Sodium DL-lactate solution - BioReagent, synthetic, syrup, suitable for mouse embryo cell culture, 60 % (w/w) , CAS No.72-17-3

CAS: 72-17-3 Cat. No.: S755695 Formula: C₃H₅NaO₃ Peso molecolare: 112.06 Beilstein Registry Number: 4332999 Numero EC: 200-772-0 PubChem CID: 23666456

GRADE & PURITY BioReagent, synthetic, syrup, suitable for mouse embryo cell culture, 60 % (w/w)

Storage

Store at 2-8°C

Shipped In

Wet ice

Panoramica

Lactic acid is an α hydroxyl carboxylic acid produced from pyruvate by the enzyme lactate dehydrogenase (LDH). This mixed isomer lactate has been qualified for use in mouse embryo culture. Lactate regulates pyruvate uptake and metabolism in the preimplantation mouse embryo.

Specifications

Specifiche e purezza

BioReagent, synthetic, syrup, suitable for mouse embryo cell culture, 60 % (w/w)

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

BioReagent

Nomi e identificatori

• Sorrisi canonici: CC(C(=O)[O-])O.[Na+]
• IUPAC Name: sodium;2-hydroxypropanoate
• InChIKey: NGSFWBMYFKHRBD-UHFFFAOYSA-M
• INCHI: 1S/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1
• Isomeri SMILES: CC(C(=O)[O-])O.[Na+]
• WGK Germania: 2
• PubChem CID: 23666456
• Peso molecolare: 112.06
• Beilstein: 4332999

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid salts
• Alternative Parents: Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - Carboxylic acid salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organic zwitterion - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acid salts. These are ionic derivatives of carboxylic acid.
• External Descriptors: organic sodium salt - lactate salt

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

Proprietà chimiche e fisiche

• Indice di rifrazione: 1.422-1.425
• Peso molecolare: 112.060 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 112.014 Da
• Monoisotopic Mass: 112.014 Da
• Topological Polar Surface Area: 60.400 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 63.200
• 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

XLogP3

Riferimenti

1. Xue-Meng Wang, Zhi-Xuan Zhang, Lin Chen, Rong Chen, Wen-Wei Li.  (2025)  Crystal facet optimization in cadmium sulfide/reduced graphene oxide-based photosynthetic biohybrid systems for enhanced light-driven biohydrogen production.  BIORESOURCE TECHNOLOGY,      [PMID:40692070] [10.1016/j.biortech.2025.133017]

2. Cheng Guoqing, Ding Huili, Chen Guanglin, Shi Hongjie, Zhang Xu, Zhu Minglong, Tan Wensong.  (2022)  Effects of cadmium sulfide nanoparticles on sulfate bioreduction and oxidative stress in Desulfovibrio desulfuricans.  Bioresources and Bioprocessing,  9  (1): (1-15).  [PMID:38647594] [10.1186/s40643-022-00523-5]

3. Zhang Jia, Guo Lu-Yao, Lin Xiao-Qian, Wen Gui-Hua, Zhang Xue-Feng, Yu Li-Hong, He Mei-Qian, He Yu-Mei, Zou Long, Zhang Meng-Tian, Cao Li-Ming, He Chun-Ting.  (2025)  Microbial-vulcanized organic-inorganic dual-modulated cobalt hydroxide for oxygen evolution reaction.  Nature Communications,  16  (1): (10766).  [PMID:41315433] [10.1038/s41467-025-65807-8]

4. Jing Zhao, Nuo Zhang, Lingfeng Qin, Jingjing Liu, Jing Wang, Yuanfang Xiang, Jiao Zhang, Qingwei Meng, Yong Huang, Chen Lin, Jing Zhao, Xiuxiu Wang, Wei Wei.  (2026)  Reprogramming bacterial energetics reverses lactate-mediated immunosuppression for synergistic cancer immunotherapy.  TRENDS IN BIOTECHNOLOGY,      [PMID:42315363] [10.1016/j.tibtech.2026.05.021]