Skip to Content
Merck
All Photos(2)

Key Documents

C121452

Sigma-Aldrich

p-Cymene

99%

Synonym(s):

1-Isopropyl-4-methylbenzene, 4-Isopropyltoluene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3C6H4CH(CH3)2
CAS Number:
Molecular Weight:
134.22
Beilstein:
1903377
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.62 (vs air)

Quality Level

vapor pressure

1.5 mmHg ( 20 °C)
3.7 mmHg ( 37.7 °C)

Assay

99%

form

liquid

autoignition temp.

817 °F

expl. lim.

5.6 %

refractive index

n20/D 1.490 (lit.)

bp

176-178 °C (lit.)

density

0.86 g/mL at 25 °C (lit.)

SMILES string

CC(C)c1ccc(C)cc1

InChI

1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3

InChI key

HFPZCAJZSCWRBC-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

p-Cymene is an alkyl aromatic hydrocarbon mainly used to study oxidation reactions under various conditions to synthesize highly valuable intermediates and building-blocks such as cymene hydroperoxide, 4-methyl acetophenone, 4-isopropyl benzyl alcohol, 4-isopropyl benzaldehyde and 4-isopropyl benzoic acid etc.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Inhalation - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3 - Repr. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Liquid-phase oxidation of p-cymene: Nature of intermediate hydroperoxides and relative activity of the alkyl groups
Serif, George Samuel and Hunt, CF and Bourns, AN
Canadian Journal of Chemistry, 31(12), 1229-1238 (1953)
Betelehem Wondwosen et al.
Malaria journal, 16(1), 39-39 (2017-01-25)
Maize cultivation contributes to the prevalence of malaria mosquitoes and exacerbates malaria transmission in sub-Saharan Africa. The pollen from maize serves as an important larval food source for Anopheles mosquitoes, and females that are able to detect breeding sites where
Electron-transfer processes: oxidation of naphthalene and p-cymene by peroxydisulfate
Giordano, Claudio and Belli, Aldo and Citterio, Attilio and Minisci, Francesco
The Journal of Organic Chemistry, 44(13), 2314-2315 (1979)
Loris Pinto et al.
Molecules (Basel, Switzerland), 25(20) (2020-10-22)
The aim of this work was to evaluate the antifungal activity in vapor phase of thymol, p-cymene, and γ-terpinene, the red thyme essential oil compounds (RTOCs). The Minimum Inhibitory Concentration (MIC) of RTOCs was determined against postharvest spoilage fungi of
Wei Zhou et al.
Journal of agricultural and food chemistry, 67(30), 8382-8392 (2019-07-05)
Staphylococcus aureus is a common pathogen that can cause life-threatening infections. Treatment of antibiotic-resistant S. aureus infection needs effective antibacterial agents. Thymol, a generally recognized safe natural compound, has potential as an alternative to treat S. aureus infections. However, the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service