m-Anisidine - ≥98% , CAS No.536-90-3

CAS: 536-90-3 Cat. No.: A107482 Formule: C7H9NO Poids moléculaire: 123.15 Beilstein Registry Number: 386119 Numéro CE: 208-651-4
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%
Synonyms
FT-0628164 | 3-methoxy-benzenamine | 3-Aminoanisole | EN300-19067 | 3-Methoxy aniline | NCGC00091221-02 | 3-methyoxy-aniline | m-Methoxyaniline | 3-Anisidine | 3-Methoxy-1-aminobenzene | Benzenamine, 3-methoxy- | CCRIS 5886 | SCHEMBL66692 | 3-methoxypheny
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice,FedEx DG Service
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Size
Allemagne (EU)
USA*
Price
Qty
25g
A107482-25g
—
4 En stock
12,06€
100g
A107482-100g
—
En stock ≥10
29,42€
500g
A107482-500g
—
4 En stock
99,70€
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice,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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

 The unusually large amount of dibromo product produced upon bromination of m-anisidine may be attributed to the two doubly activeated positions. The best enantioselectivity of 97 % ee was observed for the reaction of m-anisidine in organocatalytic asymmetric three-component cyclization of cinnamaldehydes and primary amines with 1, 3-Dicarbonyl Compounds. Evidence for the control of 2nd-harmonic generation activities from the x-ray crystal-structures of the complexes of l-tartaric acid with m-anisidine and p-toluidine was determined.

Specifications

Synonymes
FT-0628164 | 3-methoxy-benzenamine | 3-Aminoanisole | EN300-19067 | 3-Methoxy aniline | NCGC00091221-02 | 3-methyoxy-aniline | m-Methoxyaniline | 3-Anisidine | 3-Methoxy-1-aminobenzene | Benzenamine, 3-methoxy- | CCRIS 5886 | SCHEMBL66692 | 3-methoxypheny
Spécifications et pureté
≥98%
Conditions de stockage de stockage
Store at 2-8°C,Argon charged
Expédié en
Wet ice,FedEx DG Service
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥98%
Noms et identifiants
Pubchem Sid504752010
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504752010
Sourires canoniquesCOC1=CC=CC(=C1)N
IUPAC Name3-methoxyaniline
InChIKeyNCBZRJODKRCREW-UHFFFAOYSA-N
INCHI1S/C7H9NO/c1-9-7-4-2-3-6(8)5-7/h2-5H,8H2,1H3
Isomères SMILES COC1=CC=CC(=C1)N
WGK Allemagne 3
RTECS BZ5408000
Numéro ONU 2431
Groupe d'emballage III
Poids moléculaire 123.15
Beilstein 386119
Reaxy-Rn 386119
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=386119&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
ClassePhenol ethers
SubclassAminophenyl ethers
Intermediate Tree Nodes Not available
Direct ParentAminophenyl ethers
Alternative Parents Methoxyanilines  Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aminophenyl ether - Methoxyaniline - Phenoxy compound - Anisole - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aminophenyl ethers. These are aromatic compounds that contain a phenol ether, which carries an amine group on the benzene ring.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

13 results found

Lot NumberCertificate TypeDateArticle
K2120013Certificate of AnalysisSep 04, 2025 A107482
B2513336Certificate of AnalysisJan 16, 2025 A107482
B2513338Certificate of AnalysisJan 16, 2025 A107482
B2513339Certificate of AnalysisJan 16, 2025 A107482
B2513340Certificate of AnalysisJan 16, 2025 A107482
D2113072Certificate of AnalysisJan 08, 2025 A107482
J2026167Certificate of AnalysisAug 19, 2024 A107482
B2302619Certificate of AnalysisJan 02, 2023 A107482
B2302622Certificate of AnalysisJan 02, 2023 A107482
B2302648Certificate of AnalysisJan 02, 2023 A107482
B2302669Certificate of AnalysisJan 02, 2023 A107482
B2324293Certificate of AnalysisNov 06, 2021 A107482
H2224252Certificate of AnalysisNov 06, 2021 A107482

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Propriétés chimiques et physiques
SolubilitéSoluble in water(18g/L).
SensibilitéLight sensitive;Air sensitive;Heat sensitive
Indice de réfraction1.581
Point d'éclair (°F)258.8 °F
Point d'éclair (°C)126 °C
Point d'ébullition (°C)251°C
Point de fusion (°C)-1-1°C
Poids moléculaire123.150 g/mol
XLogP30.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass123.068 Da
Monoisotopic Mass123.068 Da
Topological Polar Surface Area35.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity85.000
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
FAQ et articles
Citations of This Product
Références
1. Yiran Xu, Hongyan Yao, Hao Su, Bo Jiang, Kaixiang Shi, Weixing Song, Shiyang Zhu, Shaowei Guan, Ying Song.  (2023)  Donor-acceptor hyperbranched copolyimides contain different linear segment for electrochromic and resistive memory devices.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2023.107572]
2. Chongyang Zhang, Mengzhu Li, Handong Sun, Xigui Yue.  (2021)  Breath figure-derived porous fluorine-containing poly(ether sulfone) membranes with low dielectric constant.  POLYMER INTERNATIONAL,  70  (10): (1456-1464).  [PMID:] [10.1002/pi.6217]
3. Meng Ruan, Qiqin Wang, Huihui Wu, Yuqiang Wang, Hai Han, Zhengjin Jiang.  (2017)  Preparation and evaluation of tert-leucine derivative functionalized polymeric monoliths for micro-liquid chromatography.  ELECTROPHORESIS,      [PMID:28722219] [10.1002/elps.201700176]
4. Xue Wang, Buyuan Guan, Yapeng He, Dong An, Ye Zhang, Yu Cao, Xiang Li, Yunling Liu, Qisheng Huo.  (2015)  Megranate-like nanoreactor with multiple cores and an acidic mesoporous shell for a cascade reaction.  Nanoscale,  7  (8): (3719-3725).  [PMID:25640736] [10.1039/C4NR06341D]
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