3,4-Dimethylaniline

HCID 7248CAS 95-64-7

Basic information

Standard SMILES
Cc1ccc(N)cc1C
InChIKey
DOLQYFPDPKPQSS-UHFFFAOYSA-N
Molecular formula
C8H11N
Average molar mass
121.18 g/mol
Monoisotopic mass
121.08914935

Overview

3,4-xylidine appears as pale brown crystals or off-white solid. (NTP, 1992)

Names & identifiers

Preferred name
3,4-Dimethylaniline
IUPAC
3,4-dimethylaniline
English name
3,4-Dimethylaniline
Molecular formula
C8H11N
Molecular weight
121.18

Names & synonyms

3,4-Dimethylaniline95-64-73,4-XYLIDINE4-Amino-o-xylene3,4-Dimethylbenzenamine3,4-XylylamineBenzenamine, 3,4-dimethyl-1-Amino-3,4-dimethylbenzene3,4-Dimethylphenylamine3,4-Dimethylaminobenzene4-Amino-1,2-dimethylbenzene3,4-Dimethylbenzeneamine
Show more names
AKOS 91143ASYM-O-XYLIDINEAKOS BBS-000036733,4-DitolueneAmine
DTXSID30263083,4-dimethylbenzene-1-amineBenzene, 4-amino-1,2-dimethyl-R27I33AIDTAI3-22779NSC-41800DTXCID406308CHEBI:39901

Database identifiers

CAS
95-64-7
PubChem CID
7248
DTXSID
DTXSID3026308
ChEMBL
CHEMBL1230039
ChEBI
CHEBI:39901
UNII
R27I33AIDT
EC Number
202-437-4
Nikkaji
J357C

Properties

Computed structural properties

XLogP
2.5
Topological polar surface area
26 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
9

Experimental & physicochemical properties

DrugsPharmaceuticals -> Listed in ZINC15
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP · 3 items

log Kow= 1.84

1.84

1.86

Density · 3 items

1.076 at 64 °F (NTP, 1992) - Denser than water; will sink

1.076 @ 18 °C

Relative density (water = 1): 1.07

Color/Form · 2 items

Plates of prisms from petroleum ether

Crystalline solid

Solubility · 5 items

less than 1 mg/mL at 66 °F (NTP, 1992)

Sol in ether, petroleum

Very soluble in ligroin; soluble in ether; slightly soluble in chloroform and water.

Soluble in aromatic solvents.

Solubility in water, g/100ml at 22 °C: 0.38

Physicochemical properties

Melting point
49 · 49-51 °C(lit.)
Boiling point
226 °C · 226 °C(lit.)
Density
1.076 · 1.076
vapor pressure
3.72 Pa · 3.72Pa at 25℃
refractive index
1.5135 · 1.5135 (estimate)
Flash point
209 °F · 209 °F

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H301 (96.3%): Toxic if swallowed [Danger Acute toxicity, oral]

P260, P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P319, P321, P330, P361+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 54 reports by companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

Hazard information

Regulatory Information · 3 items

Chemical: Benzenamine, 3,4-dimethyl-

Status: Cease Manufacture Update: 11-05-2012 https://echa.europa.eu/registration-dossier/-/registered-dossier/10998

3,4-Dimethylaniline: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Xylidines: Human health tier II assessment
DOT LabelPoison
Fire Hazards · 2 items

This chemical is combustible. (NTP, 1992)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Above 98 °C explosive vapour/air mixtures may be formed.

Health Hazards · 1 item

SYMPTOMS: Symptoms of exposure to this compound may include headaches, drowsiness, cyanosis, mental confusion, convulsions, anorexia, nervous system and blood effects, fatigue, loss of appetite, dizziness, and damage to the lungs, liver and kidneys.

Hazards Summary · 1 item

The major hazards encountered in the use and handling of 3,4-xylidine stem from its toxicologic properties. Toxic by all routes (ie, inhalation, ingestion, and dermal absorption), exposure to this crystalline material may occur from its use as a chemical intermediate for the synthesis of riboflavin (vitamin B2). Contact with 3,4-xylidine may cause burns to the skin and eyes. Death is also a possible outcome from exposure. While the OSHA PEL is set at a TWA of 5 ppm, the ACGIH lists xylidine (mixed isomers) on its 1988-1989 Notice of Intended Changes with a proposed TLV of 0.5 ppm, and a designation of "suspected human carcinogen". In activities or situations where over-exposure may occur, wear a self-contained breathing apparatus, and full chemical protective clothing which is specifically recommended by the shipper or manufacturer to prevent skin contact with xylidine. If contact should occur, immediately flush the affected skin or eyes with running water for at least 15 minutes. Remove contaminated clothing and shoes at the site. Do not eat or smoke in xylidine work areas. While xylidine does not ignite easily, it can burn with the production of irritating or poisonous gases. Also, containers may explode violently in the heat of a fire. Fires involving xylidine may be extinguished with dry chemical, CO2, Halon, or standard foam. Water spray if used, should be applied with caution because it may cause frothing. Fight the fire from a maximum distance and dike runoff from fire control water. Xylidine should be stored away from heat, strong oxidizers, and hypochlorite bleaches. Shipping regulations and other DOT regulatory requirements should be consulted before transport. If 3,4-xylidine should spill, carefully shovel the material into clean covered containers (solutions are first diked far ahead, then taken up with sand or other noncombustible absorbent) for later disposal. Incineration is a possible form of disposal for xylidine. Before implementing land disposal of waste 3,4-xylidine, consult with environmental regulatory agencies for guidance.

