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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items DL-3-Hydroxybutyric Acid (contains Polymolecular esterification product) - Moligand™, 10mM in DMSO , Agonist of HCA 2 receptor, CAS No.300-85-6, Agonist of HCA 2 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. 10mM in DMSO Synonyms
3-hydroxybutyric acid|3-hydroxybutanoic acid|300-85-6|Butanoic acid, 3-hydroxy-|beta-Hydroxybutyric acid|625-71-8|3 HBA|DL-3-Hydroxybutyric Acid|3-Hydroxybuttersaeure|Butyric acid, 3-hydroxy-|DL-beta-Hydroxybutyric acid|beta-Hydroxybuttersaeure|beta-hydro
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.
Descripción general 3-Hydroxybutyric acid was used in enantioselective synthesis of D-(-)-3-hydroxybutyric acid by Escherichia coli
Specifications Sinónimos
3-hydroxybutyric acid | 3-hydroxybutanoic acid | 300-85-6 | Butanoic acid, 3-hydroxy- | beta-Hydroxybutyric acid | 625-71-8 | 3 HBA | DL-3-Hydroxybutyric Acid | 3-Hydroxybuttersaeure | Butyric acid, 3-hydroxy- | DL-beta-Hydroxybutyric acid | beta-Hydroxybuttersaeure | beta-hydro
Especificaciones y pureza
Moligand™, 10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Agonist of HCA 2 receptor
Nombres e identificadores Sonrisas canónicas CC(CC(=O)O)O IUPAC Name 3-hydroxybutanoic acid InChIKey WHBMMWSBFZVSSR-UHFFFAOYSA-N INCHI 1S/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7) Isómeros SMILES CC(CC(=O)O)O Peso molecular 104.11 Beilstein 3307 Reaxy-Rn 773861 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773861&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 Clase Hydroxy acids and derivatives Subclass Beta hydroxy acids and derivatives Intermediate Tree Nodes Not available Direct Parent Beta hydroxy acids and derivatives Alternative Parents Short-chain hydroxy acids and derivatives Fatty acids and conjugates Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Short-chain hydroxy acid - Beta-hydroxy acid - Fatty 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 Descripción This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom. External Descriptors Hydroxy fatty acids 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Hygroscopic,Heat Sensitive Peso molecular 104.100 g/mol XLogP3 -0.500 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 104.047 Da Monoisotopic Mass 104.047 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 7 Formal Charge 0 Complexity 69.300 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 1
Citations of This Product Referencias 1. Shendong Zhou, Mengru Chen, Meijuan Meng, Nana Ma, Wan Xie, Xiangzhen Shen, Zhixin Li, Guangjun Chang. (2023) Subclinical ketosis leads to lipid metabolism disorder by down-regulating the expression of Acetyl-CoA acetyltransferase 2 (ACAT2) in dairy cows. JOURNAL OF DAIRY SCIENCE, [PMID:37690731 ] [10.3168/jds.2023-23602 ]
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