N,N-DIMETHYLANILINE
N,N-DIMETHYLANILINE
N,N-Dimethylaniline = DMA = Dimethylaniline
CAS Number: 121-69-7
EC Number: 204-493-5
Molecular Weight: 121.18
Linear Formula: C6H5N(CH3)2
N,N-Dimethylaniline (DMA) is an organic chemical compound, a substituted derivative of aniline.
N,N-Dimethylaniline consists of a tertiary amine, featuring dimethylamino group attached to a phenyl group.
This oily liquid ,N,N-Dimethylaniline, is colourless when pure, but commercial samples are often yellow.
N,N-Dimethylaniline is an important precursor to dyes such as crystal violet.
N,N-Dimethylaniline, also known as dimethylaminobenzene or dimethylphenylamine, belongs to the class of organic compounds known as dialkylarylamines.
These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
N,N-dimethylaniline is a tertiary amine that is aniline in which the amino hydrogens are replaced by two methyl groups.
N,N-Dimethylaniline is a tertiary amine and a dimethylaniline.
N,N-dimethylaniline appears as a yellow to brown colored oily liquid with a fishlike odor.
N,N-Dimethylaniline is less dense than water and insoluble in water.
N,N-Dimethylanilines flash point is 150 °F, and is toxic by ingestion, inhalation, and skin absorption.
N,N-Dimethylaniline was used to make dyes and as a solvent.
Outside of the human body, N,N-Dimethylaniline has been detected, but not quantified in several different foods, such as common mushrooms, strawberries, feijoa, limes, and black-eyed pea.
Applications of N,N-Dimethylaniline:
DMA is a key precursor to commercially important triarylmethane dyes such as malachite green and crystal violet.
DMA serves as a promoter in the curing of polyester and vinyl ester resins.
DMA is also used as a precursor to other organic compounds.
A study of the in vitro metabolism of N,N-dimethylaniline using guinea pig and rabbit preparations and GLC techniques has confirmed N-demethylation and N-oxidation as metabolic pathways, and has also established ring hydroxylation as a metabolic route.
N,N-Dimethylanilines derivative 2,4-dimethylaniline is a recalcitrant degradant of the pesticide amitraz and is also an industrial pollutant which is genotoxic, teratogenic and carcinogenic.
N,N-Dimethylaniline is a tertiary amine used in the synthesis of several triarylmethane dyes like malachite green.
N,N-Dimethylaniline is also used in the synthesis of a magnetic gram stain for the detection of bacteria.
Preparation and reactions of N,N-Dimethylaniline:
DMA was first reported in 1850 by the German chemist A. W. Hofmann, who prepared it by heating aniline and iodomethane:
C6H5NH2 + 2 CH3I → C6H5N(CH3)2 + 2 HI
DMA is produced industrially by alkylation of aniline with methanol in the presence of an acid catalyst:
C6H5NH2 + 2 CH3OH → C6H5N(CH3)2 + 2 H2O
Similarly, N,N-Dimethylaniline is also prepared using dimethyl ether as the methylating agent.
Dimethylaniline undergoes many of the reactions expected for an aniline, being weakly basic and reactive toward electrophiles.
For example, N,N-Dimethylaniline is nitrated to produce tetryl, a derivative with four nitro groups which was once used as explosive.
N,N-Dimethylaniline is lithiated with butyllithium.
Methylating agents attack the amine to give the quaternary ammonium salt:
C6H5N(CH3)2 + (CH3O)2SO2 → C6H5N(CH3)3CH3OSO3
Applications of N,N-Dimethylaniline:
N,N-Dimethylaniline is a tertiary amine used in the synthesis of several triarylmethane dyes like malachite green.
N,N-Dimethylaniline is also used in the synthesis of a magnetic gram stain for the detection of bacteria.
CAS Number: 121-69-7
CHEBI: 16269
ChEMBL: ChEMBL371654
ChemSpider: 924
ECHA InfoCard: 100.004.085
KEGG: C02846
PubChem CID: 949
UNII: 7426719369
CompTox Dashboard (EPA): DTXSID2020507
N, N-Dimethylaniline is an organic chemical compound, a substituted derivative of aniline.
N,N-Dimethylaniline consists of a tertiary amine, featuring dimethylamino group attached to a phenyl group.
N,N-Dimethylaniline is colourless when pure, but commercial samples are often yellow.
