Malonamamidine hydrochloride - ≥98% , CAS No.34570-17-7

CAS: 34570-17-7 Cat. No.: A136566 Molecular Weight: 137.57 EC Number: 252-095-5

GRADE & PURITY ≥98%

Synonyms

2-carbamimidoylacetamide hydrochloride | MPRLIYNSZYJODI-UHFFFAOYSA-N | PROPANAMIDE, 3-AMINO-3-IMINO-, HYDROCHLORIDE (1:1) | 3-amino-3-iminopropanamide hydrochloride | SCHEMBL1485493 | MFCD00013007 | Malonamamidine hydrochloride | SY109396 | 3-amino-3-imin

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

Malonamamidine hydrochloride is a useful biochemical for proteomics research. A useful biochemical for proteomics research.

Specifications

Synonyms

2-carbamimidoylacetamide hydrochloride | MPRLIYNSZYJODI-UHFFFAOYSA-N | PROPANAMIDE, 3-AMINO-3-IMINO-, HYDROCHLORIDE (1:1) | 3-amino-3-iminopropanamide hydrochloride | SCHEMBL1485493 | MFCD00013007 | Malonamamidine hydrochloride | SY109396 | 3-amino-3-imin

Specifications & Purity

≥98%

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488194276
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488194276
• Canonical Smiles: C(C(=N)N)C(=O)N.Cl
• IUPAC Name: 3-amino-3-iminopropanamide;hydrochloride
• InChIKey: MPRLIYNSZYJODI-UHFFFAOYSA-N
• INCHI: 1S/C3H7N3O.ClH/c4-2(5)1-3(6)7;/h1H2,(H3,4,5)(H2,6,7);1H
• Isomeric SMILES: C(C(=N)N)C(=O)N.Cl
• WGK Germany: 3
• Molecular Weight: 137.57
• Reaxy-Rn: 3911763
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3911763&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid amides
          • Level6 Primary carboxylic acid amides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid amides
• Direct Parent: Primary carboxylic acid amides
• Alternative Parents: Carboximidamides Carboxamidines Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Primary carboxylic acid amide - Carboximidamide - Carboxylic acid amidine - Amidine - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
• 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

Chemical and Physical Properties

• Flash Point(°C): 144.6 °C
• Boil Point(°C): 315.4°C at 760 mmHg
• Melt Point(°C): 174-176 °C
• Molecular Weight: 137.570 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 137.036 Da
• Monoisotopic Mass: 137.036 Da
• Topological Polar Surface Area: 93.000 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 98.400
• 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

References

1. Mingjing Jin, Chenpeng Xi, You Chen, Wenbin Yuan, Miao Zeng, Zhongliang Yan, Xueying Yang, Chuanyao Luo, Zhaojin Wang, Arui Huang, Xiaowei Xu, Chang Yan, Aung Ko Ko Kyaw, Jinhui Tong, Shi Chen, Wen-Hua Zhang, Zhengguo Xiao, Guang Yang, Tom Wu, Yang Bai.  (2025)  Bidentate Anchoring Enables Concurrent Grain Orientation and Lattice Strain Mitigation in Wide-Bandgap Perovskites for High-Performance All-Perovskite Tandem Solar Cells.  ADVANCED MATERIALS,      [PMID:41085129] [10.1002/adma.202513281]