Aniline solution - analytical standard, 0.989 mg/ml in methanol , CAS No.62-53-3

CAS: 62-53-3 Cat. No.: A117355 Fórmula: C6H5NH2 Peso molecular: 93.13 Beilstein Registry Number: 605631 Número CE: 200-539-3
Disponível para encomenda
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 0.989 mg/ml in methanol
Synonyms
ANILINE|Benzenamine|Phenylamine|62-53-3|Aminobenzene|Aminophen|Arylamine|Kyanol|Anilin|Cyanol|Benzeneamine|Krystallin|Benzidam|Anyvim|Anilina|Huile D'aniline|C.I. Oxidation Base 1|Rcra waste number U012|CI Oxidation Base 1|Caswell No. 051C|Anilinum|C.I. 7
Storage
Store at 2-8°C
Shipped In
Wet ice,FedEx DG Service
★
Size
USA
Alemanha (EU)*
Price
Qty
2ml
A117355-2ml
2 Em stock
—

65,90US$

77,90US$
Gravar 12,00 US$ (15.40%)
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Why this grade

analytical standard, 0.989 mg/ml in methanol Padrão analítico for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice,FedEx DG Service 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 1366 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
ANILINE | Benzenamine | Phenylamine | 62-53-3 | Aminobenzene | Aminophen | Arylamine | Kyanol | Anilin | Cyanol | Benzeneamine | Krystallin | Benzidam | Anyvim | Anilina | Huile D'aniline | C.I. Oxidation Base 1 | Rcra waste number U012 | CI Oxidation Base 1 | Caswell No. 051C | Anilinum | C.I. 7
Especificações e pureza
analytical standard, 0.989 mg/ml in methanol
Condições de armazenamento de armazenamento
Store at 2-8°C
Enviado em
Wet ice,FedEx DG Service
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Grau
Padrão analítico
Nomes e identificadores
Pubchem Sid
Sorrisos canónicos
C1=CC=C(C=C1)N
IUPAC Name
aniline
InChIKey
PAYRUJLWNCNPSJ-UHFFFAOYSA-N
INCHI
1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2
SMILES isoméricas
C1=CC=C(C=C1)N
WGK Alemanha
1
Número UN
1547
Grupo de embalagem
II
Peso molecular
93.13
Beilstein
605631
Reaxy-Rn
605631
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605631&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassAniline and substituted anilines
Intermediate Tree Nodes Not available
Direct ParentAniline and substituted anilines
Alternative Parents Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors an arylamine
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2E1 Tchem Cytochrome P450 2E1 (2174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lithobates pipiens (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-22 (3261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
E Lysozyme (95 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colon (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDataItem
G2015002Certificate of AnalysisJan 30, 2024 A117355
G2207037Certificate of AnalysisJun 16, 2022 A117355
Propriedades químicas e físicas
SensibilidadeLight sensitive.
Índice de refração1.5863
Ponto de inflamação (°C)76℃
Ponto de ebulição (°C)184-186°C
Ponto de fusão (°C)-6°C
Peso molecular93.130 g/mol
XLogP30.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass93.0578 Da
Monoisotopic Mass93.0578 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count7
Formal Charge0
Complexity46.100
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs e artigos
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Enzyme Labels in Immunoassays, Signal Amplification, and Multi-Enzyme Detection Platforms: A Functional Overview
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Polyetherimide (PEI): Structural Features, Main Properties, and Typical Application Directions
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
From Natural Cellulose to Nanocrystals: Structural Characteristics, Application Directions, and Industrialization Challenges of CNC
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
One-Pot Deaminative Cyanation of Arylamines Mediated by Nitrate Reduction: The ORT Pathway and Kinetic Matching of Tandem Reaction Steps
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Bond-Forming Reactions of N-Sulfinylamine and the Synthesis of S(VI) Functional Groups: Two-Electron Addition, Radical Addition, and Formal Cycloaddition
Desaturative Amination for the Synthesis of Amino Heteroarenes: Carbonyl-Site Predefinition of the C–N Bond-Forming Position and Subsequent Desaturative Aromatization
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Citations of This Product
Calculadoras de soluções
Revisões

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