What is N in NN dimethylaniline?
Definition: A tertiary amine that is aniline in which the amino hydrogens are replaced by two methyl groups.
Chemical Properties of N,N-Dimethylaniline:
Straw to brown-colored oily liquid with a characteristic amine-like odor.
Odor threshold concentration is 13 ppb (quoted, Amoore and Hautala, 1983).
Uses of N,N-Dimethylaniline:
N,N-Dimethylaniline is used in production of dyestuffs, as a solvent, a reagent in methylation reactions, and a hardener in fiberglass reinforced resins.
Intermediate in the manufacture of dyes; solvent; rubber vulcanizing agent and stabilizer
Solvent; manufacture of vanillin, Michler’s ketone, methyl violet and other dyes. As reagent for methanol, methyl furfural, H2O2, nitrate, alcohol, formaldehyde.
Industrial uses of N,N-Dimethylaniline:
N,N-Dimethylaniline is used as chemical intermediate in the manufacturing of vanillin, Michler’s ketone, and dyes such as Acid Red 2, Basic Green 4 and Basic Violet 1.
N,N-Dimethylaniline is also used as a solvent and an activator for polyesters and as an alkylating agent.
N,N-Dimethylaniline is used as an acid scavenger or accepter in the manufacture of beta-lactam antibiotics such as penicillin and cephalosporin.
Definition of N,N-Dimethylaniline:
ChEBI: A tertiary amine that is aniline in which the amino hydrogens are replaced by two methyl groups.
Appearance of N,N-Dimethylaniline：
N,n-dimethylaniline appears as a yellow to brown colored oily liquid with a fishlike odor.
Production Methods of N,N-Dimethylaniline:
N,N-Dimethylaniline is made by heating aniline, methyl alcohol and sulfuric acid under pressure, followed by hydrolysis of the sulfate formed with sodium hydroxide to the free base (Windholz et al 1983).
United States production in 1975 was estimated at 4,600 metric tons.
General Description of N,N-Dimethylaniline:
A yellow to brown colored oily liquid with a fishlike odor.
Less dense than water and insoluble in water.
Flash point 150°F.
Toxic by ingestion, inhalation, and skin absorption.
N,N-Dimethylaniline is used to make dyes and as a solvent.
Air & Water Reactions of N,N-Dimethylaniline:
Insoluble in water.
Reactivity Profile of N,N-Dimethylaniline:
Explosive decomposition occurred when finely divided benzoyl peroxide was allowed to react with N,N-Dimethylaniline by breaking an ampoule containing 0.5 grams of dimethylaniline in an autoclave, NFPA 491M, 1991.
This result may be expected with other peroxides and various oxidants.
Uses of N,N-Dimethylaniline:
N,N-Dimethylaniline is used as an intermediate in the manufacture of vanillin, Michler’s ketone, methyl violet and other dyes and also as a solvent, an alkylating agent, and a stabilizer.
N,N-Dimethylaniline was one of the earliest substrates for reduction examined by Birch.
This and subsequent studies have shown that a variety of aniline derivatives are reduced initially to the 2,5-dihydro derivatives, but also that these are easily isomerized to the 2,3-dihydro isomers either in situ (leading to tetrahydro derivatives) or during work-up procedures.
The dienamines formed in this way may be hydrolyzed to cyclohexenones, treated with electrophiles, or utilized in [4 + 2] cycloadditions.
The less basic morpholino dienamines are more stable and afford the most reliable outcomes.
Which of the following is N N-dimethylaniline?
N,N-dimethylaniline is a tertiary amine that is aniline in which the amino hydrogens are replaced by two methyl groups.
N,N-Dimethylaniline is a tertiary amine and a dimethylaniline. N,N-Dimethylaniline is used as an intermediate in the manufacture of dyes and other substances.
What is dimethylaniline used for?
Dimethylaniline is a yellow to brownish, oily liquid with a fish- like odor.
N,N-Dimethylaniline is used as a solvent and in making other chemicals and dyes.
Is N N-dimethylaniline aromatic?
N,N-Dimethylaniline, also known as dimethylaminobenzene or dimethylphenylamine, belongs to the class of organic compounds known as dialkylarylamines.
