135070
Acide benzènesulfonique
technical grade, 90%
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About This Item
Formule linéaire :
C6H5SO3H
Numéro CAS:
Poids moléculaire :
158.18
Beilstein:
742513
Numéro MDL:
Code UNSPSC :
12352106
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Forme:
solid
Essai:
90%
Produits recommandés
Qualité
technical grade
Niveau de qualité
Essai
90%
Forme
solid
Groupe fonctionnel
sulfonic acid
Chaîne SMILES
OS(=O)(=O)c1ccccc1
InChI
1S/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9)
Clé InChI
SRSXLGNVWSONIS-UHFFFAOYSA-N
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Description générale
Benzenesulfonic acid, also known as besylic acid, is a strong organic acid commonly used as an acid catalyst in various organic reactions, such as esterification, alkylation, and condensation reactions. It is also used as a sulfonating agent to introduce sulfonic acid (SO3H) groups into organic compounds, which can be useful in the synthesis of several dye intermediates.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Code de la classe de stockage
8A - Combustible corrosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
N V V S S Raman et al.
Journal of pharmaceutical and biomedical analysis, 48(1), 227-230 (2008-07-08)
The present paper describes a simple isocratic reverse phase HPLC method for the determination of four genotoxic alkyl benzenesulfonates (ABSs) viz. methyl, ethyl, n-propyl and isopropyl benzenesulfonates (MBS, EBS, NPBS and IPBS) in amlodipine besylate (ADB). Good resolution between benzene
Chenghui Han et al.
Journal of hazardous materials, 168(1), 215-219 (2009-04-04)
A series of TiO(2)-Cu(2)O mixed oxides were prepared by the hydrolysis of titanium butoxide and reduction of copper acetate with hydrazine. These composite oxides were characterized by X-ray diffraction (XRD), inductively coupled plasma spectrometry (ICP), high-resolution transmission electron microscopy (HRTEM)
Wen Huang et al.
The Journal of organic chemistry, 73(17), 6845-6848 (2008-08-07)
A novel, convenient, and efficient method has been developed for selective synthesis of spirocycle, polycycle, and di- and tetrahydronaphthalene systems from aryl-substituted propargylic alcohols by FeCl3- or TsOH-catalyzed multiple activations of unsaturated C-C bonds and C-H bonds.
Snehlata Yadav et al.
European journal of medicinal chemistry, 45(12), 5985-5997 (2010-10-26)
A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones.
Ramasubbu Ramani et al.
Biomacromolecules, 9(5), 1390-1397 (2008-04-19)
We present lamellar self-assembly of cationic poly(L-histidine) (PLH) stoichiometrically complexed with an anionic surfactant, dodecyl benzenesulfonic acid (DBSA), which allows a stabilized conformation reminiscent of polyproline type II (PPII) left-handed helices. Such a conformation has no intrapeptide hydrogen bonds, and
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