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270709

Sigma-Aldrich

Benzene

suitable for HPLC, ≥99.9%

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About This Item

Empirical Formula (Hill Notation):
C6H6
CAS Number:
71-43-2
Molecular Weight:
78.11
Beilstein/REAXYS Number:
969212
EC Number:
200-753-7
MDL number:
MFCD00003009
UNSPSC Code:
12190000
PubChem Substance ID:
329752965
NACRES:
NA.21

vapor density

2.77 (vs air)

Quality Level

100

vapor pressure

166 mmHg ( 37.7 °C)
74.6 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

1043 °F

expl. lim.

8 %

technique(s)

HPLC: suitable

impurities

≤0.02% water (Karl Fischer)

evapn. residue

<0.0005%

color

APHA: ≤20

refractive index

n20/D 1.501 (lit.)

bp

80 °C (lit.)

mp

5.5 °C (lit.)

density

0.874 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 280 nm Amax: 1.0
λ: 290 nm Amax: 0.15
λ: 300 nm Amax: 0.06
λ: 330 nm Amax: 0.02
λ: 350-400 nm Amax: 0.01

application(s)

food and beverages

SMILES string

c1ccccc1

InChI

1S/C6H6/c1-2-4-6-5-3-1/h1-6H

InChI key

UHOVQNZJYSORNB-UHFFFAOYSA-N

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Biochem/physiol Actions

Environmental carcinogen; hematoxin that is linked to increased incidence of leukemia in humans.

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signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Carc. 1A - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 1B - Skin Irrit. 2 - STOT RE 1

target_organs

Blood

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

12.2 °F - closed cup

flash_point_c

-11.0 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Luoping Zhang et al.
Critical reviews in toxicology, 32(1), 1-42 (2002-02-16)
Benzene is an established cause of human leukemia that is thought to act by producing chromosomal aberrations and altered in cell differentiation. In several recent studies increased levels of chromosomal aberrations in peripheral blood lymphocytes were correlated with a heightened
Use of the CNDO method in spectroscopy. I. Benzene, pyridine, and the diazines.
Del Bene J and Jaffe HH.
J. Chem. Phys. , 48(44), 1807-1813 (1968)
Benzene forms hydrogen bonds with water.
Suzuki S, et al.
Science, 257(5072), 942-945 (1992)
M Kiguchi et al.
Physical review letters, 101(4), 046801-046801 (2008-09-04)
Highly conductive molecular junctions were formed by direct binding of benzene molecules between two Pt electrodes. Measurements of conductance, isotopic shift in inelastic spectroscopy, and shot noise compared with calculations provide indications for a stable molecular junction where the benzene
Filamentous growth of carbon through benzene decomposition.
Oberlin A, et al.
Journal of Crystal Growth, 32(3), 335-349 (1976)
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