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N,N-Dimethylbenzylamine is suggested that the products derive from an intracomplex hydrogen atom transfer in a reversibly formed charge-transfer complex.
N,N-Dimethylbenzylamine a colorless to light yellow liquid with an aromatic odor.
N,N-Dimethylbenzylamine is used in the manufacture of adhesives and other chemicals.
CAS Number: 103-83-3
Molecular Formula: C9H13N
Molecular Weight: 135.21
EINECS Number: 203-149-1
Synonyms: N,N-Dimethylbenzylamine , 103-83-3, N,N-Dimethylbenzylamine , N,N-Dimethylbenzylamine , N,N-dimethyl-1-phenylmethanamine, Dimethylbenzylamine, BDMA, Benzenemethanamine, N,N-dimethyl-, Benzyl-N,N-dimethylamine, N-(Phenylmethyl)dimethylamine, N,N-Dimethylbenzenemethanamine, Araldite accelerator 062, N,N-Dimethyl-N-benzylamine, N-Benzyl-N,N-dimethylamine, Benzylamine, N,N-dimethyl-, Sumine 2015, N,N'-Dimethylbenzylamine, NSC 5342, Benzyl-dimethyl-amine, TYP7AXQ1YJ, DTXSID8021854, NSC-5342, NCGC00090991-02, 28262-13-7, DTXCID801854, CAS-103-83-3, CCRIS 6693, UNII-TYP7AXQ1YJ, EINECS 203-149-1, UN2619, Benzenemethanamine, dimethyl-, AI3-26794, Benzenemethamine, N,N-dimethyl-, Dabco BDMA, N,N-dimethyl-1-phenyl-methanamine, benzyldimethyl-amine, dimethylbenzyl amine, n-dimethylbenzylamine, dimethyl benzyl amine, N,N-Dmethylbenzylamne, N-benzyl dimethylamine, Benzylamine,N-dimethyl-, N,N,-dimethylbenzylamine, N,N-dimethyl benzylamine, N,N-dimethyl-benzylamine, N, N-Dimethylbenzylamine, N,N-dimethyl benzyl amine, Benzenemethanamine,dimethyl-, EC 203-149-1, dimethyl (phenylmethyl)amine, SCHEMBL15900, MLS002222342, CHEMBL45591, N,N-Dimethyl(phenyl)methanamine, NSC5342, N,N-Dimethylbenzylamine , >=99%, N,N-Dimethyl(phenyl)methanamine #, WLN: 1N1 & 1R, Tox21_113457, Tox21_200719, MFCD00008329, AKOS000120578, UN 2619, NCGC00090991-01, NCGC00090991-03, NCGC00258273-01, AC-10211, LS-13652, SMR001307284, N,N-Dimethylbenzylamine (N,N-Dimethylbenzylamine ), N,N-Dimethylbenzylamine [UN2619] [Corrosive], D0688, FT-0657620, NS00008694, EN300-16212, N,?N-?Dimethylbenzylamine(N,N-Dimethylbenzylamine ), Q424966, J-001043, J-523270, InChI=1/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H, N,N-Dimethylbenzylamine , for protein sequence analysis, >=99.5% (GC).
N,N-Dimethylbenzylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide.
N,N-Dimethylbenzylamine acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.
N,N-Dimethylbenzylamine is an intermediate for organic synthesis, such as synthesis of quaternary ammonium salt, also used in dehydrogenation catalyst, preservative, acid neutralizer, etc.
N,N-Dimethylbenzylamine appears as a colorless to light yellow liquid with an aromatic odor with the formula C9H13N .
Mainly Used in the manufacture of adhesives and other chemicals.
N,N-Dimethylbenzylamine , also known as N-benzyl-n,n-dimethylamine nitrate or benzyl-dimethyl-amine, is a member of the class of compounds known as phenylmethylamines.
N,N-Dimethylbenzylamine s are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
N,N-Dimethylbenzylamine is slightly soluble (in water) and a very strong basic compound (based on its pKa).
