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Sodium citrate monobasic - BioReagent, anhydrous, ≥99.5%(T), high purity , CAS No.18996-35-5
Basic Description
Specifications & Purity
BioReagent, anhydrous, ≥99.5%(T)
Storage Temp
Room temperature
Shipped In
Normal
Grade
anhydrous, BioReagent
Product Description
Sodium citrate monobasic has been used-as a component of Beltsville thawing solution (BTS) for semen dilution for the formulation of isonitrogenous diets to study the effects of sodium citrate in red hybrid tilapia for the preparation of SSC (saline sodium citrate) made for post-hybridization wash
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Carboxylic acids and derivatives
Subclass
Tricarboxylic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Tricarboxylic acids and derivatives
Alternative Parents
Tertiary alcohols Carboxylic acid salts Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Tricarboxylic acid or derivatives - Tertiary alcohol - Carboxylic acid salt - Organic alkali metal salt - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
Description
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
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.
Names and Identifiers
PH
3.5-4.0 (25 °C, 0.25 M in H 2 O)
IUPAC Name
sodium;3-carboxy-3,5-dihydroxy-5-oxopentanoate
INCHI
InChI=1S/C6H8O7.Na/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);/q;+1/p-1
InChIKey
HWPKGOGLCKPRLZ-UHFFFAOYSA-M
Smiles
C(C(=O)O)C(CC(=O)[O-])(C(=O)O)O.[Na+]
Isomeric SMILES
C(C(=O)O)C(CC(=O)[O-])(C(=O)O)O.[Na+]
WGK Germany
1
RTECS
GE7950000
PubChem CID
23666341
Molecular Weight
214.11
Beilstein
3920246
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
H 2 O: 0.25 M at 20 °C, clear, colorless
Melt Point(°C)
209-215°C
Molecular Weight
214.100 g/mol
XLogP3
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
5
Exact Mass
214.009 Da
Monoisotopic Mass
214.009 Da
Topological Polar Surface Area
135.000 Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
251.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
2
Citations of This Product
1.
Juncong Zou, Xiang Li, Shanying He, Qiuya Niu, Shaohua Wu, Chunping Yang.
(2024)
Atomically Permeated MoP-WOx Core-Shell Catalysts for Efficient and Selective Oxidation of Thiophenic Sulfides in Fuels via Direct Electron Transfer Mechanism. ADVANCED FUNCTIONAL MATERIALS,
(2415558).
2.
Zhiqing Hu, Li Zhang, Lili Ren, Jiang Zhou.
(2025)
Broadband and omnidirectional antireflective coatings with gradient refractive index prepared using chitin nanofibers and pore generation agent. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,
302
(140517).
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2 Citations