MedKoo Cat#: 464192 | Name: Sulfadiazine-d4
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Sulfadiazine-d4 is intended for use as an internal standard for the quantification of sulfadiazine by GC- or LC-MS. Sulfadiazine is a sulfonamide antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria. It inhibits dihydropteroate synthase (DHPS), which converts a pteridine and 4-aminobenzoic acid (PABA) to dihydropteroate, an intermediate in folate biosynthesis. Sulfadiazine inhibits recombinant P. carinii DHPS (IC50 = 0.19 μM). It is active against clinical isolates of M. tuberculosis (MIC90 = 10 mg/L) and of N. meningitidis (MICs = 5-2,000 mg/L). Sulfadiazine is also active against A. pleuropneumoniae, S. choleraesuis, S. typhimurium, P. multocida, S. equi, and S. suis (MIC90s = <0.5 mg/ml for all) when used in combination with trimethoprim. In vivo, sulfadiazine (40 mg/kg per day) increases survival in a mouse model of lethal T. gondii infection when administered in combination with pyrimethamine. Formulations containing sulfadiazine have been used in the treatment of rheumatic fever and various infections, and, in a dual treatment with pyrimethamine, to treat toxoplasmosis.

Chemical Structure

Sulfadiazine-d4
Sulfadiazine-d4
CAS#1020719-78-1

Theoretical Analysis

MedKoo Cat#: 464192

Name: Sulfadiazine-d4

CAS#: 1020719-78-1

Chemical Formula: C10H6D4N4O2S

Exact Mass: 254.0776

Molecular Weight: 254.30

Elemental Analysis: C, 47.23; H, 5.55; N, 22.03; O, 12.58; S, 12.61

Price and Availability

Size Price Availability Quantity
1mg USD 600.00 2 Weeks
5mg USD 1,625.00 2 Weeks
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Synonym
Sulfadiazine-d4; Sulfadiazine d4;
IUPAC/Chemical Name
4-amino-N-(pyrimidin-2-yl)benzene-2,3,5,6-d4-sulfonamide
InChi Key
SEEPANYCNGTZFQ-QFFDRWTDSA-N
InChi Code
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)/i2D,3D,4D,5D
SMILES Code
O=S(NC1=NC=CC=N1)(C2=C(C([2H])=C(N)C([2H])=C2[2H])[2H])=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
to be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Solvent mg/mL mM
Solubility
To be determined 0.0 100.00
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 254.30 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
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Preparation of Electrospun Small Intestinal Submucosa/Poly(caprolactone-co-Lactide-co-glycolide) Nanofiber Sheet as a Potential Drug Carrier. Pharmaceutics. 2021 Feb 11;13(2):253. doi: 10.3390/pharmaceutics13020253. PMID: 33670418; PMCID: PMC7917610. 4: Ardabili S, Kohl J, Gül G, Hodel M. What obstetricians should be aware of: serious side effects of antibiotic toxoplasmosis treatment in pregnancy. BMJ Case Rep. 2021 Mar 1;14(3):e240809. doi: 10.1136/bcr-2020-240809. PMID: 33649030. 5: Nikahval B, Oryan A, Memarian P, Kamali A. Use of ovine acellular peritoneal matrix combined with honey and ovine fetal skin extract in the healing of full- thickness infected burn wounds in a rat model. Vet Res Forum. 2020 Fall;11(4):355-363. doi: 10.30466/vrf.2018.92422.2235. Epub 2020 Dec 15. PMID: 33643588; PMCID: PMC7904127. 6: Neves ACO, Viana AD, Menezes FG, Wanderlei Neto AO, Melo MCN, Gasparotto LHS. Biospectroscopy and chemometrics as an analytical tool for comparing the antibacterial mechanism of silver nanoparticles with popular antibiotics against Escherichia coli. Spectrochim Acta A Mol Biomol Spectrosc. 2021 Feb 6;253:119558. doi: 10.1016/j.saa.2021.119558. Epub ahead of print. PMID: 33631629. 7: Trachsel DS, Calloe K, J Rgensen E, Lunddahl CS, Pedersen PJ, Kanters JRK, Klaerke DA, Buhl R. Evaluation of electrocardiographic repolarization parameters after administration of trimethoprim-sulfadiazine, detomidine, or their combination in horses. Am J Vet Res. 2021 Mar;82(3):207-217. doi: 10.2460/ajvr.82.3.207. PMID: 33629897. 