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

CAS: 62-53-3 Cat. No.: A117355 Formula: C6H5NH2 Molecular Weight: 93.13 Beilstein Registry Number: 605631 EC Number: 200-539-3
1366 Citations COA
Aniline solution - analytical standard, 0.989 mg/ml in methanol CAS No(62-53-3) by Aladdin Scientific
AVAILABLE TO ORDER
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
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Size
USA
Germany (EU)*
Price
Qty
2ml
A117355-2ml
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews
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Why this grade

analytical standard, 0.989 mg/ml in methanol Analytical standard 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

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
Specifications & Purity
analytical standard, 0.989 mg/ml in methanol
Storage
Store at 2-8°C
Shipped In
Wet ice,FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Analytical standard
Names and Identifiers
Pubchem Sid
508816448
Canonical Smiles
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
Isomeric SMILES
C1=CC=C(C=C1)N
WGK Germany
1
UN Number
1547
Packing Group
II
Molecular Weight
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
ClassBenzene 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
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
Mechanisms of Action
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
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 TypeDateItem
G2015002Certificate of AnalysisJan 30, 2024 A117355
G2207037Certificate of AnalysisJun 16, 2022 A117355
Chemical and Physical Properties
SensitivityLight sensitive.
Refractive Index1.5863
Flash Point(°C)76℃
Boil Point(°C)184-186°C
Melt Point(°C)-6°C
Molecular Weight93.130 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
Documents & Articles
Make “Aryl Chlorides + Low Pd Loading + Scale-Up Reproducibility” Reliable: The Initiation and Durability Logic of Pd–NHC (Palladium–N-Heterocyclic Carbene) Cross-Coupling (with Selection Navigation and Product Tables)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Ligand Nitrogen-containing heterocycles
Enzyme Labels in Immunoassays, Signal Amplification, and Multi-Enzyme Detection Platforms: A Functional Overview
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Multiplex detection Methodological Quality Control Enzyme Labels Signal Amplification Immunoassay Chemiluminescence Kinetic Quantification Enzyme Cascades
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Cross-coupling Haloheterocycles
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
AAAs β-Acyloxy Alkenyl Amides
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Amide bond formation Amidation reaction
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
ATD-DMAP
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Amidation reaction TCFH–NMI Amide bond construction
How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Medicinal Chemistry Functional Group Synthetic Intermediate
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
carbamate Boc₂O Boc protection
Polyetherimide (PEI): Structural Features, Main Properties, and Typical Application Directions
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
PEI Polyetherimide
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Organic synthesis Triphosgene
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Amide bond formation carboxylic acid activation
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
ADMP Organic azides
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Cross-coupling Cross-coupling reactions
From Natural Cellulose to Nanocrystals: Structural Characteristics, Application Directions, and Industrialization Challenges of CNC
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Nanocrystalline Natural Cellulose Cellulose Nanocrystals
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
ABCAs azabicyclo[x.1.1]alkanes
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Photocatalysts Saturated quaternary ring Skeleton
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Amidation reaction
One-Pot Deaminative Cyanation of Arylamines Mediated by Nitrate Reduction: The ORT Pathway and Kinetic Matching of Tandem Reaction Steps
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Functional Group Arylnitrile
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
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Azetidine Drug synthesis stereospecificity ring strain regioselectivity N-substituent effects β-substituted amines Aziridine Enantioconvergence Cross-Electrophile Coupling
Bond-Forming Reactions of N-Sulfinylamine and the Synthesis of S(VI) Functional Groups: Two-Electron Addition, Radical Addition, and Formal Cycloaddition
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Organic synthesis Medicinal Chemistry Functional Groups
Desaturative Amination for the Synthesis of Amino Heteroarenes: Carbonyl-Site Predefinition of the C–N Bond-Forming Position and Subsequent Desaturative Aromatization
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
aminopyridines aminopyrroles aminofurans aminothiophenes
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Drugs Aryl C–N
Citations of This Product
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