33626

Sulfanilamide

puriss. p.a., ≥98% (calc. to the dried substance)

• 동의어(들): p-Aminobenzenesulfonamide
• Linear Formula: H₂NC₆H₄SO₂NH₂
• CAS Number: 63-74-1
• Molecular Weight: 172.20
• Beilstein: 511852
• EC Number: 200-563-4
• MDL number: MFCD00007939
• UNSPSC 코드: 12352100
• eCl@ss: 39093202
• PubChem Substance ID: 57648871
• NACRES: NA.21

속성

• grade: puriss. p.a.
• Quality Level: 100
• 분석: ≥98% (calc. to the dried substance)
• 양식: solid
• 불순물: ≤0.002% heavy metals (as Pb)
• 무기 잔류물: ≤0.1% (as SO₄)
• 손실: ≤0.5% loss on drying, 105 °C
• 색상: white to faint beige
• mp: 163-166 °C; 164-166 °C (lit.)
• 음이온 미량물: chloride (Cl^-): ≤100 mg/kg; sulfate (SO₄^2-): ≤200 mg/kg
• 항생제 활성 스펙트럼: Gram-negative bacteria; Gram-positive bacteria
• 동작 모드: DNA synthesis | interferes; enzyme | inhibits
• SMILES string: Nc1ccc(cc1)S(N)(=O)=O
• InChI: 1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)
• InChI key: FDDDEECHVMSUSB-UHFFFAOYSA-N
• 유전자 정보: human ... CA1(759), CA2(760), CA5A(763), CA5B(11238), CA9(768) ; mouse ... Car13(71934), Car5a(12352)

설명

일반 설명

Chemical structure: sulfonamide

Sulfanilamide (p-Aminobenzenesulfonamide) is a para-amino substituted benzenesulfonamide. Its ortho-mono and diiodo derivatives have been synthesized.

애플리케이션

• Study of new azo-azomethine derivatives of sulfanilamide: synthesis, characterization, spectroscopic, antimicrobial, antioxidant and anticancer activity: This study explores new derivatives of sulfanilamide synthesized through diazonium salt reactions and coupling with 2-hydroxy-3-methoxybenzaldehyde, providing insights into their potential antimicrobial, antioxidant, and anticancer activities (HS Al-Atbi, IJ Al-Assadi, et al., 2020).

포장

33626-100G; 33626-6X100G

기타 정보

Keep container tightly closed in a dry and well-ventilated place.

안전성 정보

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 1
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable
• 개인 보호 장비: Eyeshields, Gloves, type N95 (US)