8: Jiang Y, Zhang Q, Deng X, Nan Z, Liang X, Wen H, Huang K, Wu Y. Single and competitive sorption of sulfadiazine and chlortetracycline on loess soil from Northwest China☆. Environ Pollut. 2020 Aug;263(Pt A):114650. doi: 10.1016/j.envpol.2020.114650. Epub 2020 Apr 27. PMID: 33618482. 9: da Silva GLP, Morais LCA, Olivato JB, Marini J, Ferrari PC. Antimicrobial dressing of silver sulfadiazine-loaded halloysite/cassava starch-based (bio)nanocomposites. J Biomater Appl. 2021 Feb 20:885328221995920. doi: 10.1177/0885328221995920. Epub ahead of print. PMID: 33611961. 10: Wang Y, Wang X, Zhou A, Li J, Tian L, Zhang M, Sun W, Ding L. A modified membrane filtration-ultraviolet photocatalytic system for the removal of trace sulfadiazine in drinking water (No. CHEM77354R1). Chemosphere. 2021 Feb 9;272:129867. doi: 10.1016/j.chemosphere.2021.129867. Epub ahead of print. PMID: 33601211. 11: Khattak S, Qin XT, Wahid F, Huang LH, Xie YY, Jia SR, Zhong C. Permeation of Silver Sulfadiazine Into TEMPO-Oxidized Bacterial Cellulose as an Antibacterial Agent. Front Bioeng Biotechnol. 2021 Jan 28;8:616467. doi: 10.3389/fbioe.2020.616467. PMID: 33585416; PMCID: PMC7876255. 12: Wang Z, Jia H, Liu Z, Peng Z, Dai Y, Zhang C, Guo X, Wang T, Zhu L. Greatly enhanced oxidative activity of δ-MnO2 to degrade organic pollutants driven by dominantly exposed {-111} facets. J Hazard Mater. 2021 Feb 2;413:125285. doi: 10.1016/j.jhazmat.2021.125285. Epub ahead of print. PMID: 33581670. 13: Zhang X, Chu Y, Zhang H, Hu J, Wu F, Wu X, Shen G, Yang Y, Wang B, Wang X. A mechanistic study on removal efficiency of four antibiotics by animal and plant origin precursors-derived biochars. Sci Total Environ. 2021 Jan 30;772:145468. doi: 10.1016/j.scitotenv.2021.145468. Epub ahead of print. PMID: 33581539. 14: Martínez-Pachón D, Echeverry-Gallego RA, Serna-Galvis EA, Villarreal JM, Botero-Coy AM, Hernández F, Torres-Palma RA, Moncayo-Lasso A. Treatment of wastewater effluents from Bogotá - Colombia by the photo-electro-Fenton process: Elimination of bacteria and pharmaceutical. Sci Total Environ. 2021 Jan 29;772:144890. doi: 10.1016/j.scitotenv.2020.144890. Epub ahead of print. PMID: 33578165. 15: Oaks RJ, Cindass R. Silver Sulfadiazine. 2021 Feb 13. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–. PMID: 32310514. 16: El-Hadidya SA, Abu-Melhab S. Some Studies in Sulfadiazine Incorporating Pyridine, Pyrimidine, Oxadiazole, and Azo Moieties Endowed with Pharmaceutical Potency. Acta Chim Slov. 2020 Mar;67(1):167-178. PMID: 33558911. 17: Costa IN, Ribeiro M, Silva Franco P, da Silva RJ, de Araújo TE, Milián ICB, Luz LC, Guirelli PM, Nakazato G, Mineo JR, Mineo TWP, Barbosa BF, Ferro EAV. Biogenic Silver Nanoparticles Can Control Toxoplasma gondii Infection in Both Human Trophoblast Cells and Villous Explants. Front Microbiol. 2021 Jan 21;11:623947. doi: 10.3389/fmicb.2020.623947. PMID: 33552033; PMCID: PMC7858645. 18: Stryjska K, Korona-Glowniak I, Chęcińska L, Kusz J, Ochocki J. Synthesis, Spectroscopy, Single-Crystal Structure Analysis and Antibacterial Activity of Two Novel Complexes of Silver(I) with Miconazole Drug. Int J Mol Sci. 2021 Feb 3;22(4):1510. doi: 10.3390/ijms22041510. PMID: 33546211; PMCID: PMC7919260. 19: Zhu F, Pan J, Zou Q, Wu M, Wang H, Xu G. Electron beam irradiation of typical sulfonamide antibiotics in the aquatic environment: Kinetics, removal mechanisms, degradation products and toxicity assessment. Chemosphere. 2021 Jan 26;274:129713. doi: 10.1016/j.chemosphere.2021.129713. Epub ahead of print. PMID: 33545585. 20: Zhu H, Hu B, Yang F. Removal of Sulfadiazine by Polyamide Nanofiltration Membranes: Measurement, Modeling, and Mechanisms. Membranes (Basel). 2021 Feb 2;11(2):104. doi: 10.3390/membranes11020104. PMID: 33540550; PMCID: PMC7912794.