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sulfadimidine

Sulfamethazine Base

CAS: 57-68-1

Molecular Formula: C12H14N4O2S

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sulfadimidine - Names and Identifiers

Name Sulfamethazine Base
Synonyms SM2
A-502
Azolmetazin
SULFAMETAZINE
Sulfadimidine
Sulfamethazine
Sulphadimidine
Sulfamethazine Base
Sulfadimidine solution
sulfadimidine standard solution
N1-(4,6-Dimethyl-2-pyrimidinyl)sulfanilamide
6-(4'-Aminobenzol-sulfonamido)-2,4-dimethylpyrimidin
6-(4'-aminobenzol-sulfonamido)-2,4-dimethylpyrimidin
2-(4-Aminobenzenesulfonamido)-4,6-dimethylpyrimidine
(p-Aminobenzolsulfonyl)-2-amino-4,6-dimethylpyrimidin
benzenesulfonamide,4-amino-N-(4,6-dimethyl-2-pyrimiidinyl)-
Benzenesulfonamide, 4-amino-N-(4,6-dimethyl-2-pyrimidinyl)-
CAS 57-68-1
EINECS 200-346-4
InChI InChI=1/C12H14N4O2S/c1-8-7-9(2)15-12(14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16)

sulfadimidine - Physico-chemical Properties

Molecular FormulaC12H14N4O2S
Molar Mass278.33
Density1.2997 (rough estimate)
Melting Point197 °C
Boling Point294°C (rough estimate)
Water Solubility150mg/100mL (29 ºC)
Solubility Almost insoluble in water (solubility: 29°C,150mg/100ml;37°C,192 mg/ml), dissolved in hot ethanol, insoluble in ether, easily soluble in dilute acid or dilute alkali solution.
AppearanceWhite or yellowish crystals or powders
Colorwhite to off-white
Merck14,8905
BRN261304
pKa7.4, 2.65(at 25℃)
Storage Condition2-8°C
StabilityStable, but light sensitive. Incompatible with strong oxidizing agents.
SensitiveSensitive to light
Refractive Index1.6440 (estimate)
MDLMFCD00006066
Physical and Chemical PropertiesMelting point 197-200°C
water-soluble 150mg/100mL (29°C)
UseHas inhibitory effect on hemolytic Streptococcus, Pneumonia coccus and meningitis and other bacteria

sulfadimidine - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS23 - Do not breathe vapour.
S24/25 - Avoid contact with skin and eyes.
S36 - Wear suitable protective clothing.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany2
RTECSWO9275000
FLUKA BRAND F CODES10
TSCAYes
HS Code29350090
ToxicityLD50 i.p. in mice: 1.06 g/kg (Bobranski)

sulfadimidine - Upstream Downstream Industry

Raw MaterialsSodium carbonate
Cyclohexanone
Sulphaguanidine
2,4-Pentanedione

sulfadimidine - Reference

Reference
Show more
1. Ma Haikuan, Han Xiaohong, Zhang Dihua, etc. Detection and Analysis of sulfonamides in fish by surface enhanced Raman spectroscopy [J]. Acta laser biology Sinica, 2014, 23(006):560-565.
2. Zhao Suhua, fan Hongjie. Serotype identification and drug resistance analysis of avian Escherichia coli in northern Anhui [J]. Journal of Animal Husbandry and Veterinary Medicine, 2017, 49(004):95-98.
3. Zhang Zheng, Li Pan-jie, Jiang Cai-yun, etc. Investigation of metals and antibiotics in municipal wastewater treatment process [J]. Journal of Nanjing Normal University (Engineering and Technology Edition), 2018, 018(002):86-92.
4. Kollinger, Kefei, niudejun, et al. Screening of sulfonamide sensitive strains by UV mutagenesis and its application in the detection of milk sulfonamide antibiotics [J]. Modern food science and technology, 2019, 35(5):296-303.
5. Liu Minfang, Cao mengrui, Li Rongxu, etc. Isolation, identification and drug sensitivity analysis of salmonella from waterfowl in some areas of Guangdong province [J]. Heilongjiang Journal of Animal Science and Veterinary Medicine, 2018(10).
6. Ning Yu, Chen Yu, Yan Zhiming. Sulfonamides in milk based on SNW-1 magnetic solid phase extraction [J]. Fujian Journal of Agricultural Sciences, 2020,35(10):1154-1161.
7. [IF = 19.503] Cheng-Xin Chen et al."Non-covalent self-assembly synthesis of AQ2S@rGO nanocomposite for the degradation of sulfadiazine under solar irradiation: The indispensable effect of chloride."Appl Catal B- Environ. 2021 Dec;298:120495
8. [IF=6.057] Song Hu et al."Reliable performance of aggregation-induced emission nanoparticle-based lateral flow assay for norfloxacin detection in nine types of animal-derived food."Talanta. 2020 Nov;219:121245
9. [IF=6.498] Jingyun Shi et al."Groundwater antibiotics and microplastics in a drinking-water source area, northern China: Occurrence, spatial distribution, risk assessment, and correlation."Environ Res. 2022 Jul;210:112855
10. [IF=4.821] Jin-Ye Lang et al."Preparation of boronate-modified larger mesoporous polymer microspheres with fumed silica nanoparticle and toluene as synergistic porogen for selective separation of sulfonamides."Microchem J. 2022 Apr;175:107193
11. [IF=6.707] Nan Zhang et al."Growth of MOF@COF on corncob as effective adsorbent for enhancing adsorption of sulfonamides and its mechanism."Appl Surf Sci. 2022 Apr;580:152285
12. [IF=7.963] Zikun Dong et al."Mechanism for biodegradation of sulfamethazine by Bacillus cereus H38."Sci Total Environ. 2022 Feb;809:152237
13. [IF=7.312] Yunyun Li et al."Mass transfer enhancement for rapid selective extraction of pharmaceuticals by enlarging the microporous on isostructural zeolitic imidazolate Framework-8."SEPARATION AND PURIFICATION TECHNOLOGY. 2022 Jul;293:121102
14. [IF=5.833] Hu Wenyao et al."Flexible membrane composite based on sepiolite/chitosan/(silver nanoparticles) for enrichment and surface-enhanced Raman scattering determination of sulfamethoxazole in animal-derived food."MICROCHIMICA ACTA. 2022 May;189(5):1-12
15. [IF=3.365] Guo-Ying Chen et al."Nanozyme based on ZIF-8 for the colorimetric detection of sulfonamides in cow milk."ANALYTICAL BIOCHEMISTRY. 2022 Sep;652:114748

sulfadimidine - Nature

Open Data Verified Data

white or yellowish crystalline powder, odorless, slightly bitter taste. Melting point 176 °c. Very slightly soluble in ether and water, soluble in dilute acid or dilute alkali, light color gradually darkened.

Last Update:2025-06-10 22:55:16

sulfadimidine - Preparation Method

Open Data Verified Data

with sulfamidine as raw material, obtained by cyclization with acetylacetone.

Last Update:2022-01-01 10:10:54

sulfadimidine - Introduction

No smell, slightly bitter taste, the color gradually darkens when exposed to light.
Last Update:2022-10-16 17:26:30

sulfadimidine - Application

Open Data Verified Data

used as an antibacterial agent for the prevention and treatment of Staphylococcus and hemolytic Streptococcus infection, suitable for the treatment of hemolytic Streptococcus, meningococcus, Pneumonia cocci and other infections. Mainly used for the treatment of fowl cholera, Fowl typhoid fever, chicken coccidiosis and so on.

Last Update:2025-08-19 16:24:40
sulfadimidine
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Tel: 0086-551-65418684
Email: sales@tnjchem.com
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Mobile: 0086 189 4982 3763
QQ: 2881500840 Click to send a QQ message
Wechat: 189 4982 3763
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CAS: 57-68-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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View History
sulfadimidine
94-20-2
Raw Materials for sulfadimidine
Sodium carbonate
Cyclohexanone
Sulphaguanidine
2,4-Pentanedione
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