These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
Chemical formula: C8H11N
Molar mass: 121.183 g·mol−1
Appearance: Colorless liquid
Odor: amine-like
Density: 0.956 g/mL
Melting point: 2 °C (36 °F; 275 K)
Boiling point: 194 °C (381 °F; 467 K)
Solubility in water: 2% (20°C)
Vapor pressure: 1 mmHg (20°C)
Magnetic susceptibility (χ): -89.66·10−6 cm3/mol
Physical Properties of N,N-Dimethylaniline:
-The chemical formula for N,N-dimethylaniline is C8H11N, and its molecular weight is 121.18 g/mol.
-N,N-Dimethylaniline occurs as a yellow oily liquid that is insoluble in water.
-The odor threshold for N,N-dimethylaniline is 0.013 parts per million (ppm).
-The vapor pressure for N,N-dimethylaniline is 0.52 mm Hg at 25 °C, and its log octanol/water partitioncoefficient (log Kow) is 2.31.
Usage of N,N-Dimethylaniline:
N,N-Dimethylaniline is used in production of dyestuffs, as a solvent, a reagent in methylation reactions, and a hardener in fiberglass reinforced resins.
Solvent; manufacture of vanillin, Michler’s ketone, methyl violet and other dyes.
As reagent for methanol, methyl furfural, H2O2, nitrate, alcohol, formaldehyde.
Boiling point: 192 – 195 °C (1013 hPa)
Density: 0.956 g/cm3
Explosion limit: 1.2 – 7 %(V)
Flash point: 75 °C
Ignition temperature: 370 °C DIN 51794
Melting Point: 1.5 – 2.5 °C
pH value: 7.4 (1.2 g/l, H₂O, 20 °C)
Vapor pressure: 13 hPa (70 °C)
Solubility: 1.2 g/l
Why does the dimethylaniline couple with the diazonium salt at the para position of the ring?
The somewhat bulky dimethylamino group does make it more difficult for an electrophile to approach the ortho position and the diazonium ion is relatively large.
These two steric factors combine to reduce the amount of the ortho isomer and the para isomer predominates.
What is the structure of 5 chloro 4 methoxy 2 nitrophenol?
N-(5-Chloro-4-methoxy-2-nitrophenyl)acetamide | C9H9ClN2O4.
Why is n n 2 6 Tetramethylaniline a stronger base than N N dimethylaniline?
The stronger base is the one that has greater tendency to donate lone pair of electrons.
N,N,2,6-tetramethyl aniline is a stronger base than N,N-dimethyl aniline because of +I effect of all attached CH.
CH3 shows +I effect as well as hyperconjugation due to which it increases electron density of the benzene ring.
What is the pKb value of aniline?
The pKb values of ammonia, methenamine and benzenamine (aniline) are 4.75, 3.38 & 9.38 respectively.
Electrochemical oxidation and polymerization of N,N-dimethylaniline at a gold electrode have been studied in an acidic solution.
Both potential cycling and electrolysis at a controlled potential yield a thin film of a polymer that shows electrochemical activity in acidic and pH-neutral solutions.
Raman spectra of sulfate- and polystyrenesulfonate-doped polymer have been obtained and analyzed.
Two possibilities for electropolymerization have been considered – a simple polymerization yielding a “true” poly(N,N-dimethylaniline), and polymerization accompanied by a partial demethylation yielding poly(N-methylaniline).
Based on the results obtained, the first one has been considered as most likely.
Purification Methods of N,N-Dimethylaniline:
Primary and secondary amines (including aniline and monomethylaniline) can be removed by refluxing for 4-5hours with excess acetic anhydride, and then fractionally distilling.
Crocker and Jones used four volumes of acetic anhydride, then distilled off the greater part of it, and dissolved the residue in ice-cold dilute HCl.
Non-basic materials were removed by ether extraction, then the dimethylaniline was liberated with ammonia, extracted with ether, dried, and distilled under reduced pressure.
Metzler and Tobolsky refluxed with only 10% (w/w) of acetic anhydride, then cooled and poured it into excess 20% HCl, which, after cooling, was extracted with diethyl ether.
The HCl solution was cautiously made alkaline to phenolphthalein, and the amine layer was drawn off, dried over KOH and fractionally distilled under reduced pressure, under nitrogen.
Suitable drying agents for dimethylaniline include NaOH, BaO, CaSO4, and CaH2.
Other purification procedures include the formation of the picrate (m 163o from Me2CO or EtOH/H2O), prepared in *benzene solution and crystallised to constant melting point, then decomposed with warm 10% NaOH and extracted into ether: the extract was washed with water and distilled under reduced pressure.
