Tetramethylammonium iodide - ≥98% , CAS No.75-58-1

CAS: 75-58-1 Cat. No.: T100317 Peso molecular: 201.05 Beilstein Registry Number: 3620030 Número EC: 200-881-3 PubChem CID: 6381

GRADE & PURITY ≥98%

Synonyms

HY-W014861 | Q26840810 | AKOS015833289 | T0139 | Yodurtan | EINECS 200-881-3 | Banikol | SCHEMBL108581 | F87494 | TMAI | Tetramethyl ammonium iodide | UNII-L493Z502W3 | TRETRAMETHYLAMMONIUM IODIDE | ghl.PD_Mitscher_leg0.944 | RXMRGBVLCSYIBO-UHFFFAOYSA-M |

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Sinónimos

HY-W014861 | Q26840810 | AKOS015833289 | T0139 | Yodurtan | EINECS 200-881-3 | Banikol | SCHEMBL108581 | F87494 | TMAI | Tetramethyl ammonium iodide | UNII-L493Z502W3 | TRETRAMETHYLAMMONIUM IODIDE | ghl.PD_Mitscher_leg0.944 | RXMRGBVLCSYIBO-UHFFFAOYSA-M |

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: C[N+](C)(C)C.[I-]
• IUPAC Name: tetramethylazanium;iodide
• InChIKey: RXMRGBVLCSYIBO-UHFFFAOYSA-M
• INCHI: 1S/C4H12N.HI/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
• Isómeros SMILES: C[N+](C)(C)C.[I-]
• WGK Alemania: 3
• RTECS: PA1050000
• PubChem CID: 6381
• Número ONU: 2811
• Peso molecular: 201.05
• Beilstein: 3620030
• Reaxy-Rn: 3620030

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organopnictogen compounds Organic iodide salts Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic iodide salt - Organic salt - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
• 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

Objetivos asociados (humanos)

CHRNA1 Tclin Acetylcholine receptor protein alpha chain (98 Activities)

Discover Target: CHRNA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in water. Insoluble in chloroform, ether
• Sensibilidad: Moisture & Light sensitive
• Punto de fusión (°C): >300°C
• Peso molecular: 201.050 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 201.001 Da
• Monoisotopic Mass: 201.001 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 19.100
• 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: 2

XLogP3

Referencias

1. Qi Li, Yi-lei Li, Bo Li, Ying-juan Hao, Xiao-jing Wang, Rui-hong Liu, Yuan Ling, Xinying Liu, Fa-tang Li.  (2021)  Construction of adjustable dominant {314} facet of Bi5O7I and facet-oxygen vacancy coupling dependent adsorption and photocatalytic activity.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2021.120041]

2. Xuejiang Cheng, Xin Wang, Guangming Chen.  (2018)  A convenient and highly tunable way to n-type carbon nanotube thermoelectric composite film using common alkylammonium cationic surfactant.  Journal of Materials Chemistry A,  6  (39): (19030-19037).  [PMID:] [10.1039/C8TA07746K]

3. Yingli Wang, Jialong Duan, Yuanyuan Zhao, Benlin He, Zhengbo Jiao, Qunwei Tang.  (2018)  Hybridized dye-sensitized solar cells for persistent power generation free of sun illumination.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2018.05.090]

4. Wen-Wang Yu, Xiang-Guang Meng, Wen Li, Li-Yu Chen, Zi-Yu Gan, Yu-Lian Zhang, Jie Zhou.  (2024)  Highly efficient capture and conversion of CO2 into cyclic carbonates from actual flue gas under atmospheric pressure.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2024.113614]

5. Rui Zhu, Jun Wang, Hui Li, Ruyi Luo, Junsheng Tan, Ning Guo, Jianpeng Ma, Wen Wen, Yuchen Wu, Lei Jiang, Jiangang Feng.  (2026)  Overcoming Exciton Quenching at the ZnMgO/InP Quantum Dot Interface for Stable LEDs.  Small,      [PMID:41524609] [10.1002/smll.202513631]