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Chemical Name


Benzenesulfonamide, 4-amino- (C6H8N2O2S)

Compound Descriptions:

Structure Drawing
Formula:C6H8N2O2S
Molecular Weight:172.205 g/mol
Name(s):Benzenesulfonamide, 4-amino-
Sulfanilamide
p-Aminobenzolsulfonamid
p-Aminobenzol-sulfonsäureamid (α-Form)
p-Aminobenzol-sulfonsäureamid (β-Form)
p-Aminobenzol-sulfonsäureamid (γ-Form)
4-(Aminosulfonyl)aniline
4-Aminobenzenesulfonamide
4-Aminophenylsulfonamide
4-Sulfamoylaniline
A-349
Albexan
Albosal
Ambeside
Antistrept
Astreptine
Astrocid
Bacteramid
Bactesid
Collomide
Colsulanyde
Copticide
Deseptyl
Dipron
Ergaseptine
Erysipan
Estreptocida
Exoseptoplix
F 1162
Fourneau 1162
Gerison
Gombardol
Infepan
Lusil
Lysococcine
Neococcyl
Orgaseptine
p-Aminobenzenesulfonamide
p-Aminophenylsulfonamide
p-Anilinesulfonamide
p-Sulfamidoaniline
p-Sulfamoylaniline
PABS
Prontalbin
Prontosil Album
Prontosil I
Prontosil white
Prontylin
Pronzin Album
Proseptal
Proseptine
Proseptol
Pysococcine
Ro 1-3354
Rubiazol A
Sanamid
sulphanilamide
sulfanilamide (INN)
p-amino-benzolsulfonamide
4-amino-benzenesulfonamide
4-aminobenzenesulphonamide
p-Aminobenzenesulfamide
p-Aminobenzenesulfonylamide
Aniline-p-sulfonic amide
Benzenesulfonamide, p-amino-
Septamide Album
Septanilam
Septinal
Septolix
Septoplex
Stopton Album
Stramid
Strepamide
Strepsan
Streptagol
Streptamid
Streptamin
Streptasol
Streptocid album
Streptocide White
Streptoclase
Streptocom
Streptol
Strepton
Streptopan
Streptosil
Streptozol
Streptozone
Streptrocide
Sulfamidyl
Sulfamine
Sulfana
Sulfanalone
Sulfanidyl
Sulfanilimidic acid
Sulfocidine
Sulfonamide P
Therapol
Tolder
White streptocide
1162 F
4-Aminobenzolsulfonamid
Sulfanilsäureamid
Anilin-4-sulfonsäureamid
(4-(Aminosulfonyl)phenyl)amine
1162F
NSC 7618
Streptocide (white)
Sulfanilamide Vaginal Cream
p-Aminobenzol-sulfonsäureamid (a-Form)
p-Aminobenzol-sulfonsäureamid (ß-Form)
p-Aminobenzol-sulfonsäureamid (?-Form)
CAS-RN:63-74-1, 1337-36-6, 1337-39-9, 12765-80-9, 24706-25-0, 102489-34-9
EINECS:200-563-4 EINECS
Classification:no charge; carbocycle; aromatic; 6RingOnly; 6ring; 1fragment

European Regulations

1 matching entries in european regulations: ECHA-pre

Derivatives / Analogues

Derivativehydrate salt: Natrium-sulfanilamid-monohydrat 
Derivativehydrate: Sulfanilamid-monohydrat 

Landolt-Börnstein Citations:

Crystallography, Structure and Morphology

 Structure Data of Organic Crystals: Vol. III/5a 2:6-8-47, p.296III/5a

Magnetic Properties

 Diamagnetic Susceptibility: Vol. II/27b 7.1.6:665II/27B

Mechanical Properties

Spectroscopic Methods

 Nuclear Magnetic Resonance (NMR) Data - 13C: Vol. III/35d2 2.4, p.23III/35D2
 Nuclear quadrupole resonance data tables: Nitrogen: C6H4N2 - C6H11N: Vol. III/20a 3.2:7-66III/20a

