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34866

Sigma-Aldrich

Toluène

suitable for HPLC, 99.9%

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About This Item

Formule linéaire :
C6H5CH3
Numéro CAS:
Poids moléculaire :
92.14
Beilstein:
635760
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116105
eCl@ss :
39011102
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

HPLC grade

Niveau de qualité

Agence

suitable for EPA 1613

Densité de vapeur

3.2 (vs air)

Pression de vapeur

22 mmHg ( 20 °C)
26 mmHg ( 25 °C)

Essai

99.9%

Forme

liquid

Température d'inflammation spontanée

997 °F

Limite d'explosivité

7 %

Technique(s)

HPLC: suitable
UV/Vis spectroscopy: suitable

Impuretés

≤0.0005% non-volatile matter
≤0.0005% thiophene
≤0.001% free acid (as HCl)
≤0.02% water (Karl Fischer)

Indice de réfraction

n/D 1.496 (lit.)

pb

110-111 °C (lit.)

Pf

-93 °C (lit.)

Densité

0.865 g/mL at 25 °C (lit.)

Absorption UV

λ: 286 nm Amax: ≤1.00
λ: 288 nm Amax: ≤0.50
λ: 293 nm Amax: ≤0.20
λ: 300 nm Amax: ≤0.10
λ: 310 nm Amax: ≤0.05
λ: 335 nm Amax: ≤0.02
λ: 350 nm Amax: ≤0.004

Application(s)

food and beverages

Chaîne SMILES 

Cc1ccccc1

InChI

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

Clé InChI

YXFVVABEGXRONW-UHFFFAOYSA-N

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Description générale

Toluene, a benzene analog, is widely employed as an organic solvent. It has been reported to be a biotoxic solvent (toxic to many microorganisms at 0.1%v/v concentrations). Its anaerobic biodegradation to CO2, by the denitrifying bacterium Thauera arornatica has been reported. It forms a syndiotactic polystyrene-toluene molecular compound. Crystal structure of this molecular compound has been investigated by X-ray diffraction studies.

Application

Toluene may be used as a doping agent during the quantitative estimation of triacylglycerols (TAGs) by liquid chromatography-atmospheric pressure photoionization-mass spectrometry (LC-APPIMS). It has been reported to improve the sensitivity of analysis. It may be used as solvent for the preparation of 4-arm polylactide-based (PLA) star oligomer.

Conditionnement

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!

Autres remarques

Important notice
  • The article number 34866-4X2.5L will be discontinued. Please order the single bottle 34866-2.5L which is physically identical with the same exact specifications.
  • The article number 34866-6X1L will be discontinued. Please order the single bottle 34866-1L which is physically identical with the same exact specifications.

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Pictogrammes

FlameHealth hazardExclamation mark

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

39.9 °F - closed cup

Point d'éclair (°C)

4.4 °C - closed cup


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Les clients ont également consulté

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Direct laser writing of 3D scaffolds for neural tissue engineering applications.
Melissinaki V, et al.
Biofabrication, 3(4), Direct laser writing-Direct laser writing (2011)
A Pseudomonas thrives in high concentrations of toluene.
Inoue A and Horikoshi K.
Nature, 338, 264-266 (1989)
Structural study on syndiotactic polystyrene: 2. Crystal structure of molecular compound with toluene.
Chatani Y, et al.
Polymer, 34(8), 1620-1620 (1993)
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
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

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