What color is 2 6 dimethylaniline?
colorless
2,6-Xylidine is an organic compound with the formula C6H3(CH3)2NH2. It is one of several isomeric xylidines. It is a colorless viscous liquid.
What are hazards with 2 6 dimethylaniline?
It has a role as a carcinogenic agent and a drug metabolite. It is a primary arylamine and a dimethylaniline. 2,6-xylidine appears as a liquid. Toxic by ingestion, inhalation and skin absorption.
What is the density of 2 6 dimethylaniline?
984 kg/m³
2,6-Xylidine/Density
What is xylidine used for?
Xylidines are used in production of pigments and dyestuffs, and various antioxidants, agrochemicals, pharmaceuticals, hypergolic propellants, and many other organic chemicals.
Is N N dimethylaniline soluble in water?
N,n-dimethylaniline appears as a yellow to brown colored oily liquid with a fishlike odor. Less dense than water and insoluble in water.
What is the density of N N dimethylaniline?
956 kg/m³
Dimethylaniline/Density
What is the formula of dimethylaniline?
C₈H₁₁N
Dimethylaniline/Formula
Is nn dimethylaniline acidic or basic?
Dimethylaniline undergoes many of the reactions expected for an aniline, being weakly basic and reactive toward electrophiles.
Why aniline is a weaker base?
Basically, aniline is considered as the simplest aromatic amine. Now, aniline is considered as a weaker base than ammonia. This is due to the fact that the lone pair in aniline are involved in resonance with the benzene ring and hence are not available for donation to that extent as in NH3.
Which compound does not show diazo?
Benzylamine is a 1∘ aliphatic amiine and hence does not undergo diazotisation.
What is the purpose of 2, 6-dimethylaniline?
2,6-dimethylaniline is a primary arylamine that is aniline in which the hydrogens at the 2- and 6-positions are replaced by methyl groups. It is used in the production of some anasthetics and other chemicals.
Where is 2, 6-dimethylaniline found in cigarette smoke?
2,6-Dimethylaniline is found in cigarette smoke; it is a pharmacologically inactive metabolite of some drugs (e.g., the local anesthetic lidocaine) and pesticides (e.g., metalaxyl); and it is an impurity in technical grade metalaxyl. (1)
How is 2, 6-dimethylaniline methylated to mepivacaine?
The resulting 2,6-xylidide α -pipecolinic acid (2.2.5) is methylated to mepivacaine using formaldehyde with simultaneous reduction by hydrogen in the presence of platinum on carbon catalyst [ 15 ]. Mepivacaine is similar to lidocaine in terms of properties; however, it has longer lasting effects.
What is the synthesis of 2, 6-dimethylaniline bromide?
According to the first, mepivacaine is synthesized by reacting the ethyl ester of 1-methylpiperindine-2-carboxylic acid with 2,6-dimethylanilinomagnesium bromide, which is synthesized from 2,6-dimethylaniline and ethylmagnesium bromide [12–14 ].