Basic information
- Standard SMILES
O=C(O)CCCCCCCCCCCCCCO- InChIKey
BZUNJUAMQZRJIP-UHFFFAOYSA-N- Molecular formula
- C15H30O3
- Average molar mass
- 258.4 g/mol
- Monoisotopic mass
- 258.21949481
Names & identifiers
- Preferred name
- 15-Hydroxypentadecanoic acid
- IUPAC
- 15-hydroxypentadecanoic acid
- English name
- 15-Hydroxypentadecanoic acid
- Molecular formula
- C15H30O3
- Molecular weight
- 258.4
Names & synonyms
Show more names
Database identifiers
- CAS
4617-33-8- PubChem CID
- 78360
- DTXSID
DTXSID00196750- ChEBI
CHEBI:79169- UNII
- FU65P3692T
- EC Number
- 225-026-1
- Nikkaji
- J208.609C
Properties
Computed structural properties
- XLogP
- 4.2
- Topological polar surface area
- 57.5 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 14
- Heavy atoms
- 18
- Formal charge
- 0
- Complexity
- 181
Physicochemical properties
- Melting point
- 85 · 85-89 °C(lit.)
- Boiling point
- 174 · 174-220 °C(Press: 4 Torr)
- Density
- 0.963 · 0.963±0.06 g/cm3(Predicted)
- storage temp.
- 2 · 2-8°C
- solubility
- Chloroform (Slightly, Sonicated), DMSO (Slightly)
- pka
- 4.78 · 4.78±0.10(Predicted)
- form
- Solid
- color
- White to Off-White
- BRN
- 1240100 · 1240100
- InChI
- InChI=1S/C15H30O3/c16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15(17)18/h16H,1-14H2,(H,17,18)
- InChIKey
- BZUNJUAMQZRJIP-UHFFFAOYSA-N
- SMILES
- C(O)(=O)CCCCCCCCCCCCCCO
- CAS DataBase Reference
- 4617 · 4617-33-8(CAS DataBase Reference)
- FDA UNII
- 65 P3692T · FU65P3692T
- UNSPSC Code
- 12352100 · 12352100
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319
- Precautionary statements
- 264 · P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- PPE
- 95 · Eyeshields, Gloves, type N95 (US)
- Hazard Codes
- Xi
- Safety Statements
- 24 · 24/25
- WGK Germany
- 3 · 3
- Hazard Note
- Irritant
- HS Code
- 2915907098 · 2915907098
- Storage Class
- 11 · 11 - Combustible Solids
Safety & regulation
GHS classification
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation];H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364 (click each P-code to see the statement)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Hazard information
Safety data
- PPE
- Eyeshields, Gloves, type N95 (US)
- wgk
- 3
- hs_code
- 2915907098
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- hazard_note
- Irritant
- safety_code
- 24/25
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H319
- Precautionary statements
- P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Chemistry & industry
Applications
Description15-hydroxy Pentadecanoic acid is a hydroxylated fatty acid that has been used in the synthesis of the macrocyclic lactone musk compounds exaltolide and phoracantholide I. [Matreya, LLC. Catalog No. 1881]
Uses15-Hydroxypentadecanoic acid is suitable reagent used in the following studies: As an internal standard in the quantification of formation of 11-hydroxylauric acid by gas chromatography.In the synthesis of [16-14C]16DCA (DCA= dicarboxylic acid) by one-carbon elongation procedure at C15.As an internal standard for the normalization of intensities in the mass spectra of plant cutin polymer.It may be used in the synthesis of 5-pentadecanolide on dealuminated HY zeolite and also fatty acid analog of podophyllotoxin.
General Description15-Hydroxypentadecanoic acid undergoes lactonization reaction catalyzed by Mucor javanicus L46 and Mucor miehei to afford macrocyclic mono- and oligolactone derivatives. Its lipase-catalyzed synthesis from 15-tetracosenoic acid in Malania Olcifera Chum oil has been proposed. It also participates in the biosynthesis of pentadecanolide.
Upstream & downstream products
Downstream products
Suppliers50 total
Additional notes
DefinitionChEBI: An omega-hydroxy fatty acid that is pentadecanoic acid in which one of the hydrogens of the terminal methyl group has been replaced by a hydroxy group.
Related reactions
Linked notes
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