10-Hydroxydecanoic acid - 10mM in DMSO , CAS No.1679-53-4

CAS: 1679-53-4 Cat. No.: H422078 Molecular Weight: 188.26 EC Number: 216-848-1

GRADE & PURITY 10mM in DMSO

Synonyms

10-Hydroxydecanoic acid | 10-hydroxy-decanoic acid | CBU2X6BBJR | EN300-223806 | s5370 | 10-hydroxycapric acid | 10-Hydroxydecanoate;Decanoic acid, 10-hydroxy- | HY-Y0148 | MFCD00010510 | 10-HydroxydecanoicAcid | BCP21629 | (2R,3S)-rel-2,3-Dibromo-1,4-but

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonyms

10-Hydroxydecanoic acid | 10-hydroxy-decanoic acid | CBU2X6BBJR | EN300-223806 | s5370 | 10-hydroxycapric acid | 10-Hydroxydecanoate;Decanoic acid, 10-hydroxy- | HY-Y0148 | MFCD00010510 | 10-HydroxydecanoicAcid | BCP21629 | (2R, 3S)-rel-2, 3-Dibromo-1, 4-but

Specifications & Purity

10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

INHIBITOR

Names and Identifiers

• Canonical Smiles: C(CCCCC(=O)O)CCCCO
• IUPAC Name: 10-hydroxydecanoic acid
• InChIKey: YJCJVMMDTBEITC-UHFFFAOYSA-N
• INCHI: 1S/C10H20O3/c11-9-7-5-3-1-2-4-6-8-10(12)13/h11H,1-9H2,(H,12,13)
• Isomeric SMILES: C(CCCCC(=O)O)CCCCO
• WGK Germany: 3
• Molecular Weight: 188.26
• Reaxy-Rn: 1705390
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1705390&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Hydroxy acids and derivatives
      • Subclass Medium-chain hydroxy acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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 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 - 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
• Description: 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.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Hdac1 Histone deacetylase 1 (93 Activities)

Discover Target: Hdac1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HD1 Histone deacetylase (38 Activities)

Discover Target: HD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Melt Point(°C): 75.5-76.5°C
• Molecular Weight: 188.260 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 9
• Exact Mass: 188.141 Da
• Monoisotopic Mass: 188.141 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 123.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

References

1. Yuying Li, Junle Zhang, Yaxuan Shi, Yuancheng Zhang, Ge Shi, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Xiaoguang Qiao, Yanjie He, Yudong Wang, Haitao Zhao, Wenjie Zhang, Xinchang Pang.  (2023)  Robust Strategy to Improve the Compatibility between Incorporated Upconversion Nanoparticles and the Bulk Transparent Polymer Matrix.  ACS Omega,      [PMID:37692212] [10.1021/acsomega.3c04613]

2. 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]

3. Lu Chunxia, Tang Zonggui, Gao XiaoXu, Ma Xiaomei, Liu Changbin.  (2018)  Computer-aided design of magnetic dummy molecularly imprinted polymers for solid-phase extraction of ten phthalates from food prior to their determination by GC-MS/MS.  MICROCHIMICA ACTA,  185  (8): (1-11).  [PMID:30003399] [10.1007/s00604-018-2892-5]

4. Dan He, Yan Chen, Junfeng Shen, Han Yu, Jay D. Keasling, Xiaozhou Luo.  (2025)  Biosynthesis of 10-Hydroxy-2-Decenoic Acid in Escherichia coli.  METABOLIC ENGINEERING,      [PMID:39842502] [10.1016/j.ymben.2025.01.006]

5. 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]