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.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
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

3-Methyl-2-butanol

From Wikipedia, the free encyclopedia

3-Methyl-2-butanol[1]
Names
Preferred IUPAC name
3-Methylbutan-2-ol[2]
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.009.047 Edit this at Wikidata
EC Number
  • 209-950-2
UNII
UN number 1105
  • InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3 checkY
    Key: MXLMTQWGSQIYOW-UHFFFAOYSA-N checkY
  • CC(C)C(C)O
Properties
C5H12O
Molar mass 88.150 g·mol−1
Appearance Colorless liquid
Density 818 mg cm−3
Boiling point 109 to 115 °C; 228 to 239 °F; 382 to 388 K
59 g dm−3
Solubility in ethanol miscible
log P 1.036
Vapor pressure 1.20 kPa
Thermochemistry
245.9 J K−1 mol−1
-371.3--368.5 kJ mol−1
-3.3157--3.3145 MJ mol−1
Hazards
GHS labelling:
GHS02: Flammable
GHS07: Exclamation mark
Warning
H226, H332, H335
P261
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
3
0
Flash point 34 °C (93 °F; 307 K)
Related compounds
Related compounds
 Amyl alcohol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

3-Methyl-2-butanol (IUPAC name, commonly called sec-isoamyl alcohol) is an organic chemical compound. It is used as a solvent and an intermediate in the manufacture of other chemicals.[3]

YouTube Encyclopedic

  • 1/3
    Views:
    6 311
    7 880
    24 849
  • 361L Dehydration of 2-methyl-2-butanol (#9)
  • Alcohol Dehydration of 1-butanol & 2-butanol Using H2SO4 - E1 & E2 Mechanism
  • Alcohol Dehydration Reaction Mechanism With H2SO4 - Acid Catalyzed

Transcription

References

  1. ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–374, 5–42, 8–102, 15–22, ISBN 0-8493-0594-2
  2. ^ "sec-Isoamyl alcohol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Retrieved 13 October 2011.
  3. ^ The compound is one of the eight isomers of pentyl alcohol. McKetta, John J.; Cunningham, William Aaron (1977), Encyclopedia of Chemical Processing and Design, vol. 3, Boca Raton, Florida: CRC Press, pp. 280–281, ISBN 978-0-8247-2480-1, retrieved 17 January 2010

Stub icon

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

This page was last edited on 25 March 2022, at 01:18
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