Cas no 53708-21-7 (2-(dodecyloxy)pyridine)
2-(dodecyloxy)pyridine Chemical and Physical Properties
Names and Identifiers
-
- 2-(dodecyloxy)pyridine
- 4-dodecyloxybenzene boronic acid
- 4-dodecyloxyphenylboronic acid
- 4-Dodecyloxypyridin
- 4-dodecyloxy-pyridine
- NSC 74508
- NS00037037
- DB-052386
- DTXSID00220524
- NSC74508
- UNII-18P44R839H
- 53708-21-7
- EINECS 274-541-8
- AKOS024332456
- 2-dodecyloxypyridine
- 18P44R839H
- 2-dodecoxypyridine
- SCHEMBL4885285
- 70289-09-7
- NSC-74508
- PQKOSPVOQVXHCT-UHFFFAOYSA-N
- Pyridine, 2-(dodecyloxy)-
-
- Inchi： 1S/C17H29NO/c1-2-3-4-5-6-7-8-9-10-13-16-19-17-14-11-12-15-18-17/h11-12,14-15H,2-10,13,16H2,1H3
- InChI Key： PQKOSPVOQVXHCT-UHFFFAOYSA-N
- SMILES： O(C1C=CC=CN=1)CCCCCCCCCCCC
Computed Properties
- Exact Mass: 263.22500
- Monoisotopic Mass: 263.224914549g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 19
- Rotatable Bond Count: 12
- Complexity: 184
- 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: 7.1
- Topological Polar Surface Area: 22.1?2
Experimental Properties
- Density: 0.9±0.1 g/cm3
- Melting Point: NA
- Boiling Point: 349.8±15.0 °C at 760 mmHg
- PSA: 22.12000
- LogP: 5.38130
- Vapor Pressure: 0.0±0.7 mmHg at 25°C
2-(dodecyloxy)pyridine Security Information
- Signal Word：warning
- Hazard Statement： H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement： P264+P280+P305+P351+P338+P337+P313
- Safety Instruction： H303+H313+H333
- Storage Condition：storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
2-(dodecyloxy)pyridine Customs Data
- HS CODE：2933399090
- Customs Data：
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
2-(dodecyloxy)pyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D535838-250mg |
2-(Dodecyloxy)Pyridine |
53708-21-7 | 250mg |
$ 70.00 | 2022-06-05 | ||
| TRC | D535838-500mg |
2-(Dodecyloxy)Pyridine |
53708-21-7 | 500mg |
$ 95.00 | 2022-06-05 | ||
| TRC | D535838-2.5g |
2-(Dodecyloxy)Pyridine |
53708-21-7 | 2.5g |
$ 340.00 | 2022-06-05 |
2-(dodecyloxy)pyridine Related Literature
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M. T. Colomer,S. Díaz-Moreno,A. Tamayo,A. L. Ortiz J. Mater. Chem. C, 2018,6, 12643-12651
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
Additional information on 2-(dodecyloxy)pyridine
Introduction to 2-(dodecyloxy)pyridine (CAS No. 53708-21-7)
2-(dodecyloxy)pyridine, also known by its CAS number 53708-21-7, is a compound that has garnered significant attention in various scientific and industrial applications. This compound belongs to the class of pyridine derivatives, which are widely studied for their unique chemical properties and potential uses in fields such as materials science, pharmacology, and environmental chemistry.
The molecular structure of 2-(dodecyloxy)pyridine consists of a pyridine ring with a dodecyloxy group attached at the second position. The pyridine ring is an aromatic six-membered ring containing one nitrogen atom, while the dodecyloxy group introduces a long hydrocarbon chain, making the compound amphiphilic in nature. This amphiphilicity is a key feature that contributes to its versatile applications.
Recent studies have highlighted the potential of 2-(dodecyloxy)pyridine in enhancing the performance of various materials, particularly in the realm of polymer science. Researchers have explored its ability to act as a compatibilizer, improving the interfacial adhesion between different polymer phases. This property is particularly valuable in the development of high-performance composites and blends, where achieving optimal interfacial interactions is crucial for mechanical and thermal stability.
In addition to its role in materials science, 2-(dodecyloxy)pyridine has shown promise in drug delivery systems. Its amphiphilic nature allows it to form self-assembled structures, such as micelles or vesicles, which can encapsulate hydrophobic drugs. These nanostructures have been investigated for their ability to improve drug solubility, stability, and targeted delivery, making them a potential candidate for advanced pharmaceutical formulations.
The synthesis of 2-(dodecyloxy)pyridine typically involves nucleophilic substitution reactions or coupling reactions, depending on the desired purity and scale of production. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly synthesis routes, reducing the overall cost and ecological footprint associated with its production.
Moreover, 2-(dodecyloxy)pyridine has been studied for its applications in environmental remediation. Its ability to adsorb and remove heavy metal ions from aqueous solutions has been explored in various experimental setups. The compound's hydrophobic tail facilitates interaction with organic pollutants, while its polar pyridine ring can coordinate with metal ions through ligand exchange mechanisms. This dual functionality makes it a potential candidate for developing cost-effective water treatment technologies.
In terms of safety and handling, 2-(dodecyloxy)pyridine is generally considered non-hazardous under normal conditions; however, appropriate precautions should be taken during synthesis and handling to ensure compliance with occupational safety standards.
In conclusion, 2-(dodecyloxy)pyridine, with its unique chemical properties and versatile applications across multiple disciplines, continues to be an area of active research and development. As new insights into its structure-property relationships emerge, it holds the potential to contribute significantly to advancing technologies in materials science, pharmacology, and environmental chemistry.
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