | Phenostat-C | General chemicals 8993 | Aqu

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥96%

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)Cl
• IUPAC Name: chloro(triphenyl)stannane
• InChIKey: NJVOZLGKTAPUTQ-UHFFFAOYSA-M
• INCHI: 1S/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1
• Isómeros SMILES: C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)Cl
• WGK Alemania: 3
• RTECS: WH6860000
• PubChem CID: 12540
• Número ONU: 3146
• Grupo de embalaje: I
• Peso molecular: 385.47
• Beilstein: 524762
• Reaxy-Rn: 524762

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Metal aryls Triorganotin halide salts Organotin compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Metal aryl - Monocyclic benzene moiety - Triorganotin halide salt - Organic metal salt - Hydrocarbon derivative - Organic tin salt - Organic salt - Organotin compound - Organometallic compound - Organic post-transition metal moeity - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: organotin compound - chlorine molecular entity

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Punto de ebullición (°C): 240°C
• Punto de fusión (°C): 105°C
• Peso molecular: 385.500 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 385.988 Da
• Monoisotopic Mass: 385.988 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 240.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

XLogP3

Referencias

1. Xiuxiu Chen, Donghui Zhu, Fan Zhang, Ouyang Li, Fan Yang, Zhijun Bao.  (2023)  Exposure to triphenyltin impairs gut integrity, disturbs gut microbiota, and alters fecal metabolites.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:38043414] [10.1016/j.ecoenv.2023.115753]

2. Si-Qi Zhang, Ping Li, Shu-Wen He, Shao-Ying Xing, Zhi-Han Cao, Xue-Li Zhao, Cuici Sun, Zhi-Hua Li.  (2023)  Combined effect of microplastic and triphenyltin: Insights from the gut-brain axis.  Environmental Science and Ecotechnology,      [PMID:37096249] [10.1016/j.ese.2023.100266]

3. Cao Zhihan, Li Ping, Ru Jinchuang, Cao Xuqian, Wang Xu, Liu Bin, Li Zhi-Hua.  (2022)  Physiological responses of marine Chlorella sp. exposed to environmental levels of triphenyltin.  ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH,  30  (10): (26387-26396).  [PMID:36367644] [10.1007/s11356-022-23992-9]

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. 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]

6. Wei Zhang, XiaoLi Cheng, Xianfa Zhang, Yingming Xu, Shan Gao, Hui Zhao, Lihua Huo.  (2017)  High selectivity to ppb-level HCHO sensor based on mesoporous tubular SnO2 at low temperature.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2017.03.099]

7. 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,  7  (6): (3117-3124).  [PMID:] [10.1039/C6RA25491H]

8. Jiamiao Wang, Jurong Lv, Zheyu Shen, Yan Liu, Xia Gao, Qiang Chen, Pei Liang.  (2025)  Development of rapid and data-driven detection methods for organotin compounds from microplastics: Integrating theoretical and experimental Raman and SERS database.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.112836]

9. 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]

10. 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]

11. Xiuxiu Chen, Donghui Zhu, Renshan Ge, Zhijun Bao.  (2024)  Fecal transplantation of young mouse donors effectively improves enterotoxicity in elderly recipients exposed to triphenyltin.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:38417315] [10.1016/j.ecoenv.2024.116140]

12. Tengzhou Li, Luoxin Li, Bin Liu, Shaoying Xing, Ling Liu, Ping Li, Zhi-Hua Li.  (2024)  TPT disrupts early embryonic development and glucose metabolism of marine medaka in different salinites.  COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY,      [PMID:39251012] [10.1016/j.cbpc.2024.110035]

13. Yangyang Li, Ji Li, Ting Li, Xiaoli Cheng, Yingming Xu, Shan Gao, Lihua Huo.  (2025)  In-situ sulfidation of raspberry-like SnS/SnO2 heterostructure for enhanced Cl2 gas sensing performance at near room temperature.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.164479]