Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

4-Methylbenzaldehyde

From Wikipedia, the free encyclopedia
4-Methylbenzaldehyde
Names
Preferred IUPAC name
4-Methylbenzaldehyde
Other names
p-Tolualdehyde; p-Tolylaldehyde
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.002.952 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C8H8O/c1-7-2-4-8(6-9)5-3-7/h2-6H,1H3 checkY
    Key: FXLOVSHXALFLKQ-UHFFFAOYSA-N checkY
  • InChI=1/C8H8O/c1-7-2-4-8(6-9)5-3-7/h2-6H,1H3
    Key: FXLOVSHXALFLKQ-UHFFFAOYAK
  • CC1=CC=C(C=C1)C=O
  • O=Cc1ccc(C)cc1
Properties
C8H8O
Molar mass 120.14852
Appearance colorless liquid
Density 1.019 g/mL (25 °C)
Melting point −6.00 °C (21.20 °F; 267.15 K)
Boiling point 204 to 205 °C (399 to 401 °F; 477 to 478 K)
1.545 (20 °C)
Hazards
Safety data sheet (SDS)
Related compounds
Related compounds
Benzaldehyde
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkYX markN ?)

4-Methylbenzaldehyde is the aromatic aldehyde with the formula CH3C6H4CHO. It is a colorless liquid. Commercially available, it may be prepared from the Friedel-Crafts formylation of toluene with carbon monoxide and hydrogen chloride under Gattermann-Koch conditions.[1] 4-Methylbenzaldehyde has a cherry-like scent similar to benzaldehyde, and finds some use in the fragrance industry.

4-Methylbenzaldehyde is a precursor to terephthalic acid, which is used to make various plastics.[2]

References

[edit]
  1. Coleman, G. H.; Craig, David (1932). "p-Tolualdehyde". Org. Synth. 12: 80. doi:10.15227/orgsyn.012.0080; Coll. Vol., vol. 2, 1943, p. 583.
  2. Brühne, Friedrich; Wright, Elaine (2011). "Benzaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_463.pub2. ISBN 978-3-527-30385-4.