N,N-Dimethylbenzylamine can be found in tea, which makes N,N-Dimethylbenzylamine a potential biomarker for the consumption of this food product.
N,N-Dimethylbenzylamine , also known as N,N-Dimethylbenzylamine, is a chemical compound with the molecular formula C9H13N.
N,N-Dimethylbenzylamine is classified as a tertiary amine due to its nitrogen atom bonded to three carbon groups.
The chemical structure of N,N-Dimethylbenzylamine consists of a benzene ring attached to a methyl group and a dimethylamine group.
N,N-Dimethylbenzylamine is typically soluble in organic solvents like ethanol and ether but may have limited solubility in water.
N,N-Dimethylbenzylamine can be used to synthesize quaternary ammonium salts by reacting it with alkyl halides.
These quaternary ammonium salts may find applications as phase transfer catalysts or antimicrobial agents.
The dimethylamine group in N,N-Dimethylbenzylamine can undergo reactions with various electrophiles, allowing it to participate in a range of organic synthesis processes.
In certain applications, N,N-Dimethylbenzylamine may be employed as a corrosion inhibitor, helping to prevent or reduce corrosion in metal surfaces.
N,N-Dimethylbenzylamine is utilized in laboratory settings for its catalytic properties and as a reactant in organic synthesis.
N,N-Dimethylbenzylamine may be used in industrial processes where its catalytic or intermediate properties are beneficial.
N,N-Dimethylbenzylamine can be used in analytical chemistry, particularly for protein sequence analysis.
Proper disposal practices should be followed to minimize environmental impact, and it's important to handle and dispose of the compound in accordance with regulations.
Users and handlers of N,N-Dimethylbenzylamine should refer to the Safety Data Sheet (SDS) provided by the manufacturer or supplier for specific safety guidelines, handling procedures, and emergency measures.
N,N-Dimethylbenzylamine , the benzyl chloride was added dropwise over a two-hour period to the amine at a rate sufficient to maintain the temperature below 40°C.
Stirring was continued at room temperature for an additional hour to insure completion of the reaction denoted by the equation below.
Thereafter the reaction mixture was cooled in a separatory funnel while standing in a refrigerator maintained at 5° C.
The upper oily layer, weighing 111.5g, was removed and steam distilled until no further oleaginous component was observed in the distillate as it came over.
N,N-Dimethylbenzylamine is a colorless liquid.
N,N-Dimethylbenzylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.
N,N-Dimethylbenzylamine is commonly used as a reagent in organic synthesis and also serves as a catalyst in the synthesis of polyurethane foams and epoxy resins.
N,N-Dimethylbenzylamine can also be prepared by reacting benzyl chloride with dimethylamine .
N,N-Dimethylbenzylamine is a flammable, low-volatility, colorless liquid with a foul, amine-like odor that is poorly soluble in water.
N,N-Dimethylbenzylamine is aqueous solution has an alkaline reaction.
Slightly less dense than water and slightly soluble in water.
Corrosive to skin, eyes and mucous membranes.
The crude distillate was found to contain 103.5g of N,N-Dimethylbenzylamine (76.1% of theory), 3.3g of N,N-Dimethylbenzylamine and no quaternary salts.
The N,N-Dimethylbenzylamine was distilled off below 29°C under atmospheric pressure from the N,N-Dimethylbenzylamine (bp 82°C/18mmHg).
N,N-Dimethylbenzylamine neutralizes acids on exothermic reactions to form salts plus water.
May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.
Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. May attack some plastics.
N,N-Dimethylbenzylamine can be obtained by reacting benzylamine with methanol in the presence of hydrogen chloride as a catalyst.
Slightly toxic by ingestion, skin absorption and inhalation.
N,N-Dimethylbenzylamine appears as a colorless to light yellow liquid with an aromatic odor.
