CAS 57-56-7

Semicarbazide

Description:

Semicarbazide is an organic compound characterized by its hydrazine derivative structure, featuring a semicarbazide functional group. It is typically encountered as a white crystalline solid that is soluble in water and alcohol, making it relatively easy to handle in laboratory settings. Semicarbazide is known for its role as a reagent in organic synthesis, particularly in the formation of semicarbazones, which are important intermediates in the synthesis of various pharmaceuticals and agrochemicals. The compound exhibits moderate stability under standard conditions but can decompose upon exposure to strong acids or bases. Semicarbazide is also recognized for its potential biological activity, including its use in the study of certain metabolic pathways. However, it is important to handle this substance with care, as it may pose health risks, including potential toxicity and irritant effects. Proper safety protocols should be followed when working with semicarbazide in any chemical research or industrial application.

Formula: CH₅N₃O

InChI: InChI=1S/CH5N3O/c2-1(5)4-3/h3H2,(H3,2,4,5)

InChI key: InChIKey=DUIOPKIIICUYRZ-UHFFFAOYSA-N

SMILES: C(NN)(N)=O

Synonyms:

• Aminourea
• Carbamic acid, hydrazide
• Carbamylhydrazine
• Carbazamide
• Carbazimidic acid
• Hydrazine, (aminocarbonyl)-
• Isosemicarbazide
• Semicarbazid
• Semicarbazida
• Semicarbazide
• Urea, amino-

Semicarbazide, 6 wt% on Silica gel

CAS: 57-56-7

Formula: CH₅N₃O

Purity: %

Color and Shape: Solid

Molecular weight: 75.0699

Ref: IN-DA00371U

Hydrazinecarboxamide

CAS: 57-56-7

Hydrazinecarboxamide

Purity: 6 wt. % (on silica gel)

Molecular weight: 75.07g/mol

Ref: 54-OR1025063

Hydrazinecarboxamide

CAS: 57-56-7

Purity: 95.0%

Molecular weight: 75.07099914550781

Ref: 10-F448575

Semicarbazide - 6 wt% on Silica gel

CAS: 57-56-7

Semicarbazide is a coumarin derivative that inhibits the growth of bacteria. It is used as an antimicrobial agent, and has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. Semicarbazide has been found to have significant cytotoxicity in the presence of NADH and acetate, but not in the presence of glucose or oxygen. The mechanism of its cytotoxicity is thought to be due to its ability to inhibit enzymes such as alcohol dehydrogenase, aminopeptidase, and glutathione reductase. Semicarbazide also inhibits the growth of certain types of cancer cells by inhibiting DNA synthesis and protein synthesis. This substance has been successfully used in animal studies for the treatment of heart disease by reducing blood pressure and increasing coronary flow velocity.

Formula: CH₅N₃O

Purity: Min. 95%

Molecular weight: 75.07 g/mol

Ref: 3D-FS143227