Cas no 623-09-6 (N-Methyl-1,4-phenylenediamine)
N-Methyl-1,4-phenylenediamine Chemical and Physical Properties
Names and Identifiers
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- N1-Methylbenzene-1,4-diamine
- N-methyl-p-phenylenediamine
- N-METHYL-1,4-BENZENEDIAMINE
- 4-Amino-N-Methylamine
- 4-Amino-N-methylaniline
- 4-methylaminoaniline
- N-methyl-1,4-phenylenediamine
- N-Methylbenzene-1,4-diamine
- p-methylaminoaniline
- 1,4-Benzenediamine, N-methyl-
- 623-09-6
- N4-methylbenzene-1,4-diamine
- FT-0655234
- 4-N-methylbenzene-1,4-diamine
- A833709
- DTXSID80211354
- W-105014
- AS-83594
- CS-0342994
- AKOS005350653
- MFCD00044895
- EN300-143017
- EINECS 210-770-1
- NS00035001
- SCHEMBL525926
- C78356
- methyl-p-phenylenediamine
- VVYWUQOTMZEJRJ-UHFFFAOYSA-N
- p-(Methylamino)aniline
- DTXCID80133845
- KRE4J89F9H
- 4-(methylamino)aniline
- 210-770-1
- N1-Methyl-1,4-benzenediamine
- 1-N-Methylbenzene-1,4-diamine
- N-Methyl-1,4-phenylenediamine
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- MDL: MFCD00044895
- Inchi: 1S/C7H10N2/c1-9-7-4-2-6(8)3-5-7/h2-5,9H,8H2,1H3
- InChI Key: VVYWUQOTMZEJRJ-UHFFFAOYSA-N
- SMILES: N(C)C1C=CC(=CC=1)N
Computed Properties
- Exact Mass: 122.08400
- Monoisotopic Mass: 122.084398
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 75
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.5
- Topological Polar Surface Area: 38
Experimental Properties
- Color/Form: Dark grey
- Density: 1.0343 (rough estimate)
- Melting Point: 36°C
- Boiling Point: 258.8 ℃ at 760 mmHg
- Flash Point: 127
- Refractive Index: 1.5103 (estimate)
- PSA: 38.05000
- LogP: 1.96470
- Vapor Pressure: 0.0±0.5 mmHg at 25°C
N-Methyl-1,4-phenylenediamine Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:Store in a cool, dry place. Keep container closed when not in use.
N-Methyl-1,4-phenylenediamine Customs Data
- HS CODE:2921590090
- Customs Data:
China Customs Code:
2921590090Overview:
2921590090. Other aromatic polyamines and derivatives and their salts. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
N-Methyl-1,4-phenylenediamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | M355745-5mg |
N-Methyl-1,4-phenylenediamine |
623-09-6 | 5mg |
$ 50.00 | 2022-06-03 | ||
| TRC | M355745-10mg |
N-Methyl-1,4-phenylenediamine |
623-09-6 | 10mg |
$ 65.00 | 2022-06-03 | ||
| TRC | M355745-50mg |
N-Methyl-1,4-phenylenediamine |
623-09-6 | 50mg |
$ 95.00 | 2022-06-03 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N15450-1g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 95% | 1g |
¥715.0 | 2024-07-19 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N15450-5g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 5g |
¥2259.0 | 2021-09-04 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N15450-25g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 25g |
¥6909.0 | 2021-09-04 | ||
| Alichem | A019088643-5g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 95% | 5g |
$206.78 | 2023-09-01 | |
| Alichem | A019088643-10g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 95% | 10g |
$323.01 | 2023-09-01 | |
| Alichem | A019088643-25g |
N1-Methylbenzene-1,4-diamine |
623-09-6 | 95% | 25g |
$653.66 | 2023-09-01 | |
| eNovation Chemicals LLC | D117157-5g |
4-Amino-N-methylaniline |
623-09-6 | 98% | 5g |
$305 | 2024-08-03 |
N-Methyl-1,4-phenylenediamine Suppliers
N-Methyl-1,4-phenylenediamine Related Literature
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Xiu-Li Wang,Xiao-Jun Li,Ru Sun,Yu-Jie Xu,Jian-Feng Ge Analyst 2016 141 2962
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2. 752. The Ehrlich–Sachs reaction. Part IID. M. W. Anderson,F. Bell J. Chem. Soc. 1959 3708
