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C121452

Sigma-Aldrich

p-Cymene

99%

Sinónimos:

1-Isopropyl-4-methylbenzene, 4-Isopropyltoluene

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About This Item

Fórmula lineal:
CH3C6H4CH(CH3)2
Número de CAS:
99-87-6
Peso molecular:
134.22
Beilstein/REAXYS Number:
1903377
EC Number:
202-796-7
MDL number:
MFCD00008893
UNSPSC Code:
12352100
PubChem Substance ID:
24892383
NACRES:
NA.22

vapor density

4.62 (vs air)

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

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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.

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

223190

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m-Cymene analytical standard

Supelco

30037

m-Cymene

α-Terpinene 85%

Sigma-Aldrich

223182

α-Terpinene

γ-Terpinene ≥95.0% (GC)

Sigma-Aldrich

86478

γ-Terpinene

Carvacrol 98%

Sigma-Aldrich

282197

Carvacrol

α-Terpinene ≥95.0% (GC)

Sigma-Aldrich

86473

α-Terpinene

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
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
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)
Carina Dettenrieder et al.
Sensors (Basel, Switzerland), 19(17) (2019-08-24)
A portable sensor system for the simultaneous detection of multiple environmentally relevant volatile organic compounds (VOCs) in real seawater based on Fourier transform infrared fiber-optic evanescent wave spectroscopy (FT-IR-FEWS) was developed. A cylindrical silver halide (AgX) fiber with an ethylene/propylene
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