N,N-Dimethylbenzylamine is used in the manufacture of adhesives; dehydrohalogenating catalyst; corrosion inhibitor; acid neutralizer; potting compounds; cellulose modifier and quaternary ammonium compounds.
N,N-Dimethylbenzylamine has a viscosity of 3 mPa s at 20 °C.
N,N-Dimethylbenzylamine is the organic compound with the formula C6H5CH2N(CH3)2.
The molecule consists of a benzyl group, C6H5CH2, attached to a dimethylamino functional group.
N,N-Dimethylbenzylamine reacts with Os3(CO)12 to form triosmium clusters.
Anodic oxidation of N,N-Dimethylbenzylamine has been studied in methanol-tetra-n-butylammonium fluoroborate and in methanol-potassium hydroxide.
A product study of the reaction of N,N-Dimethylbenzylamine with thermally and photochemically generated 1O2 in MeCN was carried out.
N,N-Dimethylbenzylamine and N-benzyl-N-methylformamide are the reaction products, oxygenation representing ca. 9% of the overall quenching of 1O2 by 1.
The temperature effect and the intermolecular and intramolecular kinetic deuterium isotope effects were also determined.
N,N-Dimethylbenzylamine undergoes directed ortho metalation with butyl lithium.
N,N-Dimethylbenzylamine reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts.
N,N-Dimethylbenzylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.
Melting point: -75 °C
Boiling point: 183-184 °C765 mm Hg(lit.)
Density: 0.9 g/mL at 25 °C(lit.)
vapor pressure: 2.4 hPa (20 °C)
refractive index: n20/D 1.501(lit.)
Flash point: 130 °F
storage temp.: Store below +30°C.
solubility: water: soluble
pka: pK1:9.02(+1) (25°C)
form: Liquid
color: Clear colorless to light yellow
PH: 10 (10g/l, H2O, 20℃)(saturated solution)
Odor: strong fish odor
explosive limit 0.9-6.3%(V)
Water Solubility: 8 g/L (20 ºC)
Sensitive: Air Sensitive
BRN: 1099620
Stability: Stable. Incompatible with strong acids, strong oxidizing agents.
LogP: 1.98 at 25℃
N,N-Dimethylbenzylamine may be involved in certain polymerization reactions, contributing to the synthesis of polymers with specific properties.
Some quaternary ammonium compounds derived from N,N-Dimethylbenzylamine have antimicrobial properties, which can be beneficial in formulations like disinfectants and sanitizers.
In certain industrial applications, N,N-Dimethylbenzylamine can act as a corrosion inhibitor, helping to protect metal surfaces from corrosion.
N,N-Dimethylbenzylamine is involvement in various reactions and its role as an intermediate in organic synthesis contribute to its significance in the preparation of diverse chemical compounds.
N,N-Dimethylbenzylamine is utilized in protein sequence analysis, showcasing its importance in biochemical and analytical applications.
The compound may find applications in research and development, contributing to the synthesis of novel materials and compounds.
Proper handling and storage practices, as outlined in the Safety Data Sheet (SDS), are crucial to ensure the safety of individuals working with N,N-Dimethylbenzylamine .
Users should comply with local regulations and guidelines regarding the handling, storage, and disposal of N,N-Dimethylbenzylamine .
N,N-Dimethylbenzylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide.
N,N-Dimethylbenzylamine acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.
N,N-Dimethylbenzylamine undergoes directed ortho metalation with butyl lithium.
N,N-Dimethylbenzylamine reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts.
N,N-Dimethylbenzylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.
N,N-Dimethylbenzylamine is a slightly toxic, flammable, colorless to light yellow liquid organic compound with an aromatic odor.
N,N-Dimethylbenzylamine is used in the manufacture of adhesives and other chemicals.
N,N-Dimethylbenzylamine may exhibit hygroscopic properties, meaning it has the ability to absorb moisture from the surrounding environment.
N,N-Dimethylbenzylamine can be incorporated into resin formulations, contributing to the curing process and modifying the properties of the final cured resin.