References

II/27B
Short: II/27B
Title: Diamagnetic Susceptibility of Organic Compounds, Oils, Paraffins and Polyethylenes
Author: Kumar, M.; Gupta, R.
Editor: Gupta, Radha Raman
Source: Landolt-Börnstein, New Series
Volume: II/27B
Year: 2008
Keyword: diamagnetic susceptibility; organic compounds
ISBN: 978-3-540-44359-9 (print)
ISBN: 978-3-540-45860-9 (online)
Internet Resource: doi:10.1007/978-3-540-45860-9
RefComment: VIII, 503 p. With CD-ROM., Hardcover
RefComment: Written for: Scientists and researchers in the fields of physics, chemistry, materials science
RefComment: Supplement and Revised Editon to II/16
Abstract: The volume II/27 has been divided into three subvolumes according to the classes of compounds: Subvolume A: Diamagnetic susceptibility and magnetic anisotropy of inorganic and organometallic compounds; Subvolume B: Diamagnetic susceptibility of organic compounds, oils, paraffins and polyethylenes; Subvolume C: Diamagnetic susceptibility and magnetic anisotropy of organic compounds. The data presented in this volume are based on the literature survey of the chemical abstracts up to 2005. The calculated values of diamagnetic susceptibility of organic compounds in the present subvolume II/27B are presented along with their experimental values. They have been calculated with the use of structural parameters in structural formula by using different theoretical methods available in the literature.
III/20a
Short: III/20a
Title: Nuclear Quadrupole Resonance Spectroscopy Data: Nuclei D ... Cl
Author: Chihara, H.; Nakamura, N.
Editor: Hellwege, K.-H.; Hellwege, A.M.
Source: Landolt-Börnstein, New Series
Volume: III/20a
Year: 1988
Keyword: NQR
ISBN: 3-540-18161-X
ISBN: 978-3-540-18161-3
Internet Resource: DOI:10.1007/b31153
RefComment: IX,677 pages. Hardcover
Abstract: Nuclear Quadrupole Resonance Spectroscopy has become a standard method for structural research in molecular and solid state physics as well as for different branches of chemistry. The volumes cover data for more than 8,000 substances in the solid state. Data for free molecules have been published in volumes II/14 and II/15 of the New Series. The tables are arranged according to the atomic number of the elements.
III/35D2
Short: III/35D2
Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 2: Aromatic Compounds
Author: Mikhova, B.
Editor: Gupta, R.R.; Lechner, M.D.
Source: Landolt-Börnstein, New Series
Volume: III/35D2
Year: 2005
Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure
ISBN: 978-3-540-20189-2
ISBN: 3-540-20189-0
Internet Resource: DOI:10.1007/b83345
RefComment: VIII, 291 p., Hardcover
RefComment: Written for Science and engineers in the fields of physics, chemistry and physical chemistry who inted to use NMR to study the structure and the binding of molecules
Abstract: Nuclear Magnetic Resonance (NMR) is based on the fact that certain nuclei exhibit a magnetic moment, orient by a magnetic field, and absorb characteristic frequencies in the radiofrequency part of the spectrum. The spectral lines of the nuclei are highly influenced by the chemical environment i.e. the structure and interaction of the molecules. NMR is now the leading technique and a powerful tool for the investigation of the structure and interaction of molecules. The present Landolt-Börnstein volume III/35 Nuclear Magnetic Resonance (NMR) Data is therefore of major interest to all scientists and engineers who intend to use NMR to study the structure and the binding of molecules. Volume III/35 "NMR-Data" is divided into several subvolumes and parts. Subvolume III/35A contains the nuclei 11B and 31P, subvolume III/35B contains the nuclei 19F and 15N, subvolume III/35C contains the nucleus 1H, subvolume III/35D contains the nucleus 13C, subvolume III/35E contains the nucleus 17O, and subvolume III/35G contains the nucleus 77Se. More nuclei will be presented later.
III/5a
Short: III/5a
Title: Structure Data of Organic Crystals: C ... C 13
Author: Schudt, E.; Weitz, G.
Editor: Hellwege, K.-H.; Hellwege, A.M.
Source: Landolt-Börnstein, New Series
Volume: III/5a
Year: 1971
ISBN: 3-540-05177-5
ISBN: 978-3-540-05177-0
Internet Resource: DOI:10.1007/b19970
RefComment: XXI, 736 pages, and VII, 890 pages. Hardcover
Abstract: Volume III/5 offers a compitation as complete as possible of the space groups and lattice con-stants of all crystals which have been studied by means of X-rays, neutron and electron diffraction.
IV/1a
Short: IV/1a
Title: Densities of Liquid Systems: Nonaqueous Systems and Ternary Aqueous Systems
Author: Lacmann, R.; Synowietz, C.
Editor: Schäfer, Kl.
Source: Landolt-Börnstein, New Series
Volume: IV/1a
Year: 1974
ISBN: 3-540-06269-6
ISBN: 978-3-540-06269-1
Internet Resource: DOI:10.1007/b20003
RefComment: X, 716 pages. Hardcover
Abstract: Volume IV/1 contains information on the densities of liquid systems. It may be considered as a supplement to volume II/1 of the 6th Edition, which contains only a few data on nonaqueous systems. Data are not listed for all systems but primarily for those of greater interest where data for a larger range of concentrations were available.
EINECS
Short: EINECS
Title: EINECS (European Inventory of Existing Commercial Chemical Substances)
Source: Official Journal of the European Communities
Volume: C 146 A (15.06.1990)
Page: 1
Year: 1990
Publish_Date: 1990/06/15

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