1-Iodododecane (stabilized with Copper chip) - ≥98%(GC) , CAS No.4292-19-7

CAS: 4292-19-7 Cat. No.: I157556 Formula: C₁₂H₂₅I Peso molecolare: 296.24 Beilstein Registry Number: 1738940 Numero EC: 224-293-1

GRADE & PURITY ≥98%(GC)

Synonyms

A826068 | InChI=1/C12H25I/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-12H2,1H3 | STR02749 | NCGC00260380-01 | DTXCID3029158 | EINECS 224-293-1 | NSC 9285 | GCDPERPXPREHJF-UHFFFAOYSA- | 1-IODODODECANE | 1-iodo-dodecane | 1-Iodododecane, 98% | EN300-83276 | MFCD00001

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

1-Iodododecane has been used in the preparation of: dodecylated graphite； alkyl functionalized single walled carbon nanotubes (SWNTs)；SmI2-mediated coupling of 1-iodododecane and 2-octanone in the presence of LiBr, LiCl and hexamethylphosphoramide (HMPA) has been studied.

Specifications

Sinonimi

A826068 | InChI=1/C12H25I/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-12H2,1H3 | STR02749 | NCGC00260380-01 | DTXCID3029158 | EINECS 224-293-1 | NSC 9285 | GCDPERPXPREHJF-UHFFFAOYSA- | 1-IODODODECANE | 1-iodo-dodecane | 1-Iodododecane, 98% | EN300-83276 | MFCD00001

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 488182607
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182607
• Sorrisi canonici: CCCCCCCCCCCCI
• IUPAC Name: 1-iodododecane
• InChIKey: GCDPERPXPREHJF-UHFFFAOYSA-N
• INCHI: 1S/C12H25I/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-12H2,1H3
• Isomeri SMILES: CCCCCCCCCCCCI
• WGK Germania: 3
• Peso molecolare: 296.24
• Beilstein: 1738940
• Reaxy-Rn: 1738943
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1738943&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
• Descrizione: 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

Proprietà chimiche e fisiche

• Solubilità: Not miscible or difficult to mix in water.
• Sensibilità: light and air and moisture sensitive
• Indice di rifrazione: 1.483-1.485
• Punto di infiammabilità (°F): 230 °F
• Punto di infiammabilità (°C): 110 ℃
• Punto di ebollizione (°C): 159-160℃
• Punto di fusione (°C): -3℃
• Peso molecolare: 296.230 g/mol
• XLogP3: 7.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 10
• Exact Mass: 296.1 Da
• Monoisotopic Mass: 296.1 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 81.200
• 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

Riferimenti

1. Linrui Jiang, Wenpeng Li, Qingshan Miao, Jing Yang, Shaoyun Shan, Hongying Su.  (2023)  Stimuli-Sensitive Dextran Hydrogel Composited with Clickable Reaction-Based Aggregation-Induced Emission Micelles: A Carrier of Hydrophobic Drugs.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.3c01603]

2. Yang Li, Fu Shengxiang, Liu Li, Cai Zhongyuan, Xia Chunchao, Song Bin, Gong Qiyong, Lu Zhiyun, Ai Hua.  (2021)  Tetraphenylethylene-conjugated polycation covered iron oxide nanoparticles for magnetic resonance/optical dual-mode imaging.  Regenerative Biomaterials,  8  (3):   [PMID:34211733] [10.1093/rb/rbab023]

3. Ahmed O. Alnajjar, Hany M. Abd El-Lateef.  (2021)  A novel approach to investigate the synergistic inhibition effect of nickel phosphate nanoparticles with quaternary ammonium surfactant on the Q235-mild steel corrosion: Surface morphology, electrochemical-computational modeling outlines.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2021.116125]

4. Kexin Pan, Liyuan Chen, Guangjun Tian, Juyue Zhou, Suying Xu, Leyu Wang.  (2025)  Boosting responses of fluorescent imaging probes toward sulfur dioxide through engineering side chain length.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40318266] [10.1016/j.saa.2025.126252]