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95682

Sigma-Aldrich

p-Xylene

puriss. p.a., ≥99.0% (GC)

Synonym(s):

1,4-Dimethylbenzene

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About This Item

Linear Formula:
C6H4(CH3)2
CAS Number:
Molecular Weight:
106.17
Beilstein/REAXYS Number:
1901563
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
assay:
≥99.0% (GC)
technique(s):
GC/GC: suitable
bp:
138 °C (lit.)
vapor pressure:
9 mmHg ( 20 °C)

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vapor density

3.7 (vs air)

Quality Level

vapor pressure

9 mmHg ( 20 °C)

grade

puriss. p.a.

assay

≥99.0% (GC)

form

liquid

autoignition temp.

984 °F

expl. lim.

7 %

technique(s)

GC/GC: suitable

impurities

≤0.5% o- and m-xylene (GC)
≤0.5% toluene (GC)

evapn. residue

≤0.002%

refractive index

n20/D 1.495 (lit.)
n20/D 1.495

bp

138 °C (lit.)

mp

12-13 °C (lit.)

solubility

water: soluble 0.2 g/L

density

0.861 g/mL at 20 °C (lit.)

cation traces

Al: ≤0.5 mg/kg
Ba: ≤0.1 mg/kg
Bi: ≤0.1 mg/kg
Ca: ≤0.5 mg/kg
Cd: ≤0.05 mg/kg
Co: ≤0.02 mg/kg
Cr: ≤0.02 mg/kg
Cu: ≤0.02 mg/kg
Fe: ≤0.1 mg/kg
K: ≤0.5 mg/kg
Li: ≤0.1 mg/kg
Mg: ≤0.1 mg/kg
Mn: ≤0.02 mg/kg
Mo: ≤0.1 mg/kg
Na: ≤0.5 mg/kg
Ni: ≤0.02 mg/kg
Pb: ≤0.1 mg/kg
Sr: ≤0.1 mg/kg
Zn: ≤0.1 mg/kg

SMILES string

Cc1ccc(C)cc1

InChI

1S/C8H10/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3

InChI key

URLKBWYHVLBVBO-UHFFFAOYSA-N

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General description

p-Xylene is an isomeric form of xylene. It undergoes Friedel-Crafts acylation reaction with various acids in the presence of zeolites (catalyst).[1] It can be obtained from the mixtures of isomeric forms of xylene and ethylbenzene, isolated from the naptha fraction of petroleum. Also, it can be prepared from toluene by employing ZSM (Zeolite Socony Mobil)-5 catalysts.[2] It is a raw material for the manufacture of PET (poly(ethylene terephthalate)) bottles.[3] Sustainable synthesis of xylene from ethylene and dimethylfuran in the presence of zeolite catalysts has been reported.[2][3]

Application

p-Xylene may be used in the synthesis of poly-p-xylene[4] and terephthalic acid.[5]

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Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

80.6 °F - closed cup

flash_point_c

27 °C - closed cup


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Friedel-Crafts acylation of toluene and p-xylene with carboxylic acids catalyzed by zeolites.
Chiche B, et al.
The Journal of Organic Chemistry, 51(11), 2128-2130 (1986)
Cycloaddition of biomass-derived furans for catalytic production of renewable p-xylene.
Williams CL, et al.
ACS Catalysis, 2(6), 935-939 (2012)
Ultra-selective cycloaddition of dimethylfuran for renewable p-xylene with H-BEA.
Chang CC, et al.
Green Chemistry, 16(2), 585-588 (2014)
Metal-organic framework MIL-101 for high-resolution gas-chromatographic separation of xylene isomers and ethylbenzene.
Zhi-Yuan Gu et al.
Angewandte Chemie (International ed. in English), 49(8), 1477-1480 (2010-01-22)
Yusuke Yamada et al.
Physical chemistry chemical physics : PCCP, 14(27), 9654-9659 (2012-06-14)
The catalytic durability of an organic photocatalyst, 9-mesityl-10-methyl acridinium ion (Acr(+)-Mes), has been dramatically improved by the addition of [{tris(2-pyridylmethyl)amine}Cu(II)](ClO(4))(2) ([(tmpa)Cu(II)](2+)) in the photocatalytic oxygenation of p-xylene by molecular oxygen in acetonitrile. Such an improvement is not observed by the

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