The oxalate salt has also been used for purification.
The base has been fractionally crystallised by partial freezing and also from aqueous 80% EtOH then from absolute EtOH.
It has been distilled from zinc dust, under nitrogen.
CAS: 121-69-7
EINECS: 204-493-5
Molecular Formula: C8H11N
Molecular Weight: 121.18
Appearance: liquid
density: 0.956 g/mL at 20 °C
mp: 1.5-2.5 °C(lit.)
bp: 193-194 °C(lit.)
vapor density: 3 (vs air)
vapor pressure: 2 mm Hg ( 25 °C)
Fp: 158 °F
Stability: Stable.
Water Solubility: 1 g/L (20 ºC)
Is N,N-Dimethylaniline acidic or basic?
Dimethylaniline undergoes many of the reactions expected for an aniline, being weakly basic and reactive toward electrophiles.
Is dimethylaniline soluble in water?
Solubility : Soluble in water (1.2 g/l) at 20° C, ethanol, ether, acetone, chloroform, benzene, and Alkaline.
How do you convert benzene to nn dimethylaniline?
Hint: the benzene is nitrated followed by the reduction in presence of H2/Pd. the aniline formed further reacted in presence of chloroform CH3I such that each hydrogen of the aniline is replaced by methyl −CH3to produce the N, N – dimethylaniline.
Which is more basic N methylaniline or NN dimethylaniline?
N,N-Dimethylaniline is more basic than aniline as lone pair will increase the basicity and again the methyl griup over aniline will increase the electron cloud .
What hazard does N N-dimethylaniline present?
Acute (short-term) inhalation exposure to N,N-dimethylaniline has resulted in effects on the central nervous system (CNS) and circulatory system, with headache, cyanosis, and dizziness in humans.
Effects on the blood have been reported in exposed workers.
A route for the direct synthesis of N,N-dimethylaniline from nitrobenzene and methanol was developed through the sequential coupling of the hydrogen production from methanol, hydrogenation of nitrobenzene to produce aniline, and N-methylation of aniline over a pretreated Raney-Ni catalyst (at 443 K in methanol).
A high yield of N,N-dimethylaniline up to 98% was obtained by the proposed methodology.
In this process, aniline was produced from in-situhydrogenation of nitrobenzene with hydrogen generated from methanol, or transfer hydrogenation of nitrobenzene with methanol as donor, while methanol acted as a hydrogen source, alkylating reagent and solvent, simultaneously.
Additionally, a plausible mechanism of this one-pot reaction process has been described.
Storage of N,N-Dimethylaniline:
Store in a cool, dry place.
Store in a tightly closed container.
Flammables-area. Do not store in metal containers.
Handling of N,N-Dimethylaniline:
Wash thoroughly after handling. Wash hands before eating.
Remove contaminated clothing and wash before reuse.
Use with adequate ventilation. Ground and bond containers when transferring material.
Empty containers retain product residue, (liquid and/or vapor), and can be dangerous.
Do not get on skin or in eyes.
Avoid ingestion and inhalation.
Do not pressurize, cut, weld, braze, solder, drill, grind, or expose empty containers to heat, sparks or open flames.
Protection of N,N-Dimethylaniline:
Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA’s eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin: Wear appropriate protective gloves to prevent skin exposure.
Clothing: Wear appropriate protective clothing to prevent skin exposure.
How many constitutional isomers of dimethylaniline where the methyl groups are on the aromatic ring are possible?
There are six structural isomers.
The names of six compounds indicate methyl group positions relative to the amino on the benzene ring.
What is nn chemistry?
N,N-Diisopropylethylamine, or Hünig’s base, is an organic compound and an amine.
N,N-Dimethylaniline is used in organic chemistry as a base.
Why aniline is insoluble in water?
Aniline is insoluble in water because of the large hydrocarbon part that retards the formation of an H-bond.
So N,N-Dimethylaniline is insoluble in water.
Anilines are the organic compounds in the class of group coming in organic chemistry which are also called aminobenzene or phenylamine.
What color is 2 6 dimethylaniline?
YELLOW LIQUID WITH CHARACTERISTIC ODOUR.
What are hazards with 2 6 dimethylaniline?
Harmful by inhalation, in contact with skin and if swallowed.
Irritating to respiratory system and skin.
