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2,2'-[(4-Methylphenyl)imino]bisethanol
[CAS# 3077-12-1]

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Complete supplier list of 2,2'-[(4-Methylphenyl)imino]bisethanol
Identification
Classification Organic raw materials >> Amino compound >> Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts
Name 2,2'-[(4-Methylphenyl)imino]bisethanol
Synonyms N,N-Dihydroxyethyl-p-toluidine
Molecular Structure CAS # 3077-12-1, 2,2'-[(4-Methylphenyl)imino]bisethanol, N,N-Dihydroxyethyl-p-toluidine
Protein Sequence G
Molecular Formula C11H17NO2
Molecular Weight 195.26
CAS Registry Number 3077-12-1
EC Number 221-359-1
SMILES CC1=CC=C(C=C1)N(CCO)CCO
Properties
Density 1.1±0.1 g/cm3, Calc.*
Melting point 49-53 ºC
Index of Refraction 1.587, Calc.*
Boiling Point 339.0±0.0 ºC (760 mmHg), Calc.*, 338-340 ºC
Flash Point 208.9±23.8 ºC, Calc.*, 113 ºC
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H302-H315-H317-H318-H319-H335-H412    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P272-P273-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P330-P332+P317-P333+P317-P337+P317-P362+P364-P403+P233-P405-    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Skin sensitizationSkin Sens.1H317
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Skin sensitizationSkin Sens.1BH317
SDS Available
up Discovory and Applicatios
2,2'-[(4-Methylphenyl)imino]bisethanol, commonly referred to as a bis(phenyl) imine derivative, is an organic compound characterized by the presence of an imine functional group connecting two ethanol units to a 4-methylphenyl moiety. The discovery of this compound is rooted in the ongoing exploration of imines and their derivatives, which have gained prominence in organic chemistry for their reactivity and potential applications in various fields, including catalysis, materials science, and pharmaceuticals.

The synthesis of 2,2'-[(4-Methylphenyl)imino]bisethanol typically involves the condensation reaction between 4-methylphenyl amine and an appropriate aldehyde, such as ethyl aldehyde, in the presence of an acid catalyst. This reaction leads to the formation of the imine linkage and the subsequent addition of ethanol units, resulting in the desired compound. The structural attributes of 2,2'-[(4-Methylphenyl)imino]bisethanol contribute to its unique chemical behavior, making it an important subject of study.

One of the notable applications of 2,2'-[(4-Methylphenyl)imino]bisethanol lies in the field of catalysis. Compounds featuring imine linkages have demonstrated significant potential as ligands in coordination chemistry, often enhancing the activity of metal complexes. In this context, 2,2'-[(4-Methylphenyl)imino]bisethanol can act as a bidentate ligand, coordinating with transition metals to form stable complexes. These metal-ligand complexes have been utilized in various catalytic processes, including oxidation reactions, polymerization, and cross-coupling reactions, thereby playing a crucial role in the development of sustainable chemical processes.

In addition to its catalytic applications, 2,2'-[(4-Methylphenyl)imino]bisethanol is also of interest in materials science. The compound's ability to form hydrogen bonds and its structural rigidity make it suitable for incorporation into polymer matrices, contributing to the development of high-performance materials with enhanced mechanical properties. Research has shown that the addition of imine-based compounds can improve thermal stability and reduce brittleness in polymer systems, making them more suitable for demanding applications in electronics and aerospace.

Furthermore, 2,2'-[(4-Methylphenyl)imino]bisethanol has potential applications in the pharmaceutical industry. The imine functional group is a common motif in drug design, as it can influence the pharmacological properties of compounds. Studies have indicated that imine derivatives can exhibit a range of biological activities, including antimicrobial and anticancer properties. As such, 2,2'-[(4-Methylphenyl)imino]bisethanol may serve as a valuable building block for the synthesis of novel therapeutic agents.

Despite its promising applications, the use of 2,2'-[(4-Methylphenyl)imino]bisethanol necessitates careful consideration of safety and regulatory aspects. As with many organic compounds, proper handling and adherence to safety guidelines are essential to minimize potential health risks. Regulatory agencies evaluate the safety profiles of chemical substances to ensure that they are used responsibly and in accordance with established guidelines.

In conclusion, 2,2'-[(4-Methylphenyl)imino]bisethanol is a versatile organic compound with diverse applications in catalysis, materials science, and pharmaceuticals. Its unique chemical structure enables it to participate in various chemical processes, enhancing the performance of materials and contributing to the development of new therapeutic agents. As research continues to explore the potential of imine derivatives, 2,2'-[(4-Methylphenyl)imino]bisethanol is expected to play an increasingly significant role in advancing multiple scientific fields.
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