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Details

Stereochemistry ACHIRAL
Molecular Formula C14H31N
Molecular Weight 213.4026
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRISTYLAMINE

SMILES

CCCCCCCCCCCCCCN

InChI

InChIKey=PLZVEHJLHYMBBY-UHFFFAOYSA-N
InChI=1S/C14H31N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-15H2,1H3

HIDE SMILES / InChI

Molecular Formula C14H31N
Molecular Weight 213.4026
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Triggered instability of liposomes bound to hydrophobically modified core-shell PNIPAM hydrogel beads.
2010-01-19
Reaction of alkylamine surfactants with carbon dioxide: relevance to nanocrystal synthesis.
2009-05
Hierarchical assembly of ultranarrow alkylamine-coated ZnS nanorods: a synchrotron surface X-ray diffraction study.
2008-11
Anaerobic degradation of long-chain alkylamines by a denitrifying Pseudomonas stutzeri.
2008-10
Conductometric study of antidepressant drug-cationic surfactant mixed micelles in aqueous solution.
2008-06-15
Substrate specificity of a long-chain alkylamine-degrading Pseudomonas sp isolated from activated sludge.
2008-02
Development of a new C14 monolithic silica column containing embedded polar groups for pressurized capillary electrochromatography.
2007-11
Use of a pH-sensitive fluorescent probe for measuring intracellular pH of Caco-2 cells.
2007-06-29
Simultaneous determination of neomycin sulfate and polymyxin B sulfate by capillary electrophoresis with indirect UV detection.
2007-02-19
Ion-selective electrodes for determination of organic ammonium ions: Ways for selectivity control.
2006-12-15
Synthesis and mechanism study of mesoporous SnO2/SiO2 composites.
2006-07
Structure-function relations of carbohydrates by neoglycolipid arrays.
2006-06
Fabrication and application of neoglycolipid arrays in a microtiter plate.
2006-04-01
In vitro activity of lauric acid or myristylamine in combination with six antimicrobial agents against methicillin-resistant Staphylococcus aureus (MRSA).
2006-01
Antimicrobial activity of saturated fatty acids and fatty amines against methicillin-resistant Staphylococcus aureus.
2004-09
NMR studies of restricted diffusion in lyotropic systems.
2002-12-10
Characterization of solvation properties of lipid bilayer membranes in liposome electrokinetic chromatography.
2002-10-11
Arachidonic acid-induced H+ and Ca2+ increases in both the cytoplasm and nucleoplasm of rat cerebellar granule cells.
2001-12-01
Simultaneous determination of ingredients in an ointment by hydrophobic interaction electrokinetic chromatography.
2001-09-21
On-line concentration of s-triazine herbicides in micellar electrokinetic chromatography using a cationic surfactant.
2001-05-04
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:53:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:53:28 GMT 2025
Record UNII
NOM20L9LFT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-66437
Preferred Name English
MYRISTYLAMINE
Systematic Name English
TETRADECYLAMINE
Systematic Name English
1-TETRADECYLAMINE
Systematic Name English
1-AMINOTETRADECANE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
217-950-9
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
NSC
66437
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
PUBCHEM
16217
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
FDA UNII
NOM20L9LFT
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID9040768
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
MESH
C020514
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
CAS
2016-42-4
Created by admin on Mon Mar 31 18:53:28 GMT 2025 , Edited by admin on Mon Mar 31 18:53:28 GMT 2025
PRIMARY
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY