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Sigma-Aldrich 179418 Toluene ACS reagent, ≥99.5% CAS NO.: 108-88-3 2.5 L
Category
Brand
Stock Code
LB.SA.179418-2.5
Kısa Bilgi
Linear Formula: C6H5CH3 CAS Number: 108-88-3 Molecular Weight: 92.14 Beilstein: 635760 EC Number: 203-625-9 MDL number: MFCD00008512 UNSPSC Code: 12352005 eCl@ss: 39011102 PubChem Substance ID: 329751592 NACRES: NA.21
Market Price
KURUMSAL SATIŞ
| Sigma-Aldrich 179418 Toluene ACS reagent, ≥99.5% CAS NO.: 108-88-3 2.5 L |
| Linear Formula: C6H5CH3 CAS Number: 108-88-3 Molecular Weight: 92.14 Beilstein: 635760 EC Number: 203-625-9 MDL number: MFCD00008512 UNSPSC Code: 12352005 eCl@ss: 39011102 PubChem Substance ID: 329751592 NACRES: NA.21 |
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PROPERTIES
grade ACS reagent
Quality Level 200 Agency suitable for EPA 1613 vapor density 3.2 (vs air) vapor pressure 22 mmHg ( 20 °C) 26 mmHg ( 25 °C) Assay ≥99.5% form liquid autoignition temp. 997 °F expl. lim. 7 % dilution (for analytical testing) impurities H2SO4, passes test (darkened) ≤0.003% S compounds ≤0.030% water evapn. residue ≤0.0010% color APHA: ≤10 refractive index n/D 1.496 (lit.) bp 110-111 °C (lit.) mp -93 °C (lit.) density 0.865 g/mL at 25 °C (lit.) application(s) microbiology SMILES string Cc1ccccc1 InChI 1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3 InChI key YXFVVABEGXRONW-UHFFFAOYSA-N DESCRIPTION General description 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.[1] It has been reported to be a biotoxic solvent (toxic to many microorganisms at 0.1%v/v concentrations).[2] Its anaerobic biodegradation to CO2, by the denitrifying bacterium Thauera arornatica has been reported.[3] It forms a syndiotactic polystyrene-toluene molecular compound. Crystal structure of this molecular compound has been investigated by X-ray diffraction studies.[4] 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.[5] It may be used in the preparation of amine-capped gold nanocrystals.[6] Toluene undergoes alkylation in the presence of modified ZSM (Zeolite Socony Mobil)-5-class zeolite catalysts to form p-xylene with high selectivity.[7] When doped on graphene, it acts as an electron donor leading to alteration in graphene electrical properties.[8] |
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