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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 4-Nitrobenzhydrazide - ≥98%(HPLC) , CAS No.636-97-5
Synonyms
AB00376454-03 | EN300-18257 | FT-0619209 | p-Nitrobenzohydrazide | BENZOIC ACID, p-NITRO-, HYDRAZIDE | A834477 | NCGC00340686-01 | AZ8HT8UU5S | p-Nitrobenzoic hydrazide | UNII-AZ8HT8UU5S | (4-Nitrobenzoyl)hydrazine | NSC 9804 | 4-Nitrobenzohydrazide | 4-N
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general 4-Nitrobenzoic hydrazide has been used as internal standard in determination of isoniazid in human plasma by LC-MS/MS method.
Specifications Sinónimos
AB00376454-03 | EN300-18257 | FT-0619209 | p-Nitrobenzohydrazide | BENZOIC ACID, p-NITRO-, HYDRAZIDE | A834477 | NCGC00340686-01 | AZ8HT8UU5S | p-Nitrobenzoic hydrazide | UNII-AZ8HT8UU5S | (4-Nitrobenzoyl)hydrazine | NSC 9804 | 4-Nitrobenzohydrazide | 4-N
Especificaciones y pureza
≥98%(HPLC)
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 488194512 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488194512 Sonrisas canónicas C1=CC(=CC=C1C(=O)NN)[N+](=O)[O-] IUPAC Name 4-nitrobenzohydrazide InChIKey FKZXYJYTUSGIQE-UHFFFAOYSA-N INCHI 1S/C7H7N3O3/c8-9-7(11)5-1-3-6(4-2-5)10(12)13/h1-4H,8H2,(H,9,11) Isómeros SMILES C1=CC(=CC=C1C(=O)NN)[N+](=O)[O-] WGK Alemania 3 RTECS DH5670000 Peso molecular 181.15 Beilstein 9(2)274 Reaxy-Rn 519882 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=519882&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Clase Benzene and substituted derivatives Subclass Nitrobenzenes Intermediate Tree Nodes Not available Direct Parent Nitrobenzenes Alternative Parents Benzoic acids and derivatives Nitroaromatic compounds Benzoyl derivatives Carboxylic acid hydrazides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Carboxylic acid hydrazide - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group. External Descriptors C-nitro compound Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solubility in Acetic acid almost transparency;solubility acetone: soluble 0.5 g/10 mL, clear, yellow Sensibilidad Air sensitive Punto de fusión (°C) 218°C Peso molecular 181.150 g/mol XLogP3 0.300 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 181.049 Da Monoisotopic Mass 181.049 Da Topological Polar Surface Area 101.000 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 206.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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