N-Methyl-4-nitroaniline - ≥98%(GC) , CAS No.100-15-2

CAS: 100-15-2 Cat. No.: M140177 Molecular Weight: 152.15 Beilstein Registry Number: 637920 EC Number: 202-823-2
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(GC)
Synonyms
N-METHYL-4-NITROBENZENAMINE | methyl(4-nitrophenyl)amine | 4-(Methylamino)nitrobenzene | N-(4-Nitrophenyl)-N-methylamine
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
M140177-5g
5
$9.90
25g
M140177-25g
3
$10.90
100g
M140177-100g
1
$35.90
250g
M140177-250g
2
$79.90
500g
M140177-500g
2
$131.90
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature Ships Normal 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

N-Methyl-4-nitroaniline (MNA) was used as an additive in the synthesis of insensitive explosives to reduce the melting temperature of energetic materials

Specifications

Synonyms
N-METHYL-4-NITROBENZENAMINE | methyl(4-nitrophenyl)amine | 4-(Methylamino)nitrobenzene | N-(4-Nitrophenyl)-N-methylamine
Specifications & Purity
≥98%(GC)
Storage
Room temperature
Shipped In
Normal
Purity
≥98%(GC)
Names and Identifiers
Pubchem Sid488180456
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180456
Canonical SmilesCNC1=CC=C(C=C1)[N+](=O)[O-]
IUPAC NameN-methyl-4-nitroaniline
InChIKeyXIFJZJPMHNUGRA-UHFFFAOYSA-N
INCHI1S/C7H8N2O2/c1-8-6-2-4-7(5-3-6)9(10)11/h2-5,8H,1H3
Isomeric SMILES CNC1=CC=C(C=C1)[N+](=O)[O-]
WGK Germany 3
UN Number 1661
Packing Group II
Molecular Weight 152.15
Beilstein 637920
Reaxy-Rn 637920
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=637920&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
SubclassNitrobenzenes
Intermediate Tree Nodes Not available
Direct ParentNitrobenzenes
Alternative Parents Phenylalkylamines  Nitroaromatic compounds  Aniline and substituted anilines  Secondary alkylarylamines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Nitrobenzene - Nitroaromatic compound - Phenylalkylamine - Aniline or substituted anilines - Secondary aliphatic/aromatic amine - C-nitro compound - Organic nitro compound - Organic oxoazanium - Secondary amine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Amine - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 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.

10 results found

Lot NumberCertificate TypeDateItem
B2217215Certificate of AnalysisDec 10, 2025 M140177
B2217219Certificate of AnalysisDec 10, 2025 M140177
B2217222Certificate of AnalysisDec 10, 2025 M140177
C2513526Certificate of AnalysisMar 03, 2025 M140177
C2513527Certificate of AnalysisMar 03, 2025 M140177
C2513528Certificate of AnalysisMar 03, 2025 M140177
D2607082Certificate of AnalysisMar 03, 2025 M140177
K1525058Certificate of AnalysisAug 04, 2023 M140177
B2217233Certificate of AnalysisJan 10, 2022 M140177
D2320128Certificate of AnalysisJan 10, 2022 M140177
Chemical and Physical Properties
Melt Point(°C)150.0-154.0℃
Molecular Weight152.150 g/mol
XLogP32.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass152.059 Da
Monoisotopic Mass152.059 Da
Topological Polar Surface Area57.900 Ų
Heavy Atom Count11
Formal Charge0
Complexity136.000
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
Citations of This Product
References
1. Ru Li, Xuan Zou, Pan Luan, Xiaokun Liu, Ning Wang, Qian Wang, Huashi Guan, Zhe Xu.  (2022)  Direct Determination of Enzymes in Dried Blood Spots by High-Performance Liquid Chromatography – Mass Spectrometry (HPLC-MS) for the Screening of Antithrombotic Agents.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2022.2053700]
2. 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]
3. 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,  (8): (3719-3725).  [PMID:25640736] [10.1039/C4NR06341D]
4. Wen-Jie Xu, Xue-Ning Cheng, Zhong-Xuan Han, Zhan-Jun Yang, Shu-Na Zhao, Hao Liu, Mi Li, Lin Jiang.  (2025)  Nanostructured electrospun nitrocellulose: Stabilization mechanisms and degradation kinetics of organic stabilizers.  FUEL,      [PMID:] [10.1016/j.fuel.2025.138094]
Solution Calculators
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