N-Methylaniline - ≥98% , CAS No.100-61-8

CAS: 100-61-8 Cat. No.: M109539 Molecular Weight: 107.15 Beilstein Registry Number: 741982 EC Number: 202-870-9
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
n-methylphenyl amine | N-metylaniline | N-Phenylmethylamine | RP10006 | EN300-19055 | NSC 3502 | SCHEMBL4454 | BIDD:GT0230 | N-Methylaniline, analytical standard | NSC3502 | NCGC00091265-01 | N-Methylaminobenzene | BP-31133 | J-523671 | AM10675 | Anilinom
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
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Size
Status
Price
Qty
50ml
M109539-50ml
1
$11.90
250ml
M109539-250ml
2
$23.90
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Why this grade

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

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Storage & shipping

Room temperature,Argon charged Ships 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 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

N-Methylaniline is a general reagent used:

• In the preparation of phosphoramidite ligands for the rhodium-catalyzed asymmetric hydroboration.

• As a formylating reagent in the C3-selective formylation of indoles.

• In the synthesis of a rhodol-based fluorescent probe, HKGreen-3, for sensing peroxynitrite.

• As a key starting material in the synthesis of AKT (protein kinase  inhibitor-IV.

Specifications

Synonyms
n-methylphenyl amine | N-metylaniline | N-Phenylmethylamine | RP10006 | EN300-19055 | NSC 3502 | SCHEMBL4454 | BIDD:GT0230 | N-Methylaniline, analytical standard | NSC3502 | NCGC00091265-01 | N-Methylaminobenzene | BP-31133 | J-523671 | AM10675 | Anilinom
Specifications & Purity
≥98%
Storage
Room temperature, Argon charged
Shipped In
FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504751375
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751375
Canonical SmilesCNC1=CC=CC=C1
IUPAC NameN-methylaniline
InChIKeyAFBPFSWMIHJQDM-UHFFFAOYSA-N
INCHI1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3
Isomeric SMILES CNC1=CC=CC=C1
WGK Germany 3
RTECS BY4550000
UN Number 2294
Packing Group III
Molecular Weight 107.15
Beilstein 741982
Reaxy-Rn 741982
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741982&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
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Aralkylamines
Direct ParentPhenylalkylamines
Alternative Parents Aniline and substituted anilines  Secondary alkylarylamines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalkylamine - Aniline or substituted anilines - Secondary aliphatic/aromatic amine - Benzenoid - Monocyclic benzene moiety - Secondary amine - Organopnictogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as phenylalkylamines. These are organic amines where the amine group is secondary and linked on one end to a phenyl group and on the other end, to an alkyl group.
External Descriptors a small molecule
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 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.

17 results found

Lot NumberCertificate TypeDateItem
I2213039Certificate of AnalysisJun 15, 2026 M109539
I2213037Certificate of AnalysisJun 15, 2026 M109539
I2212562Certificate of AnalysisJun 15, 2026 M109539
F2513127Certificate of AnalysisJun 27, 2025 M109539
E2126258Certificate of AnalysisMar 04, 2025 M109539
E2126157Certificate of AnalysisMar 04, 2025 M109539
G2418512Certificate of AnalysisApr 29, 2024 M109539
K2521054Certificate of AnalysisSep 02, 2022 M109539
J2429110Certificate of AnalysisSep 02, 2022 M109539
I2212564Certificate of AnalysisSep 02, 2022 M109539
I2212563Certificate of AnalysisSep 02, 2022 M109539
B2511076Certificate of AnalysisSep 02, 2022 M109539
E2527144Certificate of AnalysisMay 28, 2021 M109539
E2126259Certificate of AnalysisMay 28, 2021 M109539
A2508104Certificate of AnalysisMay 28, 2021 M109539
A2416067Certificate of AnalysisMay 28, 2021 M109539
C2419201Certificate of AnalysisMay 08, 2021 M109539

