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N,N-Dimethylbenzylamine
[CAS# 103-83-3]

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Complete supplier list of N,N-Dimethylbenzylamine
Identification
Classification Organic raw materials >> Amino compound >> Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts
Name N,N-Dimethylbenzylamine
Synonyms Benzyldimethylamine; BDMA
Molecular Structure CAS # 103-83-3, N,N-Dimethylbenzylamine, Benzyldimethylamine, BDMA
Molecular Formula C9H13N
Molecular Weight 135.21
CAS Registry Number 103-83-3
EC Number 203-149-1
SMILES CN(C)CC1=CC=CC=C1
Properties
Density 0.9
Melting point -75 ºC
Boiling point 183-184 ºC
Refractive index 1.5-1.502
Flash point 54 ºC
Water solubility 8 g/L (20 ºC)
Safety Data
Hazard Symbols symbol symbol symbol   GHS02;GHS05;GHS07 Danger    Details
Hazard Statements H226-H332-H312-H302-H314-H412    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P260-P261-P262-P264-P264+P265-P270-P271-P273-P280-P301+P316-P301+P317-P301+P330+P331-P302+P352-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P321-P330-P361+P364-P362+P364-P363-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.3H226
Skin corrosionSkin Corr.1BH314
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.3H331
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.3H311
Specific target organ toxicity - repeated exposureSTOT RE2H373
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Substances or mixtures corrosive to metalsMet. Corr.1H290
Acute toxicityAcute Tox.4H331
Transport Information UN 2619
SDS Available
up Discovory and Applicatios
N,N-Dimethylbenzylamine is an organic compound that belongs to the class of tertiary amines, featuring a benzyl group attached to a nitrogen atom substituted with two methyl groups. This compound has been widely studied due to its reactivity and versatility in both organic synthesis and industrial applications. Its structure makes it a useful catalyst and a reagent in various chemical reactions, particularly in the production of polymers and fine chemicals.

The discovery of N,N-Dimethylbenzylamine can be traced back to early investigations into amine derivatives and their role in catalysis and organic transformations. Tertiary amines like N,N-Dimethylbenzylamine are known for their nucleophilicity and basicity, properties that are crucial in numerous synthetic pathways. Early research demonstrated that the presence of both the benzyl group and the two methyl groups on the nitrogen atom significantly influenced the compound's reactivity, making it a suitable catalyst for several reactions. As a result, the compound became of interest in fields such as polymer chemistry and the manufacturing of pharmaceuticals and agrochemicals.

One of the primary applications of N,N-Dimethylbenzylamine is its use as a catalyst in polyurethane production. Polyurethanes are essential materials in a wide range of industries, including automotive, construction, and textiles. N,N-Dimethylbenzylamine acts as a catalyst in the reaction between isocyanates and polyols, facilitating the formation of polyurethane foams, coatings, and elastomers. Its ability to accelerate the reaction without undergoing significant side reactions makes it a valuable additive in the production process, ensuring high efficiency and quality in the final product.

In addition to its role in polymer chemistry, N,N-Dimethylbenzylamine is also utilized in organic synthesis. Its nucleophilic properties make it a suitable reagent in alkylation and acylation reactions, where it can promote the formation of carbon-nitrogen bonds. These reactions are important in the synthesis of pharmaceuticals, agrochemicals, and dyes, where the formation of amines and amides is a key step. The compound’s versatility as a base and nucleophile makes it a useful tool for chemists designing complex molecules.

Furthermore, N,N-Dimethylbenzylamine finds application in the production of quaternary ammonium compounds, which are used as disinfectants, fabric softeners, and surfactants. Quaternization of N,N-Dimethylbenzylamine leads to the formation of these cationic surfactants, which play a critical role in industrial and household cleaning products. Its role in the formation of such compounds underscores its importance in consumer goods and industrial processes.

Due to its widespread use in various industries, N,N-Dimethylbenzylamine continues to be an important compound for research and development. Its role in catalysis, polymer production, and synthetic chemistry ensures its ongoing relevance in both academic and industrial settings.
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