363634
Semicarbazide
6 wt. % (on silica gel)
Synonyme(s) :
Aminourea, Hydrazinecarboxamide, Isosemicarbazide
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About This Item
Formule linéaire :
H2NCONHNH2
Numéro CAS:
Poids moléculaire :
75.07
Numéro MDL:
Code UNSPSC :
12352125
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Application
- Antibacterial activity: Semicarbazide derivatives, specifically thiosemicarbazide, exhibit significant antibacterial properties influenced by substituent position. This underscores its application in pharmaceutical synthesis and microbial resistance studies (Janowska et al., 2024).
- Solar cell performance: The application of semicarbazide hydrochloride in suppressing deep-level traps significantly improves the efficiency of tin-based perovskite solar cells, highlighting its potential in energy materials research (Jia et al., 2023).
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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The relationship between the soluble copper topaquinone amine oxidases, the membrane bound semicarbazide-sensitive amine oxidases and lysyl oxidase remains unclear. The stereochemical course of substrate oxidation has been determined for each enzyme type and these studies suggest that SSAO and
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Semicarbazide-sensitive amine oxidase (SSAO), identical to primary amine oxidase or vascular adhesion protein-1, is a membrane enzyme that generates hydrogen peroxide. SSAO is highly expressed at the adipocyte surface, and its plasma levels increase with type 2 diabetes. Since visceral
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