trans-10-Hydroxy-2-decenoic Acid - 10mM in DMSO , CAS No.14113-05-4

CAS: 14113-05-4 Cat. No.: T421529 Peso molecular: 186.25 Número EC: 808-119-7
Disponible para pedir
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
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
T421529-1ml
1

58,90US$

69,90US$
Guardar 11,00 US$ (15.74%)
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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.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
(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
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
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.
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.
Nombres e identificadores
Sonrisas canónicasC(CCCC=CC(=O)O)CCCO
IUPAC Name(E)-10-hydroxydec-2-enoic acid
InChIKeyQHBZHVUGQROELI-SOFGYWHQSA-N
INCHI1S/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+
Isómeros SMILES C(CCC/C=C/C(=O)O)CCCO
Peso molecular 186.25
Reaxy-Rn 1765264
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1765264&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseHydroxy acids and derivatives
SubclassMedium-chain hydroxy acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentMedium-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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadHeat sensitive
Punto de fusión (°C)64.0-68.0℃
Peso molecular186.250 g/mol
XLogP32.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count8
Exact Mass186.126 Da
Monoisotopic Mass186.126 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count13
Formal Charge0
Complexity152.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Shixuan Su, Shanshan Li, Jing Hu, Ting Yu, Lingchen Tao, Fuliang Hu, Yunlei Xianyu.  (2021)  A colorimetric sensing strategy for detecting 10-hydroxy-2-decenoic acid in royal jelly based on Ag(I)-tetramethylbenzidine.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2021.131241]
2. Shuai Zhuang, Huihui Ming, Wenjie Yu, Liping Luo.  (2024)  Identification of freshness and metabolite changes of royal jelly during storage using Nano-ESI-MS and UPLC-Q/TOF-MS.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.107092]
3. Xinqi Huang, Lu Xiu, Yumei An, Yuan Gong, Sunao Li, Xueshi Chen, Chao Liu, Jianghuiwen Lu, Haiyan Shan, Jie Chang, Mingyang Zhang.  (2024)  Preventive Effect of Royal Jelly and 10-HDA on Skin Damage in Diabetic Mice through Regulating Keratinocyte Wnt/β-Catenin and Pyroptosis Pathway.  MOLECULAR NUTRITION & FOOD RESEARCH,  68  (19): (2400098).  [PMID:39246232] [10.1002/mnfr.202400098]
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