Sulfaguanidine

CAS Number57-67-0
Molecular FormulaC7H10N4O2S
Molecular Weight214.25
InChI KeyBRBKOPJOKNSWSG-UHFFFAOYSA-N
LogP-0.7
Synonyms
  • sulfaguanidine
  • 57-67-0
  • Sulfaguanidin
  • Sulphaguanidine
  • Sulfaguine
  • Guanicil
  • Sulfanilguanidine
  • Sulfoguanidine
  • Sulfaguanil
  • Sulfanilylguanidine
  • Sulfoguanil
  • Sulfoguanyl
  • Abiguanil
  • Guanidan
  • Sulfentidine
  • Aterian
  • Guamide
  • Orgaguanidon
  • Sulfaguanidinum
  • Sulfoguenil
  • Sulfoquanidine
  • Ganidan
  • N1-Amidinosulfanilamide
  • Resulfon
  • Suganyl
  • Diacta
  • Ruocid
  • Sulgin
  • N-Guanylsulfanilamide
  • S-Guanidine
  • 1-Sulfanilylguanidine
  • Sulfaguanidina
  • Shigatox
  • Guanidine, sulfanilyl-
  • p-Aminobenzenesulfonylguanidine
  • p-Aminobenzenesulfoguanidide
  • Sulginum
  • RP 2275
  • 2-(4-aminophenyl)sulfonylguanidine
  • Benzenesulfonamide, 4-amino-N-(aminoiminomethyl)-
  • Sulfanilamide, n(sup1)-amidino-
  • 4-Amino-N-(aminoiminomethyl)benzenesulfonamide
  • ((p-Aminophenyl)sulfonyl)guanidine
  • ((4-Aminophenyl)sulfonyl)guanidine
  • 1-((p-Aminophenyl)sulfonyl)guanidine
  • Solfaguanidina [DCIT]
  • Sulfaguamidine
  • 4-Amino-N-(diaminomethylene)benzenesulfonamide
  • A-307
  • Sulfanilamide, N1-amidino-
  • N-p-Aminobenzenesulphonylguanidine monohydrate
  • Sulfaguanidinum [INN-Latin]
  • N(sup 1)-Guanylsulfanilamide
  • Sulfaguanidina [INN-Spanish]
  • 4-Aminobenzenesulfonylguanidine
  • UNII-15XQ8043FN
  • N(sup 1)-Amidinosulfanilamide
  • 4-amino-N-[amino(imino)methyl]benzenesulfonamide
  • C7H10N4O2S
  • 4-amino-N-carbamimidoylbenzenesulfonamide
  • Emerin (pharmaceutical) (VAN)
  • Sulfaguanidine [INN]
  • Emerin (pharmaceutical)
  • EINECS 200-345-9
  • NSC 14041
  • Benzenesulfonamide, 4-amino-N-(diaminomethylene)-
  • N(sup 1)-(Diaminomethylene)sulfanilamide
  • AI3-01048
  • CHEMBL338802
  • BRBKOPJOKNSWSG-UHFFFAOYSA-N
  • 15XQ8043FN
  • 1-(4-aminophenyl)sulfonylguanidine
  • Sulfanilamide, N(sup 1)-amidino-
  • 2-(4-aminobenzenesulfonyl)guanidine
  • N-(4-aminobenzenesulfonyl)guanidine
  • Sulfaguanidine (INN)
  • Sulfaguanidine, 98%
  • CAS-57-67-0
  • NCGC00016252-01
  • Solfaguanidina
  • amino[(4-aminophenyl)sulfonyl]carboxamidine
  • 4-Amino-N-carbamimidoylbenzene-1-sulfonamide
  • 4-Amino-N-diaminomethylene-benzenesulfonamide
  • DSSTox_CID_3609
  • 4-amino-N-(diaminomethylidene)benzenesulfonamide
  • DSSTox_RID_77107
  • DSSTox_GSID_23609
  • [(p-Aminophenyl)sulfonyl]guanidine
  • [(4-Aminophenyl)sulfonyl]guanidine
  • 1-[(p-Aminophenyl)sulfonyl]guanidin

Applications:

HPLC Separation of Antibiotics on Newcrom A Column

June 11, 2020


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Antibiotics are widely used for treatment and prevention of bacterial infections.  Various antibiotics, particularly those with a sulfanilamide structure, were separated in HPLC using mixed-mode columns with varying strengths of ion-pairing groups.  Methanol can be used in the mobile phase on Newcrom A column.  The antibiotics were resolved on both columns with a gradient mobile phase consisting of acetonitrile (ACN) or methanol (MeOH), water and sulfuric acid (H2SO4) buffer.  UV detection at 275nm.

Condition
Column Newcrom A, 3.2 x 100 mm, 5 µm, 100 A
Mobile Phase MeOH Gradient
Buffer H2SO4 Gradient
Flow Rate  0.5 ml/min
Detection UV 275 nm

 

Description
Class of Compounds Drugs, Antibiotics
Analyzing Compounds Sulfanilamide, Sulfadiazine, Sulfaguanidine, Dapsone, Sulfaquinoxaline

Application Column

Newcrom A

Column Diameter: 3.2 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Dapsone
Sulfadiazine
Sulfaguanidine
Sulfanilamide
Sulphaquinoxaline
Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Antibiotics on Primesep 200 Column

June 6, 2020


HPLC.cloud
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Antibiotics are widely used for treatment and prevention of bacterial infections.  Various antibiotics, particularly those with a sulfanilamide structure, were separated in HPLC using mixed-mode columns with varying strengths of ion-pairing groups.  Primesep 200 has weak acidic ion-exchange pairing groups while Newcrom A has strong acidic ion-exchange groups.  In addition, methanol can be used in the mobile phase on Newcrom A column.  The antibiotics were resolved on both columns with a gradient mobile phase consisting of acetonitrile (ACN) or methanol (MeOH), water and sulfuric acid (H2SO4) buffer.  UV detection at 275nm.

Condition
Column Primesep 200, 4.6 x 100 mm, 5 µm, 100 A
Mobile Phase MeCN Gradient
Buffer H2SO4 – 0.5%
Flow Rate 1.0 ml/min
Detection UV 275 nm

 

Description
Class of Compounds Drugs, Antibiotics
Analyzing Compounds Sulfanilamide, Sulfadiazine, Sulfaguanidine, Dapsone, Sulfaquinoxaline

Application Column

Primesep 200

Column Diameter: 4.6 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

Add to cart
Application Analytes:
Dapsone
Sulfadiazine
Sulfaguanidine
Sulfanilamide
Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.