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· · COA & SDS available for every product · Same-day shipping on in-stock items L-Lactic Acid - Moligand™, ≥80% , Agonist of HCA 1 receptor, CAS No.79-33-4, Agonist of HCA 1 receptor
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥80% Synonyms
L-(+)-Lactic acid, BioXtra, >=98% (titration) | L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | L-(+)-Lactic acid 95% liquid | LACTIC ACID, L-(II) | (S)-LACTIC ACID [EP MONOGRAPH] | 1-Hydroxyethane 1-c
Storage
Store at 2-8°C,Argon charged
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Why this grade Moligand™, ≥80% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 123 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.
Specifications Synonyms
L-(+)-Lactic acid, BioXtra, >=98% (titration) | L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | L-(+)-Lactic acid 95% liquid | LACTIC ACID, L-(II) | (S)-LACTIC ACID [EP MONOGRAPH] | 1-Hydroxyethane 1-c
Specifications & Purity
Moligand™, ≥80%
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Agonist of HCA 1 receptor
Names and Identifiers Pubchem Sid 508810630 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/508810630 Canonical Smiles C[C@H](O)C(O)=O IUPAC Name (2S)-2-hydroxypropanoic acid InChIKey JVTAAEKCZFNVCJ-REOHCLBHSA-N INCHI 1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1 Isomeric SMILES C[C@@H](C(=O)O)O WGK Germany 1 RTECS OD2800000 UN Number 3265 Packing Group III Molecular Weight 90.08 Beilstein 1720251 Reaxy-Rn 1720251 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720251&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Class Hydroxy acids and derivatives Subclass Alpha hydroxy acids and derivatives Intermediate Tree Nodes Not available Direct Parent Alpha hydroxy acids and derivatives Alternative Parents Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Alpha-hydroxy acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as alpha hydroxy acids and derivatives. These are organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon. External Descriptors 2-hydroxypropanoic 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide. Sensitivity Moisture & Light sensitive x_refractive_index 1.4260 to 1.4310 x_specific_rotation -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.) x_flash_point_drop_centigrade 110 °C x_boil_point_char 122 °C/20 hPa x_melt_point_char 18 °C Molecular Weight 90.080 g/mol XLogP3 -0.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 90.0317 Da Monoisotopic Mass 90.0317 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 6 Formal Charge 0 Complexity 59.100 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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
FAQs and Articles Citations of This Product Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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