Sulfadiazine

• Formula: C₁₀H₁₀N₄O₂S
• Molecular weight: 250.277
• IUPAC Standard InChI: InChI=1S/C10H10N4O2S/c11-8-2-4-9(5-3-8)17(15,16)14-10-12-6-1-7-13-10/h1-7H,11H2,(H,12,13,14) Copy

  
• IUPAC Standard InChIKey: SEEPANYCNGTZFQ-UHFFFAOYSA-N Copy
• CAS Registry Number: 68-35-9
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Benzenesulfonamide, 4-amino-N-2-pyrimidinyl-; Sulfanilamide, N1-2-pyrimidinyl-; A-306; Adiazin; Adiazine; Coco-Diazine; Cremodiazine; Debenal; Deltazina; Di-Azo-Mul; Diazin; Diazolone; Diazyl; Eskadiazine; Honey diazine; Lipo-Diazine; Lipo-Levazine; Liquadiazine; Microsulfon; N(Sup1)-2-Pyrimidinylsulfanilamide; N(Sup1)-2-Pyrimidylsulfanilamide; Neazine; Piridisir; Pirimal; Pyrimal; RP 2616; S. N. 112; Sanodiazine; Spofadrizine; Sterazine; Sulfadiazin; Sulfapirimidin; Sulfapyrimidine; Sulfazin; Sulfazine; Sulphadiazine; SDA; Theradiazine; 2-Sulfanilamidopyrimidine; 2-Sulfanilylaminopyrimidine; Codiazine; Cremotres; Metha-Meridiazine; Neotrizine; Palatrize; Pecta-diazine, suspension; Pyrimidine, 2-sulfanilamido-; Quadetts; Quadramoid; Sulfadiazene; Sulfanilamidopyrimidine; Sulfapyrimidin; Sulfatryl; Sulfolex; Sulfonsol; Sulfose; Terfonyl; Thi-Di-Mer; Tri-Sulfameth; Trifonamide; Triple Sulfas; Trisem; Truozine; 2-Sulfapyrimidine; Silvadene; N1-2-Pyrimidylsulfanilamide; N1-2-Pyrimidinylsulfanilamide; Diazovit; 2-(4-Aminobenzenesulfonamido)pyrimidine; Sulfanilamide, N1-2(1H)-pyrimidinylidene-; Sulfadiazina Reig Jofre; 2-(4-Aminobenzenesulfonylamino)pyrimidine; 2-(p-Aminobenzenesulfonamido)pyrimidin; 4-[[(Pyrimidin-2-yl)amino]sulfonyl]aniline; Sulphadiazine E; 4-Amino-N-(2-pyrmidinyl)benzene sulfonamide (sulfadiazine)
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Normal alkane RI, non-polar column, temperature ramp

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Sunwoo and Eisen, 1971
Sunwoo, C.; Eisen, H., Solubility parameter of selected sulfonamides, J. Pharm Sci., 1971, 60, 2, 238, https://doi.org/10.1002/jps.2600600217 . [all data]

Kofler and Sitte, 1950
Kofler, L.; Sitte, H., Melting Point Determination of Substances with Melt with Decomposition, Monatsh. Chem., 1950, 81, 619. [all data]

Martínez, Ávila, et al., 2003
Martínez, Fleming; Ávila, Carolina M.; Gómez, Alfredo, Thermodynamic study of the solubility of some sulfonamides in cyclohexane, J. Braz. Chem. Soc., 2003, 14, 5, 803-808, https://doi.org/10.1590/S0103-50532003000500016 . [all data]

MartÍnez and GÓmez, 2002
MartÍnez, Fleming; GÓmez, Alfredo, Estimation of the Solubility of Sulfonamides in Aqueous Media from Partition Coefficients and Entropies of Fusion, Physics and Chemistry of Liquids, 2002, 40, 4, 411-420, https://doi.org/10.1080/0031910021000017735 . [all data]

Martin, Wu, et al., 1985
Martin, A.; Wu, P.L.; Velasquez, T., Extended hildebrand solubility approach: Sulfonamides in binary and ternary solvents, J. Pharm. Sci., 1985, 74, 3, 277-282, https://doi.org/10.1002/jps.2600740311 . [all data]

Sunwoo and Eisen, 1971, 2
Sunwoo, Chimin; Eisen, Henry, Solubility parameter of selected sulfonamides, J. Pharm. Sci., 1971, 60, 2, 238-244, https://doi.org/10.1002/jps.2600600217 . [all data]

Roder and Stuthe, 1974
Roder, E.; Stuthe, W., Gas-chromatographisce Bestimmung von Sulfonamiden und ihren N4-Acetyl-Metaboliten aus Blut and Harn, Z. Anal. Chem., 1974, 271, 4, 281-283, https://doi.org/10.1007/BF00432831 . [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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