Citric acid - UltraBio™, anhydrous, ≥99.5%(T) , CAS No.77-92-9

CAS: 77-92-9 Cat. No.: C755557 Fórmula: C₆H₈O₇ Peso molecular: 192.12 Beilstein Registry Number: 782061 Número CE: 201-069-1

GRADE & PURITY Anhydrous Grade, UltraBio™, ≥99.5%(T)

Storage

Room temperature,Argon charged

Shipped In

Normal

Visão geral

Citric acid is a buffer component for triple-column amino acid analysis. It is an optimal buffer for dissociation of radioiodinated antibodies from viable murine tumor cells.

Application:

• Enhancing soil microbiomes: Citric acid has been applied to modify soil bacterial communities in saline mudflats, demonstrating its utility in environmental biotechnology for sustainable ecosystem management (Liu et al., 2024).


• Biodegradable packaging in food industry: In food chemistry, citric acid is used in conjunction with polyvinyl alcohol for developing antimicrobial packaging, highlighting its potential in food safety and preservation (Xu et al., 2024).


• Nanomaterial synthesis for engineering applications: Citric acid serves as a key component in the eco-friendly synthesis of hybrid nanomaterials for supercapacitors, underpinning its role in advancing materials science and engineering (Teixeira et al., 2024).


• Environmental science and pollution control: Research utilizes citric acid to study the co-transport of pharmaceuticals and nanoparticles in environmental systems, aiding in the understanding of contaminant dynamics and mitigation strategies (Cui et al., 2024).


• Food science and technology: Citric acid is employed in the formulation of vegan gummies, indicating its versatility in food product development and its impact on textural properties (Rawat et al., 2024).

Specifications

Especificações e pureza

UltraBio™, anhydrous, ≥99.5%(T)

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Grau

Anhydrous Grade, UltraBio™

Pureza

≥99.5%(T)

Nomes e identificadores

PH

1.0-2.0 (25 °C, 1 M in H 2 O)

Sorrisos canónicos

C(C(=O)O)C(CC(=O)O)(C(=O)O)O

IUPAC Name

2-hydroxypropane-1,2,3-tricarboxylic acid

InChIKey

KRKNYBCHXYNGOX-UHFFFAOYSA-N

INCHI

1S/C6H8O7/c7-3(8)1-6(13,5(11)12)2-4(9)10/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

SMILES isoméricas

C(C(=O)O)C(CC(=O)O)(C(=O)O)O

WGK Alemanha

1

RTECS

GE7350000

Peso molecular

192.12

Beilstein

782061

Reaxy-Rn

782061

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=782061&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Tricarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Tricarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tricarboxylic acids and derivatives
• Alternative Parents: Alpha hydroxy acids and derivatives Tertiary alcohols Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tricarboxylic acid or derivatives - Hydroxy acid - Alpha-hydroxy acid - Tertiary alcohol - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.
• External Descriptors: tricarboxylic acid

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

Propriedades químicas e físicas

• Solubilidade: H 2 O: 1 M at 20 °C, clear, colorless
• Sensibilidade: Moisture sensitive
• Ponto de fusão (°C): 153-159°C
• Peso molecular: 192.120 g/mol
• XLogP3: -1.700
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 192.027 Da
• Monoisotopic Mass: 192.027 Da
• Topological Polar Surface Area: 132.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 227.000
• 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: 1