Safety & protection

Fire Fighting · 2 items

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)

Use water spray, carbon dioxide, foam, powder.

First Aid Measures · 4 items

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .

Rinse with plenty of water for several minutes (remove contact lenses if easily possible).

Rinse mouth. Refer for medical attention .

First Aid · 1 item

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Safe StorageSeparated from strong oxidants, acids, acid anhydrides, acid chlorides, hypochlorites, halogens and food and feedstuffs. Well closed. Provision to contain effluent from fire extinguishing. Store in an area without drain or sewer access.
Fire Fighting Procedures · 2 items

USE WATER SPRAY, DRY CHEMICAL, FOAM, OR CO2. WEAR FULL PROTECTIVE CLOTHING. /XYLIDINES/

If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. /Xylidines/

Cleanup Methods · 2 items

Environmental considerations - land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, or commercial sorbents. /Xylidines/

Environmental considerations - water spill: Use natural barriers or oil spill control booms to limit spill travel. Remove trapped material with suction hoses. /Xylidines/

Toxicology

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a recommended classification scheme(1), an estimated Koc value of 240(SRC), determined from a measured log Kow of 1.84(2) and a recommended regression-derived equation(3), indicates that 3,4-xylidine will have moderate mobility in soil(SRC). However, anilines are expected to bind strongly to humus or soil organic matter in soils due to the high reactivity of the aromatic amino group(4,5), suggesting that mobility may be much lower in some soils(SRC). Volatilization of 3,4-xylidine may be important from moist soil surfaces(SRC) given a measured Henry's Law constant of 1.85X10-5 atm-cu m/mole(2). Based on limited aqueous screening study data, 3,4-xylidine may biodegrade under aerobic conditions in soil(SRC); 3,4-xylidine, present at 30 mg/l, reached 7.1% of the theoretical BOD in 4 weeks using an activated sludge inoculum(6).

AQUATIC FATE: Based on a recommended classification scheme(1), an estimated Koc value of 240(SRC), determined from a measured log Kow of 1.84(2) and a recommended regression-derived equation(1), indicates that 3,4-xylidine should not adsorb to suspended solids and sediment in water(SRC). However, aromatic amine groups are recognized as having a strong affinity to organic carbon, suggesting that this compound may bind strongly to suspended organic material in water(3,4). 3,4-Xylidine may volatilize from water surfaces(1,SRC) based on a measured Henry's Law constant of 1.85X10-5 atm-cu m/mole(2). Estimated volatilization half-lives for a model river and model lake are 2 and 21 days, respectively(1,SRC). According to a classification scheme(5), measured BCF values of 1.9-3.3 and <10(6), measured in carp, suggest that bioconcentration in aquatic organisms is low(SRC). Based on limited aqueous screening study data, 3,4-xylidine may biodegrade slowly under aerobic conditions in water(SRC); 3,4-xylidine, present at 30 mg/l, reached 7.1% of the theoretical BOD in 4 weeks using an activated sludge inoculum(6).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 3,4-xylidine, which has a measured vapor pressure of 0.028 mm Hg at 25 °C(2), should exist solely as a vapor in the ambient atmosphere. Vapor-phase 3,4-xylidine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be about 2 hours(3,SRC).

Exposure RoutesThe substance can be absorbed into the body in hazardous amounts by inhalation, through the skin and by ingestion.
Signs and Symptoms · 3 items

Dizziness. Drowsiness. Headache. Nausea.

MAY BE ABSORBED! See Ingestion.

Blue lips, fingernails and skin. Dizziness. Drowsiness. Headache. Nausea. Unconsciousness.

Effluent Concentrations3,4-Xylidine was identified at unreported concentrations in Latakia tobacco smoke and in a steam distillate of cured Latakia tobacco(1).
ICSC Environmental DataThe substance is toxic to aquatic organisms. It is strongly advised not to let the chemical enter into the environment.
Medical Surveillance · 1 item

Initial medical examination: A complete history & physical examination. The purpose is to detect existing conditions that might place the exposed employee at increased risk, and to establish a baseline for future health monitoring. Exam of the blood, lung, liver, kidneys, and cardiovascular system should be stressed. ... Periodic medical exam ... should be repeated on an annual basis. /Xylidines/

Safety data

F
8
PPE
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
wgk
2
tsca
TSCA listed
rtecs
ZE9450000
ridadr
UN 3452 6.1/PG 2

Chemistry & industry

Pharmacology

Metabolism/MetabolitesYIELDS 2-AMINO-4,5-DIMETHYLPHENOL, 3,4-DIMETHYLACETANILIDE AND 3,4-DIMETHYLPHENYLSULFAMATE IN RAT. /FROM TABLE/

Uses & manufacturing

UsesUsed as a chemical intermediate for the synthesis of riboflavin.
U.S. Imports · 2 items

(1974) 4.99X10+4 GRAMS (PRINCPL CUSTMS DISTS)

(1975) 4.99X10+4 GRAMS (PRINCPL CUSTMS DISTS)

Methods of Manufacturing · 3 items

NITRATION OF O-XYLENE FOLLOWED BY REDUCTION; BROMINATION OF O-XYLENE FOLLOWED BY REACTION WITH AMMONIA

o-Xylene (nitration/nitro reduction)

Soboley and Berezooskii patented the production of 3,4-xylidine by the hydrogenation of 2-chloromethyl-4-nitrotoluene.

General Manufacturing InformationBenzenamine, 3,4-dimethyl-: ACTIVE
Applications · 3 items

Uses3,4-Dimethylaniline is used to study electron donor-acceptor interaction with DCNQ. It is also used as a fine chemