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340,000+ prodotti di ricerca · Triple ISO certified · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino trans-10-Hydroxy-2-decenoic Acid - 10mM in DMSO , CAS No.14113-05-4
GRADE & PURITY 10mM in DMSO
Synonyms
(2E)-10-hydroxydec-2-enoic acid | Q16908844 | QHBZHVUGQROELI-SOFGYWHQSA-N | Silotermo Carmine G | trans-10-hydroxydec-2-enoic acid | DS-18448 | 10-Hydroxy-2-decylenic acid | (E)-10-Hydroxy-2-decenoic acid | AC-34577 | DTXSID601045504 | LMFA01050157 | Quee
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinonimi
(2E)-10-hydroxydec-2-enoic acid | Q16908844 | QHBZHVUGQROELI-SOFGYWHQSA-N | Silotermo Carmine G | trans-10-hydroxydec-2-enoic acid | DS-18448 | 10-Hydroxy-2-decylenic acid | (E)-10-Hydroxy-2-decenoic acid | AC-34577 | DTXSID601045504 | LMFA01050157 | Quee
Specifiche e purezza
10mM in DMSO
Meccanismi biochimici e fisiologici
VEGF inhibitor. Inhibits VEGF-induced angiogenesis. Suppresses VEGF-induced endothelial cell proliferation and migration. Promotes neurogenesis. Shows antiangiogenic, antioxidant and DNA-protective effects in vivo. Orally active.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Sorrisi canonici
C(CCCC=CC(=O)O)CCCO
IUPAC Name
(E)-10-hydroxydec-2-enoic acid
InChIKey
QHBZHVUGQROELI-SOFGYWHQSA-N
INCHI
1S/C10H18O3/c11-9-7-5-3-1-2-4-6-8-10(12)13/h6,8,11H,1-5,7,9H2,(H,12,13)/b8-6+
Isomeri SMILES
C(CCC/C=C/C(=O)O)CCCO
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1765264&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 Medium-chain hydroxy acids and derivatives Intermediate Tree Nodes Not available Direct Parent Medium-chain hydroxy acids and derivatives Alternative Parents Medium-chain fatty acids Hydroxy fatty acids Unsaturated fatty acids Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Medium-chain hydroxy acid - Medium-chain fatty acid - Hydroxy fatty acid - Straight chain fatty acid - Fatty acyl - Fatty acid - Unsaturated fatty acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound Descrizione This compound belongs to the class of organic compounds known as medium-chain hydroxy acids and derivatives. These are hydroxy acids with a 6 to 12 carbon atoms long side chain. 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.
Struttura 3D Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Sensibilità Heat sensitive Punto di fusione (°C) 64.0-68.0℃ Peso molecolare 186.250 g/mol XLogP3 2.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 8 Exact Mass 186.126 Da Monoisotopic Mass 186.126 Da Topological Polar Surface Area 57.500 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 152.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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