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Sulfamerazine sodium

Sulfamerazine sodium Structure
CAS No.
127-58-2
Chemical Name:
Sulfamerazine sodium
Synonyms
Nsc226823;solumedine;sulfamerazine sodium;SODIUM SULFAMERAZINE;sodiumsulphamerazine;solublesulfamerazine;Pyrimidine sodium sulfa;SULFAMERAZINE SODIUM SALT;SulfadimidineSodium,Pharma;Sulfamerazine sodium USP/EP/BP
CBNumber:
CB9289260
Molecular Formula:
C11H13N4NaO2S
Molecular Weight:
288.3
MOL File:
127-58-2.mol
MSDS File:
SDS
Modify Date:
2024/4/3 12:01:51

Sulfamerazine sodium Properties

RTECS WP0760000
storage temp. Store at -20°C
solubility Soluble in DMSO
form Powder
Water Solubility Soluble in DMSO or water
CAS DataBase Reference 127-58-2(CAS DataBase Reference)
EPA Substance Registry System Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, monosodium salt (127-58-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302+H332-H315-H319
Precautionary statements  P261-P264-P301+P312-P302+P352-P304+P340+P312-P305+P351+P338
Hazard Codes  Xn,Xi
Risk Statements  20/22-36/38-36/37/38
Safety Statements  7-24-45-36-26
WGK Germany  3
TSCA  Yes
NFPA 704
0
3 0

Sulfamerazine sodium price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S0800 Sulfamerazine sodium salt 127-58-2 250G ₹9471.88 2022-06-14 Buy
Product number Packaging Price Buy
S0800 250G ₹9471.88 Buy

Sulfamerazine sodium Chemical Properties,Uses,Production

Description

Sulfamerazine is a sulfonamide antibiotic. It inhibits bacterial carbonic anhydrase by ~20% at a concentration of 500 μM. In vivo, sulfamerazine (500 mg/L) reduces severity of peribronchitis and inhibits cilia-associated respiratory Bacillus colonization in mice. It also prevents death of Toxoplasma-infected mice. Sulfonamide class antibiotics, of which sulfamerazine is a member, are bacteriostatic and inhibit bacterial synthesis of dihydrofolic acid by competing with 4-aminobenzoic acid for binding to dihydropteroate synthase. Formulations containing sulfamerazine have been used for the treatment of pneumonia and typhoid fever.

Uses

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

World Health Organization (WHO)

Sulfamerazine sodium, a sulfonamide anti-infective agent, was introduced several decades ago for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing resistance and their replacement by antibiotics which are generally more active and less toxic. The sulfonamides are known to cause serious adverse effects such as renal toxicity, sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Sulfamerazine is still used in some countries usually in combination with other sulfonamides.

Safety Profile

Moderately toxic by ingestion, subcutaneous, intraperitoneal, and intravenous routes. When heated to decomposition it emits toxic fumes of SOx, NOx, and Na2O.

Sulfamerazine sodium Preparation Products And Raw materials

Raw materials

Preparation Products

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solumedine SODIUM SULFAMERAZINE sulfamerazine sodium SULFAMERAZINE SODIUM SALT SULFAMERAZINE, SODIUM SALT MONOHYDRATE monosodium 2-sulfanilamido-4-methylpyrimidine 2-sulfanilamido-4-methylpyrimidine sodium salt 4-AMINO-N-[4-METHYL-2-PYRIMIDINYL]-BENZENESULFONAMIDE SODIUM SALT 4-methyl-2-sulfanilamidopyrimidine sodium salt 4-amino-n-(4-methyl-2-pyrimidinyl)-benzenesulfonamidmonosodiumsalt n(sup1)-(4-methyl-2-pyrimidinyl)sulfanilamidesodiumsalt n(sup1)-(4-methyl-2-pyrimidinyl)-sulfanilamidmonosodiumsalt sodiumsulphamerazine solublesulfamerazine SULFAMERAZINE SODIUM(SM1-NA)(NDC:56631-1715) Pyrimidine sodium sulfa SulfadimidineSodium,Pharma Benzenesulfonamide, 4-amino-N-(4-methyl-2-pyrimidinyl)-, monosodium salt Nsc226823 (4-aminophenyl)sulfonyl-(4-methylpyrimidin-2-yl)azanide sodium,(4-aminophenyl)sulfonyl-(4-methylpyrimidin-2-yl)azanide Sulfamerazine sodium USP/EP/BP 127-58-2 C11H11N4NaO2S C11H11N4O2SNa Heterocyclic Building Blocks Pyrimidines Building Blocks Building Blocks C9 to C11 Chemical Synthesis Heterocyclic Building Blocks Pyrimidines