Vapors may cause dizziness or suffocation.
Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Respirators:
Follow the OSHA respirator regulations found in 29CFR 1910.134 or European Standard EN 149.
Always use a NIOSH or European Standard EN 149 approved respirator when necessary.
Small spills/leaks: Absorb spill with inert material, (e.g., dry sand or earth), then place into a chemical waste container.
Avoid runoff into storm sewers and ditches which lead to waterways.
Clean up spills immediately, using the appropriate protective equipment.
Scoop up with a nonsparking tool, then place into a suitable container for disposal.
Remove all sources of ignition. Do not get water inside containers.
Disposal code:9
Stability:
Stable under normal temperatures and pressures.
Incompatibilities:
Metals, water, strong oxidizing agents.
Decomposition:
Carbon monoxide, oxides of nitrogen, irritating and toxic fumes and gases, carbon dioxide, hydrogen gas.
Quality Level: 200
product line: ReagentPlus®
assay: 99%
form: liquid
refractive index: n20/D 1.557 (lit.)
pH: 7.4 (20 °C, 1.2 g/L)
bp: 193-194 °C (lit.)
mp: 1.5-2.5 °C (lit.)
density: 0.956 g/mL at 25 °C (lit.)
application(s): microbiology
SMILES string: CN(C)c1ccccc1
InChI: 1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3
InChI key: JLTDJTHDQAWBAV-UHFFFAOYSA-N
Preferred IUPAC name:
N,N-Dimethylaniline
Other names:
DMA
Dimethylaminobenzene
N,N-Dimethylbenzeneamine
N,N-Dimethylphenylamine
N, N-Dimethylaniline (DMA) CAS NO. 121-69-7 N,N-dimethylaniline, also known as N,N-dimethylaniline, dimethylaminobenzene and dimethylaniline.
N,N-Dimethylaniline is a yellow oily liquid, insoluble in water, soluble in ethanol, ether.
N,N-Dimethylaniline is mainly used as dye intermediates, solvents, stabilizers, analytical reagents.
N,N-Dimethylaniline application as curing agent for epoxy resin, as intermediate for organic synthesis, used in the preparation of quatemary amine, dehydrogenation catalyst, preservative and neutralizing agent.
MDL number: MFCD00008304
PubChem Substance ID: 57651326
NACRES: NA.22
Beilstein: 507140
Formula: C8H11N / C6H5N(CH3)2
Molecular mass: 121.2
Boiling point: 192-194°C
Melting point: 2.5°C
Relative density (water = 1): 0.96
Solubility in water: none
Vapour pressure, Pa at 20°C: 67
Relative vapour density (air = 1): 4.2
Relative density of the vapour/air-mixture at 20°C (air = 1): 1.002
Flash point: 62°C
Auto-ignition temperature: 371°C
Explosive limits, vol% in air: 1-7
Octanol/water partition coefficient as log Pow: 2.3
N,N-dimethylaniline
121-69-7
Dimethylphenylamine
Benzenamine, N,N-dimethyl-
N,N-Dimethylbenzenamine
(Dimethylamino)benzene
N,N-Dimethylphenylamine
N,N-Dimethylbenzeneamine
Dimethylaminobenzene
Dwumetyloanilina
N,N-(Dimethylamino)benzene
N,N-dimethylanilin
Aniline, N,N-dimethyl
Versneller NL 63/10
Dimethyl-phenyl-amine
NCI-C56428
NSC 7195
NL 63-10P
N,N-Dimethyl-N-phenylamine
N,N-DIMETHYL-ANILINE
UNII-7426719369
CHEBI:16269
DSSTox_CID_507
DSSTox_RID_75629
DSSTox_GSID_20507
Dimethylaniline, N,N-
dimethyl aniline
