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179418

Sigma-Aldrich

Toluène

ACS reagent, ≥99.5%

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About This Item

Formule linéaire :
C6H5CH3
Numéro CAS:
Poids moléculaire :
92.14
Numéro Beilstein :
635760
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352005
eCl@ss :
39011102
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

ACS reagent

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)

Pureté

≥99.5%

Forme

liquid

Température d'inflammation spontanée

997 °F

Limite d'explosivité

7 %

Impuretés

H2SO4, passes test (darkened)
≤0.003% S compounds
≤0.030% water

Résidus d'évap.

≤0.0010%

Couleur

APHA: ≤10

Indice de réfraction

n/D 1.496 (lit.)

Point d'ébullition

110-111 °C (lit.)

Pf

-93 °C (lit.)

Densité

0.865 g/mL at 25 °C (lit.)

Application(s)

microbiology

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 flammable liquid with a pungent odor, is widely employed as organic solvent. It is widely used as a precursor for synthesizing benzene and as a solvent in the paint industry. 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 has been employed as an solvent for the asymmetric synthesis of propargylic alcohols via addition reaction of terminal alkynes with various aldehydes in the presence of an optically active reagent, N-methylephedrine. It may be used in the preparation of amine-capped gold nanocrystals. Toluene undergoes alkylation in the presence of modified ZSM (Zeolite Socony Mobil)-5-class zeolite catalysts to form p-xylene with high selectivity. When doped on graphene, it acts as an electron donor leading to alteration in graphene electrical properties.

Conditionnement

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


Certificats d'analyse (COA)

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Les clients ont également consulté

Slide 1 of 4

1 of 4

Facile enantioselective synthesis of propargylic alcohols by direct addition of terminal alkynes to aldehydes.
Frantz DE, et al.
Journal of the American Chemical Society, 122(8), 1806-1807 (2000)
Synthesis and characterization of hydrophobic, organically-soluble gold nanocrystals functionalized with primary amines.
Leff DV, et al.
Langmuir, 12(20), 4723-4730 (1996)
Toluene.
von Burg R.
Journal of Applied Toxicology, 13(6), 441-446 (1993)
Selective alkylation of toluene with methanol to produce para-xylene.
Kaeding WW, et al.
J. Catal., 67(1), 159-174 (1981)
Electrochemical doping of graphene with toluene.
Kaverzin AA, et al.
Carbon, 49(12), 3829-3834 (2011)

Contenu apparenté

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

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