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3. Cytotoxic compounds. Part XVII. o-, m-, and p-(Bis-2-chloroethylamino)phenol, p-[N-(2-chloroethyl)methylamino]phenol, NN-bis-2-chloroethyl-p-phenylenediamine, and NN-bis-2-chloroethyl-N′-methyl-p-phenylenediamine as sources of biologically active carbamatesPeter D. Edwards,Duncan L. D. Foster,Leonard N. Owen,Michael J. Pringle J. Chem. Soc. Perkin Trans. 1 1973 2397
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4. Selective protection of polyamines: synthesis of model compounds and spermidine derivativesM. Lurdes S. Almeida,Leif Grehn,Ulf Ragnarsson J. Chem. Soc. Perkin Trans. 1 1988 1905
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Nathan Bossa,Alexis Wells Carpenter,Naresh Kumar,Charles-Fran?ois de Lannoy,Mark Wiesner Environ. Sci.: Nano 2017 4 1294
Additional information on N-Methyl-1,4-phenylenediamine
Recent Advances in the Application of N-Methyl-1,4-phenylenediamine (CAS 623-09-6) in Chemical Biology and Pharmaceutical Research
N-Methyl-1,4-phenylenediamine (CAS 623-09-6) is a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Recent studies have highlighted its significance in the development of novel therapeutic agents, particularly in the fields of oncology and neurodegenerative diseases. This research brief aims to summarize the latest findings on the applications and mechanisms of N-Methyl-1,4-phenylenediamine, providing insights into its potential as a versatile building block in drug discovery and chemical biology.
One of the most notable advancements involves the use of N-Methyl-1,4-phenylenediamine in the synthesis of polyaniline-based nanomaterials. These materials have shown promise in drug delivery systems due to their biocompatibility and conductive properties. A 2023 study published in Advanced Materials demonstrated that nanoparticles functionalized with N-Methyl-1,4-phenylenediamine exhibited enhanced targeting efficiency and controlled release of anticancer drugs, such as doxorubicin, in vitro and in vivo.
In addition to its role in drug delivery, N-Methyl-1,4-phenylenediamine has been investigated as a precursor for the development of novel enzyme inhibitors. Researchers have utilized its structural features to design compounds that selectively target monoamine oxidase (MAO) enzymes, which are implicated in neurodegenerative disorders like Parkinson's disease. A recent paper in Journal of Medicinal Chemistry reported the synthesis of a series of MAO-B inhibitors derived from N-Methyl-1,4-phenylenediamine, showing significant neuroprotective effects in preclinical models.
Furthermore, the compound's redox properties have been exploited in the development of biosensors. A 2024 study in Analytical Chemistry described a novel electrochemical sensor based on N-Methyl-1,4-phenylenediamine for the detection of reactive oxygen species (ROS) in biological samples. This sensor demonstrated high sensitivity and selectivity, making it a valuable tool for monitoring oxidative stress in disease states.
Despite these promising applications, challenges remain in optimizing the stability and bioavailability of N-Methyl-1,4-phenylenediamine-derived compounds. Ongoing research is focused on modifying its chemical structure to improve pharmacokinetic properties while retaining its therapeutic efficacy. Collaborative efforts between academic institutions and pharmaceutical companies are expected to accelerate the translation of these findings into clinical applications.
In conclusion, N-Methyl-1,4-phenylenediamine (CAS 623-09-6) continues to be a molecule of significant interest in chemical biology and pharmaceutical research. Its diverse applications—from drug delivery to enzyme inhibition and biosensing—highlight its potential as a multifunctional agent. Future studies should explore its utility in combination therapies and personalized medicine approaches, leveraging its unique chemical properties for targeted interventions.
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