In polymer chemistry, N,N-Dimethylbenzylamine may serve as an additive to modify the properties of certain polymers.
N,N-Dimethylbenzylamine can be used in the formulation of adhesives, influencing the curing and adhesive properties of the final product.
Some derivatives of N,N-Dimethylbenzylamine may find applications in pharmaceuticals, either as intermediates or as components in drug formulations.
N,N-Dimethylbenzylamine may act as a complexing agent in certain chemical processes, forming stable complexes with metal ions.
N,N-Dimethylbenzylamine is used as a chemical reagent in various laboratory procedures, including organic synthesis and analytical chemistry.
The compound's chemical structure and properties make it compatible with a range of other compounds, allowing for diverse applications in different formulations.
Users should follow proper handling precautions, including the use of appropriate personal protective equipment, when working with N,N-Dimethylbenzylamine .
Compliance with local, regional, and international regulations is essential when using N,N-Dimethylbenzylamine , and users should be aware of any restrictions or guidelines.
N,N-Dimethylbenzylamine is often available in different grades, including technical grade, and the specific grade may depend on the intended application.
Like many amines, N,N-Dimethylbenzylamine may have an amine-like odor, and exposure to high concentrations should be avoided.
Adequate ventilation and personal protective equipment should be used when handling the compound.
Specific safety guidelines and recommendations can be found in the safety data sheet (SDS) provided by the manufacturer.
N,N-Dimethylbenzylamine is often employed as a catalyst in various chemical reactions.
N,N-Dimethylbenzylamine is catalytic properties make it valuable in promoting specific chemical transformations.
One significant application involves the quaternization reaction, where N,N-Dimethylbenzylamine is reacted with an alkyl halide to produce a quaternary ammonium salt.
These salts have applications in various chemical processes, including as surfactants and phase transfer catalysts.
Quaternary ammonium compounds derived from N,N-Dimethylbenzylamine may exhibit surfactant properties, making them useful in formulations such as detergents, fabric softeners, and other cleaning products.
Uses Of N,N-Dimethylbenzylamine:
N,N-Dimethylbenzylamine is used as a chemical reagent in various laboratory procedures, including organic synthesis and analytical chemistry.
N,N-Dimethylbenzylamine may be incorporated into resin formulations, contributing to the curing process and modifying the properties of the final cured resin.
Some derivatives of N,N-Dimethylbenzylamine find applications in pharmaceuticals, either as intermediates or as components in drug formulations.
N,N-Dimethylbenzylamine may serve as a complexing agent in certain chemical processes, forming stable complexes with metal ions.
N,N-Dimethylbenzylamine is utilized in research and development for the synthesis of novel materials, compounds, and chemical processes.
N,N-Dimethylbenzylamine plays a role in the formulation of adhesives, influencing the curing and adhesive properties of the final product.
N,N-Dimethylbenzylamine was used in the synthesis of bis[(N,N-dimethylamino)benzyl] selenide.
N,N-Dimethylbenzylamine has been used as catalyst during curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.
N,N-Dimethylbenzylamine undergoes directed ortho metalation with butyl lithium.
N,N-Dimethylbenzylamine reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts.
Further, N,N-Dimethylbenzylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.
N,N-Dimethylbenzylamine is used in the production of polyurethane paints , coatings, foams and potting compounds and as an intermediate in organic syntheses.
N,N-Dimethylbenzylamine is also used in electron microscopy as a so-called Maraglas catalyst.
As the molecule has tertiary amine functionality, two of the key uses are as an epoxy-amine cure enhancement catalyst and also as a polyurethane catalyst.
N,N-Dimethylbenzylamine , can be ligated with a N-heterocyclic carbene, to produce a highly active, practical and versatile catalyst for the Heck-Mizoroki reaction.
N,N-Dimethylbenzylamine can also be used for the perpetration of novel electrolyte, dibenzyldimethylammonium fluoride for acylation of cellulose.
