BDBM50108606. It is a water-soluble white solid. Visit ChemicalBook To find more Semicarbazide hydrochloride(563-41-7) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. WGK Germany: 3, Please post your buying leads,so that our qualified suppliers will soon Semicarbazide hydrochloride is a general reagent used to synthesize semicarbazones from aldehydes and ketones. BDBM50108606. Human systemic effects by intravenous route: convulsions. semicarbazide group. CARBAMOHYDRAZONIC ACID. semicarbazide group. Semicarbazide hydrochloride is a general reagent used to synthesize semicarbazones from aldehydes and ketones. Semicarbazide is the chemical compound with the formula OC(NH2)(N2H3). Semicarbazide products (semicarbazones and thiosemicarbazones) are known to have an activity of antiviral, antiinfective and antineoplastic through binding to copper or iron in cells. BBL012207. BBL012207. See also HYDRAZINE. Flash Point: 66.5 °C Boiling Point: 186.3 °C at 760 mmHg Vapour Pressure: 0.187 mmHg at 25°C Enthalpy of Vaporization: 49.18 kJ/mol Following is the molecular structure of Semicarbazide … CTK4I8064. Contact: +49 (0) 34291 337236! It is a derivative of urea. CARBAMOHYDRAZONIC ACID. Isosemicarbazide(8CI); Aminourea; Carbamic acid, hydrazide; Carbamylhydrazine; Carbazamide;Carbazimidic acid; Hydrazine, (aminocarbonyl)-; Semicarbazide; Urea, amino-. CTK1H0745. [4]. Packaging 100, 500 g … Semicarbazide, 6 wt% on Silica gel. It is a water-soluble white solid. Semicarbazide is the chemical compound with the formula OC(NH2)(N2H3). A further reaction can occur to give carbohydrazide: Semicarbazide is frequently reacted with aldehydes and ketones to produce semicarbazones via a condensation reaction. Chemistry informtion about Semicarbazide (57-56-7) is: IUPAC Name: Aminourea Synonyms: Aminomocovina ; Amino-Ure ; Carbamic Acid, Hydrazide ; Carbamicacid,Hydrazide ; Carbamoyl-Hydrazin ; Carbamylhydrazine ; Carbazamide ; Hydrazine, Carbamoyl- MF: CH5N3O MW: 75.07 EINECS: 200-339-6  Density: 1.286 g/cm3 Flash Point: 66.5 °C Boiling Point: 186.3 °C at 760 mmHg Vapour Pressure: 0.187 mmHg at 25°C Enthalpy of Vaporization: 49.18 kJ/mol Following is the molecular structure of  Semicarbazide (57-56-7) is: Semicarbazide (57-56-7) is used as a detection reagent on thin layer chromatography (TLC). It is a derivative of urea. In addition, the reaction could achieve 75% yield of 3 a when the solvent, acetic acid, replaced by higher boiling point and weaker acidic n‐butyric acid (entry 18). 13C, 15N2-Semicarbazide hydrochloride | Buy from the Brand Leader in Analytical Reference Standards! Why ? ©2008 LookChem.com,License:ICP NO. The compound prepared by treating urea with hydrazine:[1]. InChI=1S/CH5N3O/c2-1(5)4-3/h3H2,(H3,2,4,5), InChI=1/CH5N3O/c2-1(5)4-3/h3H2,(H3,2,4,5), Except where otherwise noted, data are given for materials in their. It can also be used to prepare corrosion inhibitors. The reaction could finally achieve 90% yield by increasing the loading of both AgTFA and 2 a to 3 equiv. Journal of Pharmacology and Experimental Therapeutics. Lopac-S-2201. Semicarbazide (SEM) carbamic acid hydrazide. Vol. Jean-Pierre Schirmann, Paul Bourdauducq "Hydrazine" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. Packaging 100, 500 g … 444, 1957. All India 2012) Answer: ... NH 2 in semicarbazide is involved in the resonance with -CO-group. contact you! ZINC8035043. Journal of Pharmacology and Experimental Therapeutics. This is an example of imine formation resulting from the reaction of a primary amine with a carbonyl group. Hazard Codes: Xn: Harmful Risk Statements: R22: Harmful if swallowed. When heated to decomposition it emits toxic fumes of NO. Vol. (b) Compound C 9 H 10 O forms 2, 4-DNP derivative, so it contains a carbonyl group. Guidechem provides Semicarbazide hydrochloride chemical database query, including CAS registy number 563-41-7, Semicarbazide hydrochloride MSDS (Material Safety Data Sheet), nature, English name, manufacturer, function/use, molecular weight, density, boiling point, melting point, structural formula, etc. Flash Point: 66.5 °C Boiling Point: 186.3 °C at 760 mmHg Vapour Pressure: 0.187 mmHg at 25°C Enthalpy of Vaporization: 49.18 kJ/mol Following is the molecular structure of Semicarbazide … nitrofuran antibacterials (furazolidone, nitrofurazone, nitrofurantoin), and dizatrifone. Semicarbazide forms in heat-treated flour containing ADC as well as breads made from ADC-treated flour. When heated to decomposition it emits toxic fumes of NOx. 110, 1958. points; solids appear last in each table in order of increasing melting points. Vol. Lopac0_001096. Melting Point (°C) 101 - 200 (11) 201 - 300 (6) Color. of 1 a (entry 19). 122, Pg. Semicarbazide stains α-keto acids on the TLC plate, which can then be viewed under ultraviolet light. Aldehydes and Ketones have lower boiling points than corresponding alcohols. [3] 296, 1967. ZINC8035043. Mutation data reported. The reaction is useful because semicarbazones, like oximes and 2,4-DNPs, typically have high melting points and crystallize, facilitating purification or identification of reaction products.[2]. Compounds are arbitrarily listed by increasing boiling points unless their melting points are above 40°C. 4-03-00-00177 (Beilstein Handbook Reference) [N]NC(N)=O. Made in Germany! Naunyn-Schmiedebergs Archiv fuer Pharmakologie und Experimentelle Pathologie. 257, Pg. Safety Statements: S22: Do not breathe dust. It is also a product of degradations of the blowing agent azodicarbonamide (ADC). It can also be used to prepare corrosion inhibitors. 4-03-00-00177 (Beilstein Handbook Reference) [N]NC(N)=O. Questionable carcinogen with experimental tumorigenic data. Semicarbazide is used in preparing pharmaceuticals including: (Comptt. Mutation data reported. gas chromatography (GC) (5) HPLC (5) immunohistochemistry (1) UV/Vis spectroscopy (1) ... Summary: This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Lopac0_001096. CTK1H0495. You can also browse global suppliers,vendor,prices,Price,manufacturers of Semicarbazide hydrochloride(563-41-7). It can be used to build a variety of heterocyclic compounds, some of which are potent antimicrobial and antiviral agents. Semicarbazide is used as a detection reagent in thin layer chromatography (TLC). CTK1H0745. 119, Pg. Antibody Enhanced Validation (1) Application. Hydrazinecarboximidicacid (9CI) DTXSID7043823. Semicarbazide, 6 wt% on Silica gel. :Zhejiang16009103. Semicarbazide (SEM) carbamic acid hydrazide.