1,2-Ethanediamine, acetate (1:2) - ≥95% , CAS No.38734-69-9

CAS: 38734-69-9 Cat. No.: E300209 Peso molecular: 180.2

GRADE & PURITY ≥95%

Synonyms

DTXSID10436235 | Ethylenediamine diacetate | 1,2-Ethanediamine, diacetate | Ethane-1,2-diaminediacetate | SCHEMBL26819 | Ethylenediamine diacetate, 98% | MFCD00192147 | 1,2-Ethanediamine, acetate (1:2) | AKOS025295272 | Ethylenediamine diacetate 420352_AL

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

DTXSID10436235 | Ethylenediamine diacetate | 1, 2-Ethanediamine, diacetate | Ethane-1, 2-diaminediacetate | SCHEMBL26819 | Ethylenediamine diacetate, 98% | MFCD00192147 | 1, 2-Ethanediamine, acetate (1:2) | AKOS025295272 | Ethylenediamine diacetate 420352_AL

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 488196558
• Sonrisas canónicas: CC(=O)O.CC(=O)O.C(CN)N
• IUPAC Name: acetic acid;ethane-1,2-diamine
• InChIKey: SAXQBSJDTDGBHS-UHFFFAOYSA-N
• INCHI: 1S/C2H8N2.2C2H4O2/c3-1-2-4;2*1-2(3)4/h1-4H2;2*1H3,(H,3,4)
• Isómeros SMILES: CC(=O)O.CC(=O)O.C(CN)N
• Peso molecular: 180.2
• Reaxy-Rn: 5444394
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5444394&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• 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

• Punto de fusión (°C): 118-120 °C
• Peso molecular: 180.200 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 180.111 Da
• Monoisotopic Mass: 180.111 Da
• Topological Polar Surface Area: 127.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 37.000
• 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: 3

XLogP3

Referencias

1. Guanrui Huang, Haotian Shen, Kaiwang Xu, Yifan Shen, Jiale Jin, Guangyu Chu, Hongyuan Xing, Zhiyun Feng, Yue Wang.  (2024)  Single-Cell Microgel Encapsulation Improves the Therapeutic Efficacy of Mesenchymal Stem Cells in Treating Intervertebral Disc Degeneration via Inhibiting Pyroptosis.  Research,      [PMID:38371273] [10.34133/research.0311]

2. Xiangmei Wang, Huimin Zhang, Pengru Chen, Chuntao Chen, Dongping Sun, Xin Xiao, Bo Pang.  (2026)  Engineering g-C3N4 with chlorine for efficient visible-light photocatalysis: Mechanistic insights into charge separation and pollutant degradation.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:41519089] [10.1016/j.jenvman.2025.128526]