Dwumetyloanilina [Polish]
CAS-121-69-7
N-N-Dimethylaniline
CCRIS 2381
N, N-Dimethylaniline
HSDB 1179
N,N-dimethylaminobenzene
EINECS 204-493-
UN2253
dimethyl-aniline
AI3-17284
n-dimethylaniline
N,N-Dmethylanlne
N,N-dimethyaniline
N,N-dimethylamline
N,N dimethylaniline
N,N-dimethylaniiine
PhNMe2
n,n,-dimethylaniline
N,N-dirnethylaniline
N,N-dimethyl aniline
N,N-dimethyl-Benzenamine
ACMC-1AU9Z
EC 204-493-5
N,N-Dimethylaniline sulfate
PhN(CH3)2
SCHEMBL8277
N,N-Dimethylaniline, 99%
MLS002222341
BIDD:ER0332
N,N-Dimethyl-N-phenylamine #
CHEMBL371654
DTXSID2020507
N,N-Dimethylaniline [UN2253]
N,N-dimethylaniline,sulfuric acid
NSC7195
WLN: 1N1 & R
NSC-7195
N,N-Dimethylaniline, LR, >=99%
Tox21_201813
Tox21_300036
MFCD00008304
STL268843
ZINC12358697
AKOS000119088
MCULE-7231102072
UN 2253
NCGC00090724-01
NCGC00090724-02
NCGC00090724-03
NCGC00254056-01
NCGC00259362-01
LS-13434
SMR001252235
N,N-Dimethylaniline [UN2253] [Poison]
N,N-Dimethylaniline, ReagentPlus(R), 99%
D0665
D3866
N,N-Dimethylaniline, for synthesis, 99.5%
6124-EP0930075A1
6124-EP2269977A2
6124-EP2269989A1
6124-EP2275411A2
6124-EP2281563A1
6124-EP2281815A1
6124-EP2281817A1
6124-EP2284174A1
6124-EP2287160A1
6124-EP2287165A2
6124-EP2287166A2
6124-EP2289868A1
6124-EP2292620A2
6124-EP2295415A1
6124-EP2295430A2
6124-EP2295431A2
6124-EP2298731A1
6124-EP2298750A1
6124-EP2298763A1
6124-EP2298772A1
6124-EP2298774A1
6124-EP2301926A1
6124-EP2301933A1
6124-EP2305633A1
6124-EP2305647A1
6124-EP2308562A2
6124-EP2308839A1
6124-EP2308857A1
6124-EP2308867A2
6124-EP2308870A2
6124-EP2308926A1
6124-EP2311827A1
6124-EP2314586A1
6124-EP2374783A1
6124-EP2377813A1
6124-EP2377841A1
6124-EP2380869A1
6124-EP2380870A1
C02846
D95371
23555-EP2280000A1
23555-EP2281818A1
23555-EP2284169A
23555-EP2284174A1
23555-EP2287161A1
23555-EP2287162A1
23555-EP2287165A2
23555-EP2287166A2
23555-EP2292597A1
23555-EP2292606A1
23555-EP2292620A2
23555-EP2298768A1
23555-EP2314582A1
23555-EP2371811A2
135609-EP2277868A1
135609-EP2277869A1
135609-EP2277870A1
135609-EP2292608A1
162125-EP2281821A1
N,N-Dimethylaniline, SAJ first grade, >=99.0%
Q310473
J-004597
J-523266
F0001-0348
N,N-Dimethylaniline [ACD/IUPAC Name]
121-69-7 [RN]
204-493-5 [EINECS]
86362-18-7 [RN]
aniline, N,N-dimethyl-
Benzenamine, N,N-dimethyl- [ACD/Index Name]
Benzenamine, N,N-dimethyl-, radical ion(1-)
dimethylaniline [Wiki]
Dimethylaniline, N,N-
Dimethylaniline, N-N-
MFCD00008304 [MDL number]
N,N-Dimethylanilin [German] [ACD/IUPAC Name]
N,N-DIMETHYL-ANILINE
N,N-Diméthylaniline [French] [ACD/IUPAC Name]
N,N-dimethyl-Benzenamine
(dimethylamino)benzene
210-769-6 [EINECS]
25052-92-0 [RN]
4019-61-8 [RN]
85785-00-8 [RN]
87385-38-4 [RN]
dimethyl aniline
Dimethylaminobenzene
dimethylphenylamine
dimethyl-phenyl-amine
DMA
Dwumetyloanilina
N, N, DIMETHYLANILINE
N,N-(Dimethylamino)benzene
N,N-DIMETHYLAMINOBENZENE
N,N-Dimethylaniline-d11
N,N-Dimethylbenzenamine
N,N-Dimethylbenzeneamine
N,N-Dimethyl-N-phenylamine
N,N-Dimethylphenylamine
N,N-二甲基苯胺 [Chinese]
NL 63-10P
N-Phenyldimethylamine
N,N-Dimethylaniline, purified by redistillation, >=99.5%