Cas no 53760-27-3 (N1-(4-Aminophenyl)benzene-1,4-diamine sulfate)
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate Chemical and Physical Properties
Names and Identifiers
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- N1-(4-Aminophenyl)benzene-1,4-diamine sulfate
- 4,4'-Diaminodiphenylamine Sulfate Hydrate
- 4,4'DIAMINODIPHENYLAMINE SULFATE
- N-(4-aminophenyl)benzene-1,4-diamine
- N-(4-Aminophenyl)-1,4-benzenediamine
- Bis(4-aminophenyl)amine Sulfate Hydrate
- 4,4'-Iminodianiline Sulfate Hydrate
- p,p'-Diaminodiphenylamine sulfate
- 4,4'-Diaminodiphenylamine Sulfate
- 02X5LJD26T
- AK126499
- C12H15N3O4S
- N4-(4-aminophenyl)benzene-1,4-diamine; sulfuric acid
- 4,4'-Iminodianiline Sulfate
- n-(4-aminophenyl)benzene-1,4-diamine sulfate(1:1)
- 4,4'-diaminodiphenylaminsulfat
- N-(4-Aminophenyl)benzene-1,4-diamine sulphate (1:1)
- Bis(4-aminophenyl)amine Sulfate
- 4,4-Diaminodiphe
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- MDL： MFCD00013113
- Inchi： 1S/C12H13N3.H2O4S/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12;1-5(2,3)4/h1-8,15H,13-14H2;(H2,1,2,3,4)
- InChI Key： OOZQLPDAELLDNY-UHFFFAOYSA-N
- SMILES： S(=O)(=O)(O[H])O[H].N([H])(C1C([H])=C([H])C(=C([H])C=1[H])N([H])[H])C1C([H])=C([H])C(=C([H])C=1[H])N([H])[H]
Computed Properties
- Exact Mass: 297.07800
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 5
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 20
- Rotatable Bond Count: 2
- Complexity: 241
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 147
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
Experimental Properties
- Color/Form: Yellow flake junction crystals.
- Melting Point: 300
- Boiling Point: No data available
- Flash Point: No data available
- PSA: 147.05000
- LogP: 4.25800
- Solubility: Soluble in ethanol and ether, insoluble in water.
- Vapor Pressure: No data available
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate Security Information
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Symbol:
- Prompt：warning
- Signal Word：warning
- Hazard Statement： H302+H312+H332-H315-H319
- Warning Statement： P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P501
- Hazardous Material transportation number：UN 2811 6.1/PG 3
- Safety Instruction： S24/25
- Safety Term：S24/25
- Storage Condition：Store at 4°C,-4At ℃Store…Better
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate 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%
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A602525-250mg |
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate |
53760-27-3 | 250mg |
$ 50.00 | 2022-06-08 | ||
| TRC | A602525-500mg |
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate |
53760-27-3 | 500mg |
$ 65.00 | 2022-06-08 | ||
| TRC | A602525-2.5g |
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate |
53760-27-3 | 2.5g |
$ 80.00 | 2022-06-08 | ||
| Alichem | A012001168-500g |
N-(4-Aminophenyl)-1,4-benzenediamine |
53760-27-3 | 97% | 500g |
$311.30 | 2023-09-01 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | D0041-500G |
4,4'-Diaminodiphenylamine Sulfate |
53760-27-3 | >97.0%(T) | 500g |
￥3625.00 | 2024-04-16 | |
| SHANG HAI YUAN YE Biotechnology Co., Ltd. | S19105-25g |
Fast Black B Salt |
53760-27-3 | 25g |
￥290.00 | 2021-09-02 | ||
| SHANG HAI YUAN YE Biotechnology Co., Ltd. | S19105-100g |
Fast Black B Salt |
53760-27-3 | 100g |
￥1050.00 | 2021-09-02 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | D858266-100g |
4,4'-Diaminodiphenylamine Sulfate Hydrate |
53760-27-3 | >97.0%(T) | 100g |
1,190.00 | 2021-05-17 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-SW928-1g |
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate |
53760-27-3 | 97% | 1g |
50.0CNY | 2021-08-06 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-SW928-25g |
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate |
53760-27-3 | 97% | 25g |
364.0CNY | 2021-08-06 |
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N1-(4-Aminophenyl)benzene-1,4-diamine sulfate Related Literature
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Philipp Traber,Stephan Kupfer,Stefanie Gr?fe,Isabelle Baussanne,Martine Demeunynck,Jean-Marie Mouesca,Serge Gambarelli,Vincent Artero,Murielle Chavarot-Kerlidou Chem. Sci., 2018,9, 4152-4159
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4. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
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Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
Additional information on N1-(4-Aminophenyl)benzene-1,4-diamine sulfate
Comprehensive Overview of N1-(4-Aminophenyl)benzene-1,4-diamine sulfate (CAS No. 53760-27-3)
N1-(4-Aminophenyl)benzene-1,4-diamine sulfate, identified by its CAS number 53760-27-3, is a specialized organic compound widely utilized in industrial and research applications. This compound belongs to the class of aromatic amines and is particularly valued for its role in dye synthesis, polymer chemistry, and material science. Its molecular structure, featuring both amino and phenyl groups, enables versatile reactivity, making it a critical intermediate in the production of high-performance materials.
In recent years, the demand for N1-(4-Aminophenyl)benzene-1,4-diamine sulfate has surged due to its applications in advanced material development. Researchers and manufacturers are increasingly exploring its potential in creating conductive polymers, which are pivotal in flexible electronics and energy storage solutions. The compound's ability to form stable complexes with metals also positions it as a candidate for catalysis and sensor technologies, aligning with the growing interest in sustainable and smart materials.
One of the most frequently searched questions regarding CAS No. 53760-27-3 revolves around its safety profile and handling precautions. While the compound is not classified as hazardous under standard regulations, proper laboratory practices, such as the use of personal protective equipment (PPE) and adequate ventilation, are recommended. This aligns with the broader industry trend toward safer chemical handling and green chemistry principles, which emphasize minimizing environmental and health risks.
The synthesis of N1-(4-Aminophenyl)benzene-1,4-diamine sulfate typically involves the sulfonation of 1,4-diaminobenzene derivatives, followed by purification steps to achieve high purity. This process is often optimized for scalability, catering to industrial demands. Recent advancements in synthetic methodologies have focused on reducing waste and improving yield, reflecting the global push toward more sustainable chemical production practices.
Another area of interest for CAS 53760-27-3 is its potential role in biomedical research. Preliminary studies suggest that derivatives of this compound may exhibit bioactive properties, sparking curiosity in its applications for diagnostic agents or therapeutic intermediates. However, further research is needed to validate these findings, highlighting the compound's untapped potential in life sciences.
From an SEO perspective, keywords such as "N1-(4-Aminophenyl)benzene-1,4-diamine sulfate uses," "53760-27-3 synthesis method," and "aromatic amine applications" are highly relevant. These terms reflect user intent and align with current trends in material science and chemical innovation. By addressing these queries, this article aims to provide a authoritative resource for professionals and enthusiasts alike.
In conclusion, N1-(4-Aminophenyl)benzene-1,4-diamine sulfate (CAS No. 53760-27-3) is a multifaceted compound with significant industrial and scientific relevance. Its applications span from advanced materials to potential biomedical uses, underscoring its importance in modern chemistry. As research continues to uncover new possibilities, this compound is poised to remain a key player in innovation-driven fields.
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