N,N-Dimethylbenzylamine is employed as a curing agent in the formulation of resins, contributing to the polymerization process and modifying the properties of the cured resin.
N,N-Dimethylbenzylamine may be involved in polymerization reactions, contributing to the synthesis of polymers with specific characteristics.
N,N-Dimethylbenzylamine can act as a solvent in certain chemical reactions, aiding in the dissolution and mixing of reactants.
Some quaternary ammonium compounds derived from N,N-Dimethylbenzylamine possess antimicrobial properties, making them suitable for use in disinfectants and sanitizers.
Quaternary ammonium salts obtained from N,N-Dimethylbenzylamine may be used for pH regulation in various formulations.
Quaternary ammonium compounds derived from N,N-Dimethylbenzylamine are employed in fabric softeners, enhancing the softness of fabrics and reducing static cling.
N,N-Dimethylbenzylamine may find applications in the oil and gas industry, particularly in certain chemical processes and formulations.
N,N-Dimethylbenzylamine can be used in metalworking processes to provide corrosion protection for metal surfaces.
N,N-Dimethylbenzylamine is utilized as an additive in certain industrial fluids to modify their properties.
In the oil and gas sector, N,N-Dimethylbenzylamine is sometimes used as a hydrogen sulfide scavenger to mitigate the corrosive effects of hydrogen sulfide.
N,N-Dimethylbenzylamine may serve as an additive in certain fuels to improve combustion properties.
N,N-Dimethylbenzylamine may be used in the synthesis of certain photographic chemicals.
N,N-Dimethylbenzylamine can be involved in the manufacturing of dyes and related compounds.
N,N-Dimethylbenzylamine can be used as a chemical intermediate in the synthesis of various compounds.
N,N-Dimethylbenzylamine may serve as a catalyst or a reactant in certain chemical reactions.
N,N-Dimethylbenzylamine can be further reacted to form quaternary ammonium salts, which have applications in various chemical processes.
N,N-Dimethylbenzylamine is used as a catalyst in various chemical reactions, particularly in organic synthesis.
N,N-Dimethylbenzylamine serves as an intermediate in the production of quaternary ammonium compounds, which find applications in the synthesis of surfactants and other specialty chemicals.
In some cases, N,N-Dimethylbenzylamine may be used as a corrosion inhibitor.
N,N-Dimethylbenzylamine is often employed as a catalyst in various chemical reactions, facilitating the transformation of reactants into products.
N,N-Dimethylbenzylamine is a key intermediate in the synthesis of quaternary ammonium salts.
These salts have applications as surfactants, phase transfer catalysts, and antimicrobial agents.
Some quaternary ammonium compounds derived from N,N-Dimethylbenzylamine exhibit surfactant properties.
These compounds are used in formulations such as detergents, fabric softeners, and cleaning products.
In polymer chemistry, N,N-Dimethylbenzylamine can be used as an additive to modify the properties of certain polymers.
N,N-Dimethylbenzylamine finds applications in adhesive formulations, influencing the curing process and adhesive properties of the final product.
N,N-Dimethylbenzylamine can act as a corrosion inhibitor in certain industrial applications, helping to protect metal surfaces from corrosion.
Safety Profile Of N,N-Dimethylbenzylamine:
N,N-Dimethylbenzylamine should be handled with care as it is a chemical substance, and exposure to skin, eyes, or inhalation should be avoided.
Poison by ingestion.
Moderately toxic by inhalation and skin contact.
A severe eye and skin irritant.
Flammable when exposed to heat or flame.
When heated to decomposition it emits toxic fumes of NOx.
The vapors of N,N-Dimethylbenzylamine can form an explosive mixture with air ( flash point 55 °C, ignition temperature 410 °C).
Proper safety precautions, including the use of personal protective equipment, should be followed when working with this compound.
The specific hazards and safety guidelines may vary, and it's crucial to refer to the safety data sheet (SDS) provided by the manufacturer or supplier.
