Skip to Content
Merck
CN

46762

Supelco

Sulfabenzamide

VETRANAL®, analytical standard

Synonym(s):

N-(4-Aminobenzenesulfonyl)benzamide, N-Sulfanilylbenzamide

Sign Into View Organizational & Contract Pricing

Select a Size

About This Item

Empirical Formula (Hill Notation):
C13H12N2O3S
CAS Number:
127-71-9
Molecular Weight:
276.31
Beilstein:
2139003
EC Number:
204-859-4
MDL number:
MFCD00044890
UNSPSC Code:
41116107
PubChem Substance ID:
329757239
NACRES:
NA.24

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

analytical standard

Quality Level

200

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

clinical testing

format

neat

SMILES string

Nc1ccc(cc1)S(=O)(=O)NC(=O)c2ccccc2

InChI

1S/C13H12N2O3S/c14-11-6-8-12(9-7-11)19(17,18)15-13(16)10-4-2-1-3-5-10/h1-9H,14H2,(H,15,16)

InChI key

PBCZLFBEBARBBI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Chemical structure: sulfonamide

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBW2565

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ahmad G Nozad et al.
Biophysical chemistry, 139(2-3), 116-122 (2008-11-26)
A systematic computational study was carried out to characterize the hydrogen bond, HB, interactions of sulfabenzamide crystal structure by DFT calculations of electric field gradient, EFG, tensors at the sites of 14N, 17O, and 2H nuclei. The computations were performed
[Physico-chemical comparison of two sulfamides: sulfaproxyline and sulfabenzamide].
L Maury et al.
Pharmaceutica acta Helvetiae, 62(4), 116-120 (1987-01-01)
B M Jones et al.
Antimicrobial agents and chemotherapy, 21(6), 870-872 (1982-06-01)
Recent reports suggest that anaerobic Bacteroides organisms are frequently found with Gardnerella vaginalis in nonspecific vaginitis. Specimens taken from 96 women with vaginal discharge were tested simultaneously for these organisms. G. vaginalis was found in 73% of the specimens, Bacteroides
Nino G Todua et al.
Rapid communications in mass spectrometry : RCM, 25(6), 750-754 (2011-02-22)
Mono-, di- and trialkyl derivatives of 'sulfabenzamide' (N-4-aminophenylsulfonylbenzamide) have been prepared and their electron ionization (EI) mass spectra examined. It is found that the fragmentation of N-alkylsulfabenzamides (alkyl = CH(3) to n-C(5)H(11)) proceeds via a very specific rearrangement process. The proposed mechanism
C A Spinks et al.
Bioconjugate chemistry, 10(4), 583-588 (1999-07-20)
Molecular modeling of hapten structure was used to predict and influence, through appropriate synthetic work, the outcome of an immunization program. Examination of the structures of sulfonamide antibiotics led to the development of a hypothesis and the consequent synthesis of
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service