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Chemical and Physical Properties
SolubilityImmiscible with water.
SensitivityLight & Air sensitive
Refractive Index1.5694-1.5714
Flash Point(°F)86℃
Flash Point(°C)86℃
Boil Point(°C)195°C
Melt Point(°C)-57°C
Molecular Weight107.150 g/mol
XLogP31.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass107.073 Da
Monoisotopic Mass107.073 Da
Topological Polar Surface Area12.000 Ų
Heavy Atom Count8
Formal Charge0
Complexity55.400
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
Citations of This Product
References
1. Meili Ding, Pan Ma, Yang Wang, Ying Zhang, Jun Liu, Jianfeng Yao.  (2023)  Hierarchically porous bimetallic oxide derived from a metal-organic framework for the promotion of catalytic CO2 chemical fixation.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2023.111118]
2. Tao Wang, Jie Li, Hanwen Yan, Guoliang Zhang, Shifeng Li.  (2023)  Mechanism and Kinetic Study on Synthesis of Methacrolein Catalyzed by Amine/Acid.  Catalysts,  13  (5): (799).  [PMID:] [10.3390/catal13050799]
3. Zhengyu Wang, Yufeng Hu, Zhiduo Ding, Hao Zhou, Jianye Zhang, Jingjing Zhan, Minghuo Wu.  (2023)  Determination of Organic Nitrogen Compounds in Gasoline by Water-Assisted Dispersive Solid-Phase Extraction (DSPE) and High-Performance Liquid Chromatography-High-Resolution Mass Spectrometry (HPLC-HRMS).  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2022.2101059]
4. Li Li, Feng Xu, Ge Sun, Mingrui Sun, Shoushi Jia, Hongmei Li, Tao Xu, Honglian Zhang, Yan Wang, Yue Guo, Taohua Liu.  (2021)  Identification of N-methylaniline based on azo coupling reaction by combining TLC with SERRS.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:33524815] [10.1016/j.saa.2021.119490]
5. Chaoyue Xiong, Guodong Xue, Lijun Mao, Lianghong Gu, Chao He, Yonghao Zheng, Dongsheng Wang.  (2021)  Carbon Spacer Strategy: Control the Photoswitching Behavior of Donor–Acceptor Stenhouse Adducts.  LANGMUIR,      [PMID:33406356] [10.1021/acs.langmuir.0c03133]
6. Chuanbo Hu, Ying Li, Tingzhen Li, Yongquan Qing, Jianting Tang, Huawei Yin, Lei Hu, Lei Zhang, Yongsheng Xie, Kangning Ren.  (2019)  Fabrication of poly(N-methylaniline)/SiC-ZnO bilayer coatings onto the carbon steel substrate and studies on its anticorrosion properties.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2019.124176]
7. Zhang Yinchenxi, Duan Yixiang.  (2019)  A double-functionalized polymeric ionic liquid used as solid-phase microextraction coating for efficient aromatic amine extraction and detection with gas chromatography–mass spectrometry.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  411  (10): (2209-2221).  [PMID:30879115] [10.1007/s00216-019-01664-x]
8. Wenfeng Zhao, Xiaoping Chi, Hu Li, Jian He, Jingxuan Long, Yufei Xu, Song Yang.  (2018)  Eco-friendly acetylcholine-carboxylate bio-ionic liquids for controllable N-methylation and N-formylation using ambient CO2 at low temperatures.  GREEN CHEMISTRY,  21  (3): (567-577).  [PMID:] [10.1039/C8GC03549K]
9. Yingzhuang Chen, Keyi Wang, Huihui Yang, Yixuan Liu, Shouzhuo Yao, Bo Chen, Lihua Nie, Guangming Xu.  (2012)  Synthesis of sulfo/vinyl biphasic silica hybrid monolithic capillary column and its application to on-column preconcentration for capillary electrochromatography.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:22410157] [10.1016/j.chroma.2012.01.024]
10. Min-Fu Wu, Nuo Xu, Sha Li, Yi-Lan Huang, Min-Hua Wu, Jia-Dong Li, Ri-Sheng Chen, Wen-Ming Xiong, Yong-Jun Li, Hong-Tao Lei, Xin-An Huang, Zhen-Lin Xu.  (2024)  A hapten design strategy to enhance the selectivity of monoclonal antibodies against malachite green.  Frontiers in Sustainable Food Systems,      [PMID:] [10.3389/fsufs.2024.1490750]
11. Jianxiang Wu, Yuxin Chen, Wei Du, Yaming Hao, Shaoyan Wang, Ran Wang, Shuangshuang Cha, Xuejing Yang, Chang Yan, Cheng Lian, Honglai Liu, Ming Gong.  (2025)  Concentrated Zwitterion Interfaces for Selective Promotion of Electrochemical Hydroxide Oxidation.  Journal of the American Chemical Society,      [PMID:40866311] [10.1021/jacs.5c08459]
12. Youhong Ai, Faqiong Zhao, Baizhao Zeng.  (2015)  Novel proton-type ionic liquid doped polyaniline for the headspace solid-phase microextraction of amines.  ANALYTICA CHIMICA ACTA,      [PMID:26092338] [10.1016/j.aca.2015.04.028]
13. Linlin Li, Jiang Zhao, Qingmei Ge, Yin-Hui Huang, Hang Cong, Wenfeng Zhao.  (2026)  A bioinspired chitosan-polymer facilitated CO2 utilization under mild reaction conditions.  BIOMASS & BIOENERGY,      [PMID:] [10.1016/j.biombioe.2026.109082]
14. Meilin Zhao, Zhihua Huang, Shuoyang Sun, Quan Gan, Shuang Wu, Xiqi Hu, Delei Xu, Pedro Laborda, Bao Tang, Lingtian Wu.  (2026)  Bacillus velezensis LT-22 Volatiles for the Biocontrol of Phytophthora capsici: Antifungal Action and Underlying Mechanisms.  Foods,  15  (4): (753).  [PMID:41750945] [10.3390/foods15040753]
15. Yixin Huang, Yihui Zhang, Mengzhe Zhao, Shuwen Yan, Weihua Song.  (2026)  Reaction of the Peroxyacetyl Radical with Dissolved Organic Matter: Kinetics, Mechanism, and Impacts on Contaminant Degradation.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:41715887] [10.1021/acs.est.5c16661]
16. Ge-liang Xie, Yu Luo, Kai-cheng Xia, Sheng-ren Li, Lujiang Xu, Zhen Fang.  (2026)  Elucidating functional group governance for catalytic synthesis of bio-based aromatic amines.  BIOMASS & BIOENERGY,      [PMID:] [10.1016/j.biombioe.2026.109198]
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