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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Hansa Yellow - ≥45.0%(E) , CAS No.2512-29-0
Synonyms
Hansa Yellow G Extra | UNII-RMB4YA40UY | Acrylamide Yellow G | alpha-(o-Nitro-p-tolylazo)acetoacetanilide | Hansa Yellow Toner G YA-8365 | Symuler Fast Yellow GH | Lightfast Yellow | Transa Flo Yellow | D90834 | JAPAN YELLOW NO. 401 | Toluidine Yellow AH
Storage
Protected from light,Room temperature,Desiccated
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Why this grade ≥45.0%(E) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Room temperature,Desiccated Ships Normal 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.
Specifications Sinónimos
Hansa Yellow G Extra | UNII-RMB4YA40UY | Acrylamide Yellow G | alpha-(o-Nitro-p-tolylazo)acetoacetanilide | Hansa Yellow Toner G YA-8365 | Symuler Fast Yellow GH | Lightfast Yellow | Transa Flo Yellow | D90834 | JAPAN YELLOW NO. 401 | Toluidine Yellow AH
Especificaciones y pureza
≥45.0%(E)
Condiciones de almacenamiento de almacenamiento
Protected from light,Room temperature,Desiccated
Nombres e identificadores Sonrisas canónicas
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=CC=CC=C2)[N+](=O)[O-]
IUPAC Name
2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-N-phenylbutanamide
InChIKey
MFYSUUPKMDJYPF-UHFFFAOYSA-N
INCHI
1S/C17H16N4O4/c1-11-8-9-14(15(10-11)21(24)25)19-20-16(12(2)22)17(23)18-13-6-4-3-5-7-13/h3-10,16H,1-2H3,(H,18,23)
Isómeros SMILES
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=CC=CC=C2)[N+](=O)[O-]
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1844988&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 Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acid amides Alternative Parents Anilides Nitrotoluenes Nitrobenzenes Nitroaromatic compounds N-arylamides 1,3-dicarbonyl compounds Fatty amides Secondary carboxylic acid amides Azo compounds Ketones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic zwitterions Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Alpha-amino acid amide - Nitrobenzene - Anilide - Nitrotoluene - Nitroaromatic compound - N-arylamide - Toluene - Monocyclic benzene moiety - Fatty amide - 1,3-dicarbonyl compound - Benzenoid - Fatty acyl - Organic nitro compound - Carboxamide group - Ketone - Azo compound - C-nitro compound - Secondary carboxylic acid amide - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxygen compound - Organic oxide - Organic zwitterion - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. External Descriptors Not available 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 Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Light and Moisture sensitive Peso molecular 340.330 g/mol XLogP3 3.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 340.117 Da Monoisotopic Mass 340.117 Da Topological Polar Surface Area 117.000 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 525.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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