Toluene

Name: Toluene
Brand: SIGALD

HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%

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About This Item

Linear Formula:

C₆H₅CH₃

CAS Number:

108-88-3

Molecular Weight:

92.14

NACRES:

NA.06

PubChem Substance ID:

329760030

eCl@ss:

39011102

UNSPSC Code:

12190000

EC Number:

203-625-9

MDL number:

MFCD00008512

Beilstein/REAXYS Number:

635760

grade:

HPLC Plus

assay:

≥99.9%

technique(s):

HPLC: suitable
gas chromatography (GC): suitable

application(s):

food and beverages

bp:

110-111 °C (lit.)
110.6 °C

vapor pressure:

22 mmHg ( 20 °C)
26 mmHg ( 25 °C)

Product Name

Toluene, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%

InChI key

YXFVVABEGXRONW-UHFFFAOYSA-N

InChI

1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3

SMILES string

Cc1ccccc1

grade

HPLC Plus

agency

suitable for EPA 1613

vapor density

3.2 (vs air)

vapor pressure

22 mmHg ( 20 °C)
26 mmHg ( 25 °C)

assay

≥99.9%

form

liquid

autoignition temp.

997 °F

expl. lim.

7 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.02% water

evapn. residue

≤0.0001%

halogenated residue

<10 ng/L (as heptachlor epoxide)

refractive index

n/D 1.496 (lit.)

bp

110-111 °C (lit.)
110.6 °C

mp

-93 °C (lit.)

density

0.865 g/mL at 25 °C (lit.)

UV absorption

λ: 284 nm A_max: 1.00
λ: 300 nm A_max: 0.10
λ: 325 nm A_max: 0.02
λ: 350 nm A_max: 0.005
λ: 400 nm A_max: 0.005

suitability

suitable for residue analysis

application(s)

food and beverages

Quality Level

100

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Related Categories

Analytical Chromatography

Gas Chromatography (GC) Solvents

HPLC Solvents

Lab Chemicals

Solvents

Application

Suitable for HPLC, spectrophotometry, environmental testing

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Pesticide Residue Analysis (as Heptachlor Epoxide) <10 ng/L

Packaging

M-Bottle for Solvents
As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!

pictograms

GHS02,GHS08,GHS07

signalword

Danger

hcodes

H225,H304,H315,H336,H361d,H373,H412

pcodes

P202 - P210 - P273 - P301 + P310 - P303 + P361 + P353 - P331

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 Inhalation - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

39.9 °F - closed cup

flash_point_c

4.4 °C - closed cup

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Analysis of Malondialdehyde, Chlorophyll Proline, Soluble Sugar, and Glutathione Content in Arabidopsis seedling.

Zhang Z and Huang R.

Bio-protocol, 3(14) (2013)

Liquid chromatography-atmospheric pressure photoionization-mass spectrometry analysis of triacylglycerol lipids--effects of mobile phases on sensitivity.

Sheng-Suan Cai et al.

Journal of chromatography. A, 1173(1-2), 88-97 (2007-10-30)

In this work, we evaluate the performance of liquid chromatography-atmospheric pressure photoionization-mass spectrometry (LC-APPI-MS) for non-aqueous reversed phase analysis of six triacylglycerol model compounds using six binary mobile phases including MeOH/iPrOH, MeOH/CHCl(3), MeOH/CH(2)Cl(2), CH(3)CN/iPrOH, CH(3)CN/CHCl(3), and CH(3)CN/CH(2)Cl(2). All mobile phases

Evidence that anaerobic oxidation of toluene in the denitrifying bacterium Thauera aromatica is initiated by formation of benzylsuccinate from toluene and fumarate.

T Biegert et al.

European journal of biochemistry, 238(3), 661-668 (1996-06-15)

Toluene is degraded anoxically to CO2 by the denitrifying bacterium Thauera aromatica. Toluene first becomes oxidized to benzoyl-CoA by O2-independent reactions. Benzoyl-CoA is then reduced to non-aromatic products by benzoyl-CoA reductase. We set out to study the reactions employed for

Structural study on syndiotactic polystyrene: 2. Crystal structure of molecular compound with toluene.

Chatani Y, et al.

Polymer, 34(8), 1620-1620 (1993)

A Pseudomonas thrives in high concentrations of toluene.

Inoue A and Horikoshi K.

Nature, 338, 264-266 (1989)

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