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547-32-0

Basic Information
CAS No.: 547-32-0
Name: Sodium sulfadiazine
Article Data: 4
Molecular Structure:
Molecular Structure of 547-32-0 (Sodium sulfadiazine)
Formula: C10H9N4NaO2S
Molecular Weight: 273.271
Synonyms: Benzenesulfonamide,4-amino-N-2-pyrimidinyl-, monosodium salt (9CI);Sodium, (N1-2-pyrimidinylsulfanilamido)-(7CI);Sulfadiazine, sodium deriv. (6CI);Sulfanilamide, N1-2-pyrimidinyl-,monosodium salt (8CI);2-Sulfanilamidopyrimidine sodium salt;Monosodium2-sulfanilamidopyrimidine;Sodium 2-sulfanilamidopyrimidine;Sodium sulfapyrimidine;Sulfadiazine sodium;Sulfapyrimidine sodium;
EINECS: 208-919-0
Density: 1.496g/cm3
Boiling Point: 512.6oC at 760 mmHg
Flash Point: 263.8oC
Appearance: white to off-white crystalline powder
Hazard Symbols: HarmfulXn
Risk Codes: 22-36/37/38-42/43
Safety: 22-26-36/37-45
Transport Information: UN 3249
PSA: 97.56000
LogP: 2.38040
Synthetic route
68-35-9

sulfadiazine

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water Heating;
12080-32-9

dichloro(1,5-cyclooctadiene)platinum(ll)

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

39234-21-4

sodium N-methyl-N-phenyldithiocarbamate

[Pt(SD)(me-DTC)]

Conditions
ConditionsYield
Stage #1: dichloro(1,5-cyclooctadiene)platinum(ll); poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)] In water for 1h; Reflux;
Stage #2: sodium N-methyl-N-phenyldithiocarbamate In water for 3h; Reflux;
97%
7440-22-4

silver

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

22199-08-2

silver sulfadiazine

Conditions
ConditionsYield
With sodium nitrate; nitric acid In water for 0.1h; Electrochemical reaction; Green chemistry;97%
12080-32-9

dichloro(1,5-cyclooctadiene)platinum(ll)

13074-29-8

(N-ethyl-N'-phenyl-dithiocarbamato) sodium

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

[Pt(SD)(et-DTC)]

Conditions
ConditionsYield
Stage #1: dichloro(1,5-cyclooctadiene)platinum(ll); poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)] In water for 1h; Reflux;
Stage #2: (N-ethyl-N'-phenyl-dithiocarbamato) sodium In water for 3h; Reflux;
92%
5263-87-6

6-methoxy quinoline

cobalt(II) sulphate heptahydrate

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

Co(sulfadiazine)2(6-methoxyquinoline)2

Conditions
ConditionsYield
In methanol for 4h; Reflux;89.1%
298-96-4

triphenyltetrazolium chloride

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

C19H15N4(1+)*C10H9N4O2S(1-)

Conditions
ConditionsYield
In methanol; water at 20℃; for 2h;88%

zinc(II) chloride hexahydrate

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

1096051-46-5

Zn(sulfadiazine)2(H2O)2

Conditions
ConditionsYield
In water aq. Zn salt added to aq. Na salt of sulfadiazine; soln. stirred at 40°C for 3 h; cooled to room temp.; filtered under vac., washed with water; dried over CaCl2; elem. anal.;87%

zinc(II) acetate tetrahydrate

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

1096051-46-5

Zn(sulfadiazine)2(H2O)2

Conditions
ConditionsYield
In water aq. Zn salt added to aq. Na salt of sulfadiazine; soln. stirred at 40°C for 3 h; cooled to room temp.; filtered under vac., washed with water; dried over CaCl2;87%
21264-30-2, 90243-59-7, 14592-56-4

dichloro bis(acetonitrile) palladium(II)

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

39234-21-4

sodium N-methyl-N-phenyldithiocarbamate

[Pd(SD)(me-DTC)]

Conditions
ConditionsYield
Stage #1: dichloro bis(acetonitrile) palladium(II); poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)] In water for 1h; Reflux;
Stage #2: sodium N-methyl-N-phenyldithiocarbamate In water for 3h; Reflux;
85%

[Fe(N-(2-hydroxybenzyl)-N-(2-pyridylmethyl)(3-chloro)(2-hydroxy)propylamine)Cl2]*H2O

547-32-0

poly[{μ3-4-[(pyrimidin-2-ylazanidyl)sulfonyl]aniline}sodium(I)]

[(Cl)(sulfadiazine)Fe(III)(μ-N-(2-hydroxybenzyl)-N-(2-pyridylmethyl)(3-chloro)(2-hydroxy)propylamine)2Fe(III)(sulfadiazine)(Cl)]*2H2O

Conditions
ConditionsYield
In methanol; water Reflux;85%
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Specification

This chemical is called Sulfadiazine Sodium, and its CAS registry number is 547-32-0. With the molecular formula of C10H9N4NaO2S, its classification codes are Antibacterial; Drug / Therapeutic Agent; Mutation data; Reproductive Effect. Additionally, it's used for cure sulfonamide, susceptible infections and it can also be used for T. gondii infection. However, it should be stored at 2-8°C.

Other characteristics of the Sulfadiazine Sodium can be summarised as followings: (1)#H bond acceptors: 6; (2)#H bond donors: 3; (3)#Freely Rotating Bonds: 2; (4)Polar Surface Area: 106.35 Å2.

When you are using this chemical, please be cautious about it as the following: This chemical is irritating to eyes, respiratory system and skin. It may cause sensitization by inhalation and skin contacting. You should wear suitable protective clothing if you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice. 

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 1747mg/kg (1747mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 81, Pg. 17, 1944.
mouse LD50 intravenous 540mg/kg (540mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 94, Pg. 338, 1953.
mouse LD50 oral 1700mg/kg (1700mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 94, Pg. 338, 1953.
mouse LD50 subcutaneous 1408mg/kg (1408mg/kg)   Acta Medica Scandinavica, Supplement. Vol