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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque L-(-)-3-Phenyllactic acid - Moligand™, 10mM in DMSO , Agonist of HCA 3 receptor, CAS No.20312-36-1, Agonist of HCA 3 receptor
Disponível para encomenda
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. 10mM in DMSO Synonyms
(1S,9aR,11aS)-1-hydroxy-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-one | (R)-phenyllactate | KW7SNV9X8B | D-b-Phenyllactate | delta-3-Phenyllactate | GTPL12418 | (R)-a-Hydroxy-3-phenylpropionic acid | (
Shipped In
Dry ice packs + Cold packs
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Why this grade Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Visão geral L-(-)-3-Phenyllactic acid has been used in the development of degradable self-assembling depsipeptide nanofibers.
Specifications Sinónimos
(1S,9aR,11aS)-1-hydroxy-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-one | (R)-phenyllactate | KW7SNV9X8B | D-b-Phenyllactate | delta-3-Phenyllactate | GTPL12418 | (R)-a-Hydroxy-3-phenylpropionic acid | (
Especificações e pureza
Moligand™, 10mM in DMSO
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Mecanismo de ação
Agonist of HCA 3 receptor
Nomes e identificadores Sorrisos canónicos
C1=CC=C(C=C1)CC(C(=O)O)O
IUPAC Name
(2S)-2-hydroxy-3-phenylpropanoic acid
InChIKey
VOXXWSYKYCBWHO-QMMMGPOBSA-N
INCHI
1S/C9H10O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)/t8-/m0/s1
SMILES isoméricas
C1=CC=C(C=C1)C[C@@H](C(=O)O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2209791&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 Phenylpropanoids and polyketides Classe Phenylpropanoic acids Subclass Not available Intermediate Tree Nodes Not available Direct Parent Phenylpropanoic acids Alternative Parents Benzene and substituted derivatives Alpha hydroxy acids and derivatives Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents 3-phenylpropanoic-acid - Alpha-hydroxy acid - Monocyclic benzene moiety - Hydroxy acid - Benzenoid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound Descrição This compound belongs to the class of organic compounds known as phenylpropanoic acids. These are compounds with a structure containing a benzene ring conjugated to a propanoic acid. External Descriptors (2S)-2-hydroxy monocarboxylic acid - 3-phenyllactic 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.
Estrutura 3D Alvos associados (humanos) Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Rotação específica [α] -20.0 to -22.0 deg(C=2, H2O) Ponto de fusão (°C) 123-125°C Peso molecular 166.170 g/mol XLogP3 1.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 166.063 Da Monoisotopic Mass 166.063 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 150.000 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
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Reconstitution Calculator Revisões 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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