Sodium DL-lactate solution - 73% in water , CAS No.72-17-3

CAS: 72-17-3 Cat. No.: S301759 Summenformel: C₃H₅NaO₃ Molekulargewicht: 112.06 Beilstein Registry Number: 4332999 EG-Nummer: 200-772-0 PubChem CID: 23666456

GRADE & PURITY 73% in water

Synonyms

Sodium 2-Hydroxypropionate | 2-hydroxypropionic acid sodium salt | DL-Lactic acid sodium salt

Storage

Store at 2-8°C

Shipped In

Wet ice

Übersicht

Sodium DL-lactate is an organic, sodium salt of lactic acid. It is a hygroscopic agent and a component of natural moisturizing factor (NMF). It is usually produced by fermentation. 

Application 

Sodium DL-lactate has been used as a component in Trypticase soy broth to culture P. gingivalis and to observe prolonged methane production in batch assays.

Specifications

Synonyme

Sodium 2-Hydroxypropionate | 2-hydroxypropionic acid sodium salt | DL-Lactic acid sodium salt

Spezifikationen & Reinheit

73% in water

Biochemische und physiologische Mechanismen

Biochem/physiol Actions Sodium lactate functions as a buffer to maintain osmotic and charge balance. It serves as a humectant, especially in cosmetic preparations. It acts a flavoring agent in meat and poultry products. Sodium lactate also plays a role as

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

• Pubchem Sid: 504769528
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769528
• Kanonisches Lächeln: 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
• Isomere SMILES: CC(C(=O)[O-])O.[Na+]
• WGK Deutschland: 2
• PubChem CID: 23666456
• Molekulargewicht: 112.06
• Beilstein: 4332999

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Zugehörige Ziele (menschlich)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

Discover Target: CA5A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

Discover Target: CA9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Homo sapiens (32628 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

Discover Target: SLC16A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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CA4 Carbonic anhydrase IV (1713 Activities)

Discover Target: CA4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HD1 Histone deacetylase (38 Activities)

Discover Target: HD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.422-1.425
• Molekulargewicht: 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

Referenzen

1. 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]

2. 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]

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]