Ethylenediaminetetraacetic Acid Tetrasodium Salt Dihydrate - for cell culture, ≥99% , CAS No.10378-23-1

CAS: 10378-23-1 Cat. No.: E118627 Peso molecular: 416.2 Beilstein Registry Number: 3861753 Número EC: 600-485-4

GRADE & PURITY for Cell culture, ≥99%

Synonyms

10378-23-1|Ethylenediaminetetraacetic acid tetrasodium salt dihydrate|Tetrasodium ethylenediaminetetraacetate dihydrate|3JGX4KKZ4A|tetrasodium edetate dihydrate|Acetic acid, (ethylenedinitrilo)tetra-, tetrasodium salt, dihydrate|67401-50-7|tetrasodium;2-[

Storage

Room temperature

Shipped In

Normal

Descripción general

Ethylenediaminetetraacetic acid (EDTA) is a chelator of metal ions. It is a substituted diamine, which has antibacterial activity. EDTA removes the undesirable effects of ferric, cupric and manganic ions in bleaching. It prevents cellular division, chlorophyll synthesis and algal biomass production. EDTA is an inhibitor of metalloprotease. It has anticoagulant property.

Specifications

Sinónimos

10378-23-1 | Ethylenediaminetetraacetic acid tetrasodium salt dihydrate | Tetrasodium ethylenediaminetetraacetate dihydrate | 3JGX4KKZ4A | tetrasodium edetate dihydrate | Acetic acid, (ethylenedinitrilo)tetra-, tetrasodium salt, dihydrate | 67401-50-7 | tetrasodium;2-[

Especificaciones y pureza

for cell culture, ≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

for Cell culture

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 504769088
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769088
• Sonrisas canónicas: C(CN(CC(=O)[O-])CC(=O)[O-])N(CC(=O)[O-])CC(=O)[O-].O.O.[Na+].[Na+].[Na+].[Na+]
• IUPAC Name: tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;dihydrate
• InChIKey: KSYNLCYTMRMCGG-UHFFFAOYSA-J
• INCHI: 1S/C10H16N2O8.4Na.2H2O/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20;;;;;;/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20);;;;;2*1H2/q;4*+1;;/p-4
• Isómeros SMILES: C(CN(CC(=O)[O-])CC(=O)[O-])N(CC(=O)[O-])CC(=O)[O-].O.O.[Na+].[Na+].[Na+].[Na+]
• WGK Alemania: 2
• CAS alternativo: 64-02-8
• Peso molecular: 416.2
• Beilstein: 3861753
• Reaxy-Rn: 14193382
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14193382&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Tetracarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetracarboxylic acids and derivatives
• Alternative Parents: Alpha amino acids Trialkylamines Carboxylic acid salts Amino acids Carboxylic acids Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetracarboxylic acid or derivatives - Alpha-amino acid - Alpha-amino acid or derivatives - Amino acid or derivatives - Amino acid - Carboxylic acid salt - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid - Organic alkali metal salt - Organic sodium salt - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Organic oxygen compound - Organic salt - Organic zwitterion - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.
• 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): 300°C
• Peso molecular: 416.200 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 7
• Exact Mass: 416.04 Da
• Monoisotopic Mass: 416.04 Da
• Topological Polar Surface Area: 169.000 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 293.000
• 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: 7

XLogP3

Referencias

1. Baolong Mi, Da Sheng, Bin Liu, Lingjun Bu, Zhou Shi, Shiqing Zhou, Shumin Zhu.  (2023)  Polyamide nanofiltration membrane fabricated via a metal-chelate strategy for high-flux desalination.  DESALINATION,      [PMID:] [10.1016/j.desal.2023.117049]

2. Xue Jiang, Yanxing Wang, Danyang Xu, Bi Lin, Fan Yang, Ruichan Lv.  (2020)  Lanthanide-Based Nanocomposites for Photothermal Therapy under Near-Infrared Laser: Relationship between Light and Heat, Biostability, and Reaction Temperature.  LANGMUIR,      [PMID:32188251] [10.1021/acs.langmuir.0c00343]

3. Chang Liu, Long Yan, Lulu Zhu, Yang Yu, Yuehui Tai, Yunjiang Yu, Qifeng Liu, Liangzhong Li.  (2024)  Highly efficient removal of tetrabromobisphenol A by Fenton degradation with iron-modulated zeolite under nanoconfinement.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2024.134537]

4. Siqinbilige Wu, Jingxian Gao, Yinzhabu Bai, Zhen Bai, Changxi Bai.  (2024)  Urinary metabolomic analysis of three fundamental traditional Mongolian Medicine Constitution types using UHPLC-QTOF-MS and nuclear magnetic resonance techniques.  Journal of Radiation Research and Applied Sciences,      [PMID:] [10.1016/j.jrras.2024.100915]

5. Ruohan Liang, Dongsheng Zhao, Fangming Jin, Jun Xu, Guicai Liu.  (2026)  Engineering a nanofiltration membrane with high mono-/divalent anion selectivity and antifouling properties via L-histidine incorporation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2026.136851]