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544-63-8 molecular structure
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tetradecanoic acid

ChemBase ID: 5856
Molecular Formular: C14H28O2
Molecular Mass: 228.37092
Monoisotopic Mass: 228.20893014
SMILES and InChIs

SMILES:
C(=O)(O)CCCCCCCCCCCCC
Canonical SMILES:
CCCCCCCCCCCCCC(=O)O
InChI:
InChI=1S/C14H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3,(H,15,16)
InChIKey:
TUNFSRHWOTWDNC-UHFFFAOYSA-N

Cite this record

CBID:5856 http://www.chembase.cn/molecule-5856.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
tetradecanoic acid
IUPAC Traditional name
myristic acid
Synonyms
MYRISTIC ACID
C14:0 (Lipid numbers)
1-Tridecanecarboxylic acid
C14:0
NSC 5028
Myristic acid
Tetradecanoic acid
Myristic acid
Tetradecanoic acid
tetradecanoic acid
十四烷酸
肉豆蔻酸
十四烷酸
CAS Number
544-63-8
EC Number
208-875-2
MDL Number
MFCD00002744
Beilstein Number
508624
Merck Index
146333
PubChem SID
99444702
24886048
160969283
24901314
24886049
24901313
24896795
PubChem CID
11005
CHEMBL
111077
Chemspider ID
10539
FEMA ID
2764
Wikipedia Title
Myristic_acid
Council of Europe Number
16
Flavis Number
8.016

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 4.9520197  H Acceptors
H Donor LogD (pH = 5.5) 4.71164 
LogD (pH = 7.4) 2.9525049  Log P 5.3674455 
Molar Refractivity 67.8816 cm3 Polarizability 27.025951 Å3
Polar Surface Area 37.3 Å2 Rotatable Bonds 12 
Lipinski's Rule of Five false 
Log P 6.1  LOG S -5.12 
Solubility (Water) 1.72e-03 g/l 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
Melting Point
52-54 °C(lit.) expand Show data source
53-56 °C expand Show data source
53-56°C expand Show data source
54.4 °C expand Show data source
54.5 °C expand Show data source
54.5°C expand Show data source
Boiling Point
250 °C/100 mmHg(lit.) expand Show data source
250.5 °C at 100 mmHg expand Show data source
326°C expand Show data source
326°C expand Show data source
ca. 326 °C at 1013 hPa expand Show data source
Flash Point
>113 °C expand Show data source
>235.4 °F expand Show data source
175°C(347°F) expand Show data source
ca. 175 °C (Cleveland Open Cup) expand Show data source
Density
0.862 expand Show data source
0.8622 g/cm3 expand Show data source
ca. 858 kg/m3 at 60 °C expand Show data source
Vapor Pressure
.0065 hPa at 20 °C expand Show data source
Hydrophobicity(logP)
6.154 expand Show data source
Organoleptic
oily; waxy expand Show data source
Storage Condition
0°C expand Show data source
RTECS
QH4375000 expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
nwg expand Show data source
Risk Statements
36/37/38 expand Show data source
38 expand Show data source
R:36/37/38 expand Show data source
Safety Statements
26-37 expand Show data source
S:20-25-26-37/39 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315 expand Show data source
H315-H319-H335 expand Show data source
H319 expand Show data source
GHS Precautionary statements
P261-P305+P351+P338-P302+P352-P321-P405-P501A expand Show data source
P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Storage Temperature
-20°C expand Show data source
Regulation Compliance
EU Regulation 1334/2008 & 178/2002 expand Show data source
FCC expand Show data source
FDA 21 CFR (172.210) expand Show data source
FDA 21 CFR (172.860) expand Show data source
FDA 21 CFR (173.340) expand Show data source
Allergens
no known allergens expand Show data source
Purity
~95% expand Show data source
≥98.0% (GC) expand Show data source
≥98.5% (GC) expand Show data source
≥99% expand Show data source
≥99.5% expand Show data source
≥99.5% (GC) expand Show data source
95% expand Show data source
95+% expand Show data source
98% expand Show data source
99-100% expand Show data source
Grade
analytical standard expand Show data source
certified reference material expand Show data source
FG expand Show data source
Halal expand Show data source
Kosher expand Show data source
natural expand Show data source
NI expand Show data source
Sigma Grade expand Show data source
TECHNICAL expand Show data source
Certificate of Analysis
Download expand Show data source
Download expand Show data source
Download expand Show data source
Packaging
pkg of 1 g expand Show data source
Shelf Life
(limited shelf life, expiry date on the label) expand Show data source
Pharmacopeia Traceability
traceable to USP 1448990 expand Show data source
Linear Formula
CH3(CH2)12COOH expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals DrugBank DrugBank Sigma Aldrich Sigma Aldrich Wikipedia Wikipedia
MP Biomedicals - 02102375 external link
Technical Grade
Purity: ~95%
Crystalline
MP Biomedicals - 02100870 external link
Crystalline
Purity: 99-100%
MP Biomedicals - 05216758 external link
MP Biomedicals Rare Chemical collection
DrugBank - DB08231 external link
Drug information: experimental
Sigma Aldrich - 153796 external link
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - PHR1124 external link
General description
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO Guide 34.
Other Notes
Values of analytes vary lot to lot.
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - W276405 external link
Packaging
1 kg in poly bottle
5, 10 kg in poly drum
1 sample in glass bottle
100 g in poly bottle
25 kg in fiber drum
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - 130087 external link
Packaging
1 kg in poly bottle
5 g in glass bottle
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - 70079 external link
Other Notes
Binding to serum albumin2
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - M3128 external link
Biochem/physiol Actions
Myristic acid is a straight-chain 14-carbon fatty acid. Diets rich in myristic acid, along with lauric and palmitic acids, are associated with increased serum levels of low densisity lipoprotein cholesterol.
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
包装
10, 100, 500 g in poly bottle
Sigma Aldrich - W276413 external link
Packaging
1 kg in poly bottle
1 sample in glass bottle
5, 10, 25 kg in fiber drum
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - 70080 external link
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.
Sigma Aldrich - 70082 external link
Biochem/physiol Actions
Myristic acid is commonly added via a covalent linkage to the N-terminal glycine of many eukaryotic and viral proteins, a process called myristoylation. Myristoylation enables proteins to bind to cell membranes and facilitates protein-protein interactions. Myristolyation of proteins affect many cellular functions and thus has implications in health and disease 1.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

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