Formamidine hydrochloride(FACl) - ≥96% , CAS No.6313-33-3

CAS: 6313-33-3 Cat. No.: F111100 Peso molecular: 80.52 Beilstein Registry Number: 3906935 Número EC: 228-639-2

GRADE & PURITY ≥96%

Synonyms

FORMAMIDINE, HYDROCHLORIDE | FT-0626527 | SB75370 | AKOS000260178 | Formimidamide hydrochloride | 2-hydroxy-4-methyl-3-nitro pyridine | FORMAMIDINE, MONOHYDROCHLORIDE | F0103 | formamidine HCl salt | NMVVJCLUYUWBSZ-UHFFFAOYSA-N | MFCD00012865 | A15719 | A

Storage

Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Descripción general

5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).

Specifications

Sinónimos

FORMAMIDINE, HYDROCHLORIDE | FT-0626527 | SB75370 | AKOS000260178 | Formimidamide hydrochloride | 2-hydroxy-4-methyl-3-nitro pyridine | FORMAMIDINE, MONOHYDROCHLORIDE | F0103 | formamidine HCl salt | NMVVJCLUYUWBSZ-UHFFFAOYSA-N | MFCD00012865 | A15719 | A

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged, Desiccated, Cool

Enviado en

Normal

Pureza

≥96%

Nombres e identificadores

• Sonrisas canónicas: C(=N)N.Cl
• IUPAC Name: methanimidamide;hydrochloride
• InChIKey: NMVVJCLUYUWBSZ-UHFFFAOYSA-N
• INCHI: 1S/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H
• Isómeros SMILES: C(=N)N.Cl
• WGK Alemania: 3
• Peso molecular: 80.52
• Beilstein: 3906935
• Reaxy-Rn: 3666426
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3666426&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 Organopnictogen compounds Imines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Formamidine - Carboximidamide - Carboxylic acid amidine - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - 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 Ethanol.
• Sensibilidad: Hygroscopic
• Punto de fusión (°C): 84-87°C
• Peso molecular: 80.520 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 80.0141 Da
• Monoisotopic Mass: 80.0141 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. Fangwen Cheng, Shaoqi Zhan, Xinfeng Dai, Xiaofeng Huang, Binghui Wu, Nanfeng Zheng.  (2021)  Low-Temperature Fabrication of Phase-Pure α-FAPbI3 Films by Cation Exchange from Two-Dimensional Perovskites for Solar Cell Applications.  ENERGY & FUELS,      [PMID:] [10.1021/acs.energyfuels.1c02175]

2. Hongwei Zhu, Lianghe Sun, Ming Lu, Yuangang Xu.  (2025)  Synthesis and characterization of a series of cyclo-N5− salts with layered stacking patterns.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2025.143111]