To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Tridecylic acid

From Wikipedia, the free encyclopedia

Tridecylic acid
Skeletal formula of tridecylic acid
Ball-and-sitck model of tridecylic acid
Names
Preferred IUPAC name
Tridecanoic acid
Other names
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.010.311 Edit this at Wikidata
EC Number
  • 211-341-1
RTECS number
  • YD3850000
UNII
  • InChI=1S/C13H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13(14)15/h2-12H2,1H3,(H,14,15) checkY
    Key: SZHOJFHSIKHZHA-UHFFFAOYSA-N checkY
  • O=C(O)CCCCCCCCCCCC
Properties
C13H26O2
Molar mass 214.349 g·mol−1
Appearance White crystals or powder
Odor Waxy-type
Density 0.983 g/cm3 (37 °C)[1]
0.8458 g/cm3 (80 °C)[2]
Melting point 41.5 °C (106.7 °F; 314.6 K)[2]
Boiling point 236 °C (457 °F; 509 K)
at 100 mmHg
140 °C (284 °F; 413 K)
at 1 mmHg[2]
21 mg/L (0 °C)
33 mg/L (20 °C)
38 mg/L (30 °C)
53 mg/L (60 °C)[3]
Solubility Soluble in alcohol, ether, CH3COOH[2]
Solubility in acetone 7.52 g/100 g (0 °C)
78.6 g/100 g (20 °C)
316 g/100 g (30 °C)
8.23 kg/100 g (40 °C)[3]
Solubility in methanol 12.6 g/100 g (0 °C)
148 g/100 g (20 °C)
515 g/100 g (30 °C)[3]
Solubility in benzene 42.4 g/100 g (10 °C)
117 g/100 g (20 °C)
354 g/100 g (30 °C)[3]
Solubility in ethyl acetate 10.1 g/100 g (0 °C)
70 g/100 g (20 °C)
281 g/100 g (30 °C)[3]
Vapor pressure 0.01 kPa (109 °C)
0.47 kPa (160 °C)
3.21 kPa (200 °C)[4]
100 kPa (311.5 °C)[2]
1.4286 (50 °C)[2]
Viscosity 0.583 cP (120 °C)
0.3991 cP (160 °C)
0.2934 cP (200 °C)[5]
Structure
Monoclinic (37 °C)[1]
C2/c[1]
a = 59.88 Å, b = 4.9425 Å, c = 9.8118 Å[1]
α = 90°, β = 93.8°, γ = 90°
Thermochemistry
387.6 J/mol·K[4]
−807.2 kJ/mol (liquid)[4]
8024.2 kJ/mol (liquid)[4]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Irritant
GHS labelling:
GHS07: Exclamation mark[6]
Warning
H315, H319, H335[6]
P261, P305+P351+P338[6]
NFPA 704 (fire diamond)
[7]
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Flash point 113 °C (235 °F; 386 K)[6]
Lethal dose or concentration (LD, LC):
130 mg/kg (mice, intravenous)[7]
Related compounds
Related compounds
 Dodecanoic acid, Tetradecanoic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Tridecylic acid, or tridecanoic acid, is the organic compound with the formula CH3(CH2)11CO2H. It is a 13-carbon saturated fatty acid. It is a white solid.

A laboratory preparation involves permanganate oxidation of 1-tetradecene (CH3(CH2)12CH=CH2).[8]

YouTube Encyclopedic

  • 1/3
    Views:
    391
    452
    27 338
  • Myristic acid Meaning
  • 3D molecular structure of Myristic acid ( a common saturated fatty acid )
  • Fatty Acid Synthesis (Part 5 of 12) - Palmitate Synthesis

Transcription

See also

References

  1. ^ a b c d Bond, Andrew D. (2003). "On the crystal structures and melting point alternation of the n-alkyl carboxylic acids" (PDF). rsc.org. Royal Society of Chemistry. Retrieved 2014-06-15.
  2. ^ a b c d e f Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
  3. ^ a b c d e Seidell, Atherton; Linke, William F. (1940). Solubilities of Inorganic and Organic Compounds (3rd ed.). New York: D. Van Nostrand Company. p. 756.
  4. ^ a b c d Tridecanoic acid in Linstrom, Peter J.; Mallard, William G. (eds.); NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg (MD) (retrieved 2014-06-17)
  5. ^ Yaws, Carl L. (2009). Transport Properties of Chemicals and Hydrocarbons. New York: William Andrew Inc. p. 174. ISBN 978-0-8155-2039-9.
  6. ^ a b c d Sigma-Aldrich Co., Tridecanoic acid. Retrieved on 2014-06-17.
  7. ^ a b "MSDS of n-Tridecanoic acid". fishersci.ca. Fisher Scientific. Retrieved 2014-06-17.
  8. ^ Lee DG, Lamb SE, Chang VS (1981). "Carboxylic Acids from the Oxidation of Terminal Alkenes by Permanganate: Nonadecanoic Acid". Organic Syntheses. 60: 11. doi:10.15227/orgsyn.060.0011.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 12 April 2023, at 00:00
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy