p-Anisidine - ≥95% , CAS No.104-94-9

CAS: 104-94-9 Cat. No.: A615348 分子式: C7H9NO 分子量: 123.15 Beilstein Registry Number: 471556 EC番号: 203-254-2
注文可能
GRADE & PURITY ≥95%
Synonyms
InChI=1/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H | STR00220 | para-methoxy aniline | p-Methoxyaniline | p-methoxy-aniline | 4-Methoxyaniline--d4 | EINECS 203-254-2 | AC-565 | FT-0693135 | NSC7921 | NSC-7921 | UNII-575917SNR4 | 4-(methyloxy)aniline | 4meth
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice,FedEx DG Service
★
Size
USA
ドイツ (EU)*
Price
Qty
25g
A615348-25g
受注生産 · 8~12週間
$9.90
100g
A615348-100g
1 在庫あり
—
$15.90
250g
A615348-250g
3 在庫あり
—
$29.90
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged 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 33 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

An aromatic compound used in the detection of aldehydes or ketones in oils.

Specifications

同義語
InChI=1/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H | STR00220 | para-methoxy aniline | p-Methoxyaniline | p-methoxy-aniline | 4-Methoxyaniline--d4 | EINECS 203-254-2 | AC-565 | FT-0693135 | NSC7921 | NSC-7921 | UNII-575917SNR4 | 4-(methyloxy)aniline | 4meth
仕様と純度
≥95%
保管条件
Store at 2-8°C,Protected from light,Argon charged
入荷
Wet ice,FedEx DG Service
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
純度
≥95%
名前と識別子
パブケム・シド
カノニカル・スマイル
COC1=CC=C(C=C1)N
IUPAC Name
4-methoxyaniline
InChIKey
BHAAPTBBJKJZER-UHFFFAOYSA-N
INCHI
1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
異性体SMILES
COC1=CC=C(C=C1)N
WGKドイツ
2
RTECS
BZ5450000
UN番号
2431
包装グループ
III
分子量
123.15
Beilstein
471556
Reaxy-Rn
471556
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=471556&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
分類Phenol 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
説明This 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 methoxybenzene
3 D構造
インタラクティブ化学構造モデル





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作用メカニズム
証明書(CoA、COO、BSE/TSEと分析図)
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.

19 results found

Lot NumberCertificate Type日付商品
F2615167Certificate of AnalysisJun 26, 2026 A615348
F2615168Certificate of AnalysisJun 26, 2026 A615348
F2615170Certificate of AnalysisJun 26, 2026 A615348
F2615171Certificate of AnalysisJun 26, 2026 A615348
F2615176Certificate of AnalysisJun 26, 2026 A615348
D2623776Certificate of AnalysisApr 27, 2026 A615348
G2416172Certificate of AnalysisApr 29, 2024 A615348
G2416173Certificate of AnalysisApr 29, 2024 A615348
I2509023Certificate of AnalysisAug 31, 2023 A615348
A2612031Certificate of AnalysisAug 31, 2023 A615348
I2412021Certificate of AnalysisAug 31, 2023 A615348
H2328139Certificate of AnalysisAug 31, 2023 A615348
H2328138Certificate of AnalysisAug 31, 2023 A615348
H2328137Certificate of AnalysisAug 31, 2023 A615348
H2328136Certificate of AnalysisAug 31, 2023 A615348
H2328135Certificate of AnalysisAug 31, 2023 A615348
F2509030Certificate of AnalysisAug 31, 2023 A615348
E2507054Certificate of AnalysisAug 31, 2023 A615348
D2623775Certificate of AnalysisAug 31, 2023 A615348
化学的性質と物理的性質
溶解度Soluble in acetone, benzene, ether and ethanol. Insoluble in water.
感度Light sensitive;Air & Moisture Sensitive;Heat sensitive
引火点(°F)251.6 °F
引火点(°C)122℃
沸点(°C)240-243°C
融点(°C)56-59°C
分子量123.150 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
Complexity77.000
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
よくある質問と記事
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
One-Pot Deaminative Cyanation of Arylamines Mediated by Nitrate Reduction: The ORT Pathway and Kinetic Matching of Tandem Reaction Steps
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
ソリューション計算機
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