Bis(tributyltin) oxide - analytical standard , CAS No.56-35-9

CAS: 56-35-9 Cat. No.: T107352 Fórmula: C₂₄H₅₄OSn₂ Peso molecular: 596.1 Beilstein Registry Number: 745057 Número EC: 200-268-0 PubChem CID: 16682746

GRADE & PURITY Analytical standard

Synonyms

Bis-(tri-n-butylcin)oxid | OTBE | OTBE [French] | Oxybis(tributyltin) | Oxybis[tributylstannane] | SCHEMBL9470441 | AMY25031 | APQHKWPGGHMYKJ-UHFFFAOYSA- | Bis(tri-n-butyltin)oxide, technical grade | Distannoxane, 1,1,1,3,3,3-hexabutyl- | Lastanox F | Sta

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Descripción general

Employed in the synthesis of α,β-unsaturated methyl ketones， isoxazoles, fungicides, and bactericides.

Specifications

Sinónimos

Bis-(tri-n-butylcin)oxid | OTBE | OTBE [French] | Oxybis(tributyltin) | Oxybis[tributylstannane] | SCHEMBL9470441 | AMY25031 | APQHKWPGGHMYKJ-UHFFFAOYSA- | Bis(tri-n-butyltin)oxide, technical grade | Distannoxane, 1,1,1,3,3,3-hexabutyl- | Lastanox F | Sta

Especificaciones y pureza

analytical standard

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice,FedEx DG Service

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Patrón analítico

Nombres e identificadores

• Sonrisas canónicas: CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC
• IUPAC Name: tributyl(tributylstannyloxy)stannane
• InChIKey: APQHKWPGGHMYKJ-UHFFFAOYSA-N
• INCHI: 1S/6C4H9.O.2Sn/c6*1-3-4-2;;;/h6*1,3-4H2,2H3
• Isómeros SMILES: CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC
• WGK Alemania: 3
• RTECS: JN8750000
• PubChem CID: 16682746
• Número ONU: 2788
• Grupo de embalaje: I
• Peso molecular: 596.1
• Beilstein: 745057

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organo-post-transition metal compounds
      • Subclass Organotin compounds
        • Level5 Triorganotin compounds
          • Level6 Trialkyltins

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organo-post-transition metal compounds
• Subclass: Organotin compounds
• Intermediate Tree Nodes: Triorganotin compounds
• Direct Parent: Trialkyltins
• Alternative Parents: Organic tin salts Organic oxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkyltin - Organic metal salt - Organic oxygen compound - Hydrocarbon derivative - Organic tin salt - Organic salt - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkyltins. These are triorganotin compounds where the tin atom is linked to exactly three alkyl groups.
• External Descriptors: inorganic 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: Air & Moisture Sensitive
• Índice de refracción: 1.486
• Punto de inflamación (°C): 190°C
• Punto de ebullición (°C): 180°C
• Peso molecular: 596.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 20
• Exact Mass: 596.221 Da
• Monoisotopic Mass: 598.222 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 246.000
• 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. 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]

2. Jinlei Zeng, Yue Yang, Yibo Tang, Xu Xu, Xu Chen, Ganlu Li, Kequan Chen, Hui Li, Pingkai Ouyang, Weimin Tan, Jianjun Ma, Yaozong Liu, Ruiyuan Liang.  (2022)  Synthesis, Monomer Removal, Modification, and Coating Performances of Biobased Pentamethylene Diisocyanate Isocyanurate Trimers.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.1c04673]

3. Wenjing Ji, Guojie Zhao, Guilin Hu, Li Fan, Hua Deng, Qiang Fu.  (2021)  The enhancement in dielectric properties for PVDF based composites due to the incorporation of 2D TiO2 nanobelt containing small amount of MWCNTs.  COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING,      [PMID:] [10.1016/j.compositesa.2021.106493]

4. Hu Jin, Zhang Xinya.  (2017)  Catalytic selectivity and process optimization of the trimerization of toluene diisocyanate.  JOURNAL OF MATERIALS SCIENCE,  52  (20): (12524-12539).  [PMID:] [10.1007/s10853-017-1372-3]

5. Yue Yang, Qixu Hu, Feng He, Peng Ma, Ganlu Li, Hui Li, Kequan Chen.  (2024)  Reducing High-Molecular-Weight Oligomers in Biobased Pentamethylene Diisocyanate Trimers.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c01333]

6. Zekun Li, Jitao Liu, Mengshuang Chi, Xue Miao, Hanxiao Yang, Weiqi Cui, Aifang Yu, Junyi Zhai.  (2024)  Ultra-high output triboelectric nanogenerator based on synergies of material modification and charge pumping.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.148726]

7. Ruida Cao, Long Yang, Wenbo Hu, Biao Dong, Hongwei Song, Lin Xu.  (2025)  Janus-Structured TENG for Complex Dual-Mode Communication Using Water Medium Across 200 m.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202508124]

8. Zhijian Zhang, Zhongshan Zhou, Wujiu Jiang, Yuxing Tan.  (2026)  Mitochondrial apoptosis and DNA intercalation synergistically driven by organotin acridine-9-carboxylate complexes potent anticancer efficacy.  JOURNAL OF INORGANIC BIOCHEMISTRY,      [PMID:42520359] [10.1016/j.jinorgbio.2026.113422]