Basic information
- CAS
624-00-0- Standard SMILES
CCCCCC(O)CCCC(=O)O- InChIKey
LMHJFKYQYDSOQO-UHFFFAOYSA-N- Molecular formula
- C10H20O3
- Average molar mass
- 188.26 g/mol
- Monoisotopic mass
- 188.1412445
Overview
5-Hydroxycapric acid is a medium-chain fatty acid. It is a conjugate acid of a 5-hydroxydecanoate.
Names & identifiers
- Preferred name
- 5-Hydroxydecanoic acid
- IUPAC
- 5-hydroxydecanoic acid
- English name
- 5-Hydroxydecanoic acid sodium salt
- Molecular formula
- C10H20O3
- Molecular weight
- 188.26
Names & synonyms
5-HYDROXYDECANOIC ACID624-00-0DTXSID10977956RefChem:913445DTXCID601405287Decanoic acid, 5-hydroxy-5-hydroxy capric acidM-141575-Hydroxycapric acidxi-5-Hydroxydecanoic acidLopac0_000628BSPBio_001564
Show more names
5-hydroxydecanoate sodium salt5-HYDROXYDECANOIC ACID SODIUM SALT WHITE SOLID
KBioGR_000284KBioSS_000284SCHEMBL316603orb2567335orb2901316CHEMBL1373782KBio2_000284KBio2_002852
Database identifiers
- CAS
624-00-0- PubChem CID
- 1825
- DTXSID
DTXSID10977956- ChEMBL
CHEMBL1373782- ChEBI
CHEBI:165412- Nikkaji
- J262.022G
Properties
Computed structural properties
- XLogP
- 2.2
- Topological polar surface area
- 57.5 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 8
- Heavy atoms
- 13
- Formal charge
- 0
- Complexity
- 134
Experimental & physicochemical properties
LipidsFatty Acyls [FA] -> Fatty Acids and Conjugates [FA01] -> Hydroxy fatty acids [FA0105]
Physicochemical properties
- Melting point
- 155 · 155-157°C
- storage temp.
- Refrigerator
- solubility
- 2 O: · H2O: soluble
- form
- solid
- color
- white
- LogP
- 1.84 · 1.840 (est)
- WGK Germany
- 3 · 3
Safety & regulation
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
Safety data
- wgk
- 3
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.
Cellular LocationsCytoplasm
Applications
UsesA potassium channel antagonist which blocks the postischemic effects of the potassium channel activator cromakalim
Suppliers13 total
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
山东西亚化学有限公司13355009207 13355009207 · [email protected]
金瓯生物医药（南京）有限公司13000000000 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
成都卡麦尔医药科技有限公司028-67136579 15828051124 · [email protected]
Alfa Chemistry+1-5166625404 · [email protected]
杭州洁汉化工有限公司+86-571-86217390; +8618058761490 · [email protected]
Related reactions
1 records
Compound notes
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