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
Languages
Recent
Show all languages
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

Isobutylbenzene

From Wikipedia, the free encyclopedia

Isobutylbenzene
Names
Preferred IUPAC name
(2-Methylpropyl)benzene
Other names
Isobutylbenzene
Identifiers
3D model (JSmol)
1852218
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.007.916 Edit this at Wikidata
EC Number
  • 208-706-2
261101
UNII
UN number 2709
  • InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3 checkY
    Key: KXUHSQYYJYAXGZ-UHFFFAOYSA-N checkY
  • InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3
  • CC(C)CC1=CC=CC=C1
Properties[1]
C10H14
Molar mass 134.222 g·mol−1
Appearance Colorless liquid
Odor Aromatic
Density 0.853 g/cm3, liquid
Melting point −51 °C (−60 °F; 222 K)
Boiling point 170 °C (338 °F; 443 K)
Vapor pressure 4.2 mmHg (37.7 °C)
1.486
Hazards[1]
GHS labelling:
GHS02: Flammable
GHS07: Exclamation mark
GHS08: Health hazard
Danger
H226, H304, H315, H319, H335, H336
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P301+P310, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P331, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth (blue): no hazard codeFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability (yellow): no hazard codeSpecial hazards (white): no code
2
Safety data sheet (SDS) ICSC 0113
Related compounds
Related compounds
 n-Butylbenzene, sec-Butylbenzene, tert-Butylbenzene, Cumene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Isobutylbenzene is a chemical compound with the molecular formula C10H14.[2] It is used in the industrial manufacture of ibuprofen.

Isobutylbenzene is a colorless flammable liquid that is a respiratory irritant.

Industrial production is through catalytic carbometalation: toluene adds to propene in the presence of a sodium-potassium catalyst on activated carbon.[3]

YouTube Encyclopedic

  • 1/5
    Views:
    623
    7 416
    457
    26 602
    341
  • CLEMMENSEN REDUCTION.#ncchem
  • naming iso, sec, & tert R-groups
  • The treatment of benzene with isobutene
  • SYNTHESIS OF IBUPROFEN | MEDICINAL CHEMISTRY | GPAT-2020 | B.PHARM-4TH SEM
  • polysub aromatics

Transcription

References

  1. ^ a b Isobutylbenzene, International Chemical Safety Card 0113, Geneva: International Programme on Chemical Safety, April 2005.
  2. ^ "Isobutylbenzene | C10H14 | ChemSpider". www.chemspider.com. Retrieved 2018-12-01.
  3. ^ U.S. Patent #2995610, "Isobutylbenzene Preparation". Assigned August 8, 1961 to Standard Oil Co.
Stub icon

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

This page was last edited on 25 February 2024, at 23:49
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