Tin(II) acetate - ≥95% , CAS No.638-39-1

CAS: 638-39-1 Cat. No.: T304247 Peso molecular: 236.8 Número EC: 211-335-9 PubChem CID: 69488

GRADE & PURITY ≥95%

Synonyms

UNII-1SKU167W8P | tin (II) acetate | STANNOUS ACETATE [MI] | SCHEMBL64390 | Diacetoxytin | DTXSID30213242 | 1SKU167W8P | Tin di(acetate) | EINECS 211-335-9 | tin(2+);diacetate | SCHEMBL64389 | tin(ii)acetate | Stannous acetate

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

• Used to prepare tin(IV) oxide thin films by photochemical vapor deposition. With palladium(II) acetate, an efficient catalytic system for C-H activation of the methoxy group of anisole.
• Enhances the rate of thermal depolymerization of poly(lactic acid) fibers
• Reactant for the synthesis of Sn-Cu bimetallic nanoparticles
• used in in preparation of tin anode by organic electroplating for rechargeable thin-film batteries
• Used as tin source for preparation of high surface area tin oxide catalysts

Specifications

Sinónimos

UNII-1SKU167W8P | tin (II) acetate | STANNOUS ACETATE [MI] | SCHEMBL64390 | Diacetoxytin | DTXSID30213242 | 1SKU167W8P | Tin di(acetate) | EINECS 211-335-9 | tin(2+);diacetate | SCHEMBL64389 | tin(ii)acetate | Stannous acetate

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 488184335
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184335
• Sonrisas canónicas: CC(=O)[O-].CC(=O)[O-].[Sn+2]
• IUPAC Name: tin(2+);diacetate
• InChIKey: PNOXNTGLSKTMQO-UHFFFAOYSA-L
• INCHI: 1S/2C2H4O2.Sn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
• Isómeros SMILES: CC(=O)[O-].CC(=O)[O-].[Sn+2]
• PubChem CID: 69488
• Peso molecular: 236.8

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid salts
          • Level6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Monocarboxylic acids and derivatives Carboxylic acids Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Acetate salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• External Descriptors: Not available

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

• Solubilidad: Decomposes in water. Soluble in dilute HClSoluble in dilute hydrochloric acid, dimethyl sulfoxide and methanol.
• Sensibilidad: Moisture sensitive
• Punto de fusión (°C): 180-182 °C (lit.)
• Peso molecular: 236.800 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 237.929 Da
• Monoisotopic Mass: 237.929 Da
• Topological Polar Surface Area: 80.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 25.500
• 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: 3

XLogP3

Referencias

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2. Qiuxia Zou, Hongshen He, Jie Xie, Shibo Han, Weijie Lin, Ajoy Kanti Mondal, Fang Huang.  (2023)  Study on the mechanism of acid modified H-Beta zeolite acidic sites on the catalytic pyrolysis of Kraft lignin.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142029]

3. Jianhua Xiao, Jiaao Wu, Fangchen Zhu, Jiehao Ke, Qingxia Liu, Yang Wang, Liu Yuan, Huiling Tai, Yadong Jiang.  (2024)  Bias-Switchable Dual-Mode Organic Photodiodes Enabled by Manipulation of Interface Layers.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202404711]

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5. Fengluan Jiang, Wenhe Xie, Yu Deng, Keyu Chen, Jichun Li, Xin-Yu Huang, Hongxiu Yu, Yaobang Li, Limin Wu, Yonghui Deng.  (2024)  Maillard Reaction Inspired Microexplosion toward Fast Synthesis of Two-Dimensional Mesoporous Tin Oxides for Efficient Chemiresistive Gas Sensing.  ACS Applied Materials & Interfaces,      [PMID:38795031] [10.1021/acsami.4c06072]

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8. Shengjun Zhang, Zhaochun Xu, Jingzhou Liu, Yue Cheng, Xiaojun Zeng.  (2025)  Strong electronic interactions stem from lattice strain control in PdSnCu nanochains for robust electrocatalytic ethanol oxidation.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2025.113920]

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