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Home > Encyclopedia > Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1)

Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1)

pharmaceutical raw materials
Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1) structure

Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1) 

structure
  • CAS No:

    127-58-2

  • Formula:

    C11H12N4O2S.Na

  • Chemical Name:

    Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1)

  • Synonyms:

    Benzenesulfonamide,4-amino-N-(4-methyl-2-pyrimidinyl)-,sodium salt (1:1);Sulfanilamide,N1-(4-methyl-2-pyrimidinyl)-,monosodium salt;Benzenesulfonamide,4-amino-N-(4-methyl-2-pyrimidinyl)-,monosodium salt;Sodium,[N1-(4-methyl-2-pyrimidinyl)sulfanilamido]-;Sulfamerazine,sodium deriv.;Monosodium 2-sulfanilamido-4-methylpyrimidine;Sodium sulfamerazine;Soluble sulfamerazine;Sulfamerazine sodium;2-Sulfanilamido-4-methylpyrimidine sodium salt;4-Methyl-2-sulfanilamidopyrimidine sodium salt;Solumedine;Sulfamerazine sodium Salt

  • Categories:

    Active Pharmaceutical Ingredients  >  Synthetic Anti-infective Drugs

Description

Sulfamerazine Sodium is a sulfonamide antibacterial.Target: AntibacterialSulfamerazine, the monomethyl derivative of sulfadiazine, is 2-sulfanilamido-4-methylpyrimidine. Sulfamerazine is a sulfonamide drug that inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA) for binding to dihydropteroate synthetase (dihydrofolate synthetase). Sulfamerazine is bacteriostatic in nature. Inhibition of dihydrofolic acid synthesis decreases the synthesis of b


Sulfamerazine Sodium is a sodium salt form of sulfamerazine, a long-acting sulfanilamide antibacterial agent.

Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1) Basic Attributes

286.29

286.050049

204-851-0

JOV4UJY07O

DTXSID1051644

C80794

Characteristics

97.56000

2.68880

216-219 °C

519.1ºC at 760mmHg

267.8ºC

Safety Information

NONH for all modes of transport

3

20/22-36/38-36/37/38

7-24-45-36-26

WP0760000

Xn,Xi

P305 + P351 + P338

H302-H315-H319-H332

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, and P501|Aggregated GHS information provided by 42 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1) Use and Manufacturing

Uses

Involved in characterization of chirosan membranes for the transport of drugs1,2,3

Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, sodium salt (1:1): INACTIVE

Computed Properties

Molecular Weight:286.29
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:286.05004106
Monoisotopic Mass:286.05004106
Topological Polar Surface Area:95.3
Heavy Atom Count:19
Complexity:365
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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