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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino L-Lactic Acid - Moligand™, ≥95%(T) , CAS No.79-33-4
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. ≥95%(T) 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
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥95%(T) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads 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.
Panoramica Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.
Specifications Sinonimi
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
Specifiche e purezza
Moligand™, ≥95%(T)
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C,Argon charged
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Sorrisi canonici
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
Isomeri SMILES
C[C@@H](C(=O)O)O
Gruppo di imballaggio
III
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720251&ln=
Documentazione 📋 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 Classe 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 Descrizione 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Solubilità Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide. Sensibilità Moisture & Light sensitive Indice di rifrazione 1.4260 to 1.4310 Rotazione specifica [α] -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.) Punto di infiammabilità (°C) 110 °C Punto di ebollizione (°C) 122 °C/20 hPa Punto di fusione (°C) 18 °C Peso molecolare 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
Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni 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 Recensioni 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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