2-Iodopropane - ≥99%, contains Copper chip as stabilizer, used for 2-Iodopropane (Isopropyl iodide) was used to prepare butyric and isobutyric acid. 2-Iodopropane is used as an alkylating agent in the conversion of phenols, alcohols, oximes, carboxylic ac

CAS: 75-30-9 Cat. No.: I105794 Fórmula: C₃H₇I Peso molecular: 169.99 Beilstein Registry Number: 1098244 Número CE: 200-859-3

GRADE & PURITY ≥99%, contains Copper chip as stabilizer

Synonyms

Isopropyl iodide | 2-IODOPROPANE | 2-IODO-PROPANE | Isopropyljodid | EINECS 200-859-3 | Propane, 2-iodo- | i-Propyl iodide | isopropyliodide | 2-Jodpropan [Czech] | 1-methylethyl iodide | 67K05OPZ0E | MFCD00001071 | C3H7I | 2-Propyl iodide | sec-Propyl io

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

Visão geral

2-Iodopropane is an organ iodine compound. It is commonly used as a homolytic and heterolytic alkylating agent and in the preparation of the α-isopropoxymethylene blocking group. Additionally, it acts as an intermediator in the conversion of thiocarbonate to alkene.

Specifications

Sinónimos

Isopropyl iodide | 2-IODOPROPANE | 2-IODO-PROPANE | Isopropyljodid | EINECS 200-859-3 | Propane, 2-iodo- | i-Propyl iodide | isopropyliodide | 2-Jodpropan [Czech] | 1-methylethyl iodide | 67K05OPZ0E | MFCD00001071 | C3H7I | 2-Propyl iodide | sec-Propyl io

Especificações e pureza

≥99%, contains Copper chip as stabilizer

Aplicação

2-Iodopropane (Isopropyl iodide) was used to prepare butyric and isobutyric acid. 2-Iodopropane is used as an alkylating agent in the conversion of phenols, alcohols, oximes, carboxylic acids, and heteroatomic compounds (indoles, pyridines, purines, tetra

Condições de armazenamento de armazenamento

Protected from light,Room temperature,Argon charged

Enviado em

FedEx DG Service

Pureza

≥99%

Nomes e identificadores

• Pubchem Sid: 504751072
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751072
• Sorrisos canónicos: CC(C)I
• IUPAC Name: 2-iodopropane
• InChIKey: FMKOJHQHASLBPH-UHFFFAOYSA-N
• INCHI: 1S/C3H7I/c1-3(2)4/h3H,1-2H3
• SMILES isoméricas: CC(C)I
• WGK Alemanha: 3
• RTECS: TZ4200000
• Número UN: 2392
• Peso molecular: 169.99
• Beilstein: 1098244
• Reaxy-Rn: 1098244
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098244&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Classe Organoiodides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Classe: Organoiodides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organoiodides
• Alternative Parents: Hydrocarbon derivatives Alkyl iodides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organoiodide - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as organoiodides. These are compounds containing a chemical bond between a carbon atom and an iodine atom.
• 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

Propriedades químicas e físicas

• Solubilidade: Soluble in water(1.4g/L).
• Sensibilidade: Light & Air sensitive.
• Índice de refração: 1.4950 to 1.5010
• Ponto de inflamação (°F): 107.6 °F
• Ponto de inflamação (°C): 42℃
• Ponto de ebulição (°C): 89～90°C
• Ponto de fusão (°C): -90°C
• Peso molecular: 169.990 g/mol
• XLogP3: 2.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 169.959 Da
• Monoisotopic Mass: 169.959 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.800
• 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

Referências

1. Hui Gao, Wenqi Niu, Chaoqun Huang, Yan Hong, Chengyin Shen, Hongmei Wang, Yan Lu, Xiaojing Chen, Lei Xia, Haihe Jiang, Yannan Chu.  (2014)  Rate constants of electron attachment to alkyl iodides measured by photoionization electron attachment ion mobility spectrometry (PI-EA-IMS).  INTERNATIONAL JOURNAL OF MASS SPECTROMETRY,      [PMID:] [10.1016/j.ijms.2014.11.001]

2. Zhang Wen, Zheng Wei, Huang Ping, Yang Dengfeng, Shao Zhiqing, Zhang Wei, Zhang Hao, Xie Zhi, Xu Jin, Chen Xueyuan.  (2025)  Intense upconverted ultraviolet emission of Er3+ through confined energy transfer in Yb3+/Er3+ co-doped Rb3InCl6.  Nature Communications,  16  (1): (1-10).  [PMID:40695775] [10.1038/s41467-025-58901-4]