Formamidine Hydroiodide (Low water content) - ≥98%(T) , CAS No.879643-71-7

CAS: 879643-71-7 Cat. No.: F156688 Peso molecular: 171.97 Número EC: 827-106-7

GRADE & PURITY ≥98%(T)

Synonyms

methanimidamide hydroiodide | SCHEMBL7272878 | A901154 | ethanimidamide, hydriodide (1:1) | Formamidine Hydroiodide (Low water content) | Formimidamide hydroiodide | MFCD28369273 | Formamidine Hydroiodide (99.99%, trace metals basis) [for Perovskite precu

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

methanimidamide hydroiodide | SCHEMBL7272878 | A901154 | ethanimidamide, hydriodide (1:1) | Formamidine Hydroiodide (Low water content) | Formimidamide hydroiodide | MFCD28369273 | Formamidine Hydroiodide (99.99%, trace metals basis) [for Perovskite precu

Especificaciones y pureza

≥98%(T)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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

Pureza

≥98%(T)

Nombres e identificadores

• Sonrisas canónicas: C(=N)N.I
• IUPAC Name: methanimidamide;hydroiodide
• InChIKey: QHJPGANWSLEMTI-UHFFFAOYSA-N
• INCHI: 1S/CH4N2.HI/c2-1-3;/h1H,(H3,2,3);1H
• Isómeros SMILES: C(=N)N.I
• Peso molecular: 171.97
• Reaxy-Rn: 3667748
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3667748&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amidines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amidines
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxamidines
• Alternative Parents: Formamidines Carboximidamides Imines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Formamidine - Carboximidamide - Carboxylic acid amidine - Hydrocarbon derivative - Imine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxamidines. These are carboxylic acid derivatives containing the amidine group.
• 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: Soluble in water; Soluble in Dimethylformamide
• Sensibilidad: Air/Moisture/Light sensitive
• Punto de fusión (°C): 242 °C(dec.)
• Peso molecular: 171.969 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 171.95 Da
• Monoisotopic Mass: 171.95 Da
• Topological Polar Surface Area: 49.900 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.300
• 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. Qiangqiang Wang, Shuo Ding, Siliang He, Ting Zhang, Lei Qian, Peng Xiao, Tao Chen, Chaoyu Xiang.  (2022)  Improving the Operational Stability of Near-Infrared Quasi-2D Perovskite Light-Emitting Diodes by Cation Engineering.  Advanced Optical Materials,  11  (1): (2201778).  [PMID:] [10.1002/adom.202201778]

2. Yongqi Yin, Xisheng Zhang, Ho Ngoc Nam, Quan Manh Phung, Kuina Yuan, Boyuan Li, Fanyue Kong, Azhar Alowasheeira, Baoning Wang, Lin Li, Yusuke Yamauchi.  (2025)  Enhanced Efficiency and Stability of Tin Halide Perovskite Solar Cells Through MOF Integration.  Small,      [PMID:39865966] [10.1002/smll.202411346]

3. Peng Gao, Jianxin Xu, Zhanfei Zhang, Lijie Sun, Wenhua Li, Yonggang Guo, Kai Wang, Dayong Qiao, Binghe Ma, Weizheng Yuan, Tao Ye.  (2025)  Targeted PbI2 Removal Unlocks 31.71% Efficiency Perovskite-Silicon 2T Tandem Solar Cells.  Solar RRL,      [PMID:] [10.1002/solr.202500393]

4. Mingming Li, Ying Yue, Di Zhang, Yuejuan Zhang, Yanchun Wang, Xiao Zhang, Xiaojun Wei, Huaping Liu, Weiya Zhou.  (2025)  Lightweight and ultra-flexible perovskite solar cells with 'sandwich' perovskite layer based on graphene-carbon nanotube electrodes.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA06002H]

5. Xinxin Xu, Qiang Lou, Jiahao Wu, Haocheng Huang, Hao Zhang, Bosen Zhang, Maojun Sun, Lin Zhao, Jingyi Xu, Hang Zhou.  (2025)  Buried Interface Passivation of Regular Perovskite Solar Cells Using Trimethoxysilane-Based Small Molecule Materials.  ACS Applied Materials & Interfaces,      [PMID:40101194] [10.1021/acsami.5c01522]

6. Wenjuan Jiang, Cheng Peng, Haokun Jiang, Mingzhe Zhu, Zhongmin Zhou.  (2025)  Ion-migration-induced dual interface dipoles for high-performance perovskite solar cells.  Matter,      [PMID:] [10.1016/j.matt.2025.102085]

7. Hai Huang, Zijian Geng, Ankang Wan, Chunyan Cao, Daqin Chen, An Xie.  (2025)  Zn2+-Doped CsPbI3/PVDF Composite Films with Enhanced Stability and Photoluminescence Quantum Yield for White-Light LED Applications.  ACS Applied Materials & Interfaces,      [PMID:41269054] [10.1021/acsami.5c16923]

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9. Zihui Li, Jifei Ge, Chengbo Wang, Bin Tong, Gaoling Yang, Haizheng Zhong, Yuping Dong, Jianbing Shi.  (2026)  Direct In Situ Cascade Photolithography of Perovskite Quantum Dot Patterns with High Light Conversion Efficiency and Enhanced Stability.  ACS Applied Materials & Interfaces,      [PMID:41498533] [10.1021/acsami.5c23696]