The store will not work correctly when cookies are disabled.
O JavaScript parece estar desativado no seu browser. Para usufruir da melhor experiência no nosso site, certifique-se que ativa o JavaScript no seu browser.
· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Hansa Amarelo - ≥45.0%(E) , CAS No.2512-29-0
Disponível para encomenda
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
Protegido da luz,Temperatura ambiente,Dessecado
🧪
Why this grade ≥45.0%(E) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Protegido da luz,Temperatura ambiente,Dessecado Ships Normal Check lot-specific COA for exact specifications.
📋
Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
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
Especificações e pureza
≥45.0%(E)
Condições de armazenamento de armazenamento
Protegido da luz,Temperatura ambiente,Dessecado
Nomes e identificadores Sorrisos canónicos
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)
SMILES isoméricas
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 Classe 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 Descrição 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.
Estrutura 3D Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade 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
Calculadoras de soluções Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Revisões
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Definições Concordo com tudo Decline
Shall we send you a message when we have discounts available?
Remind me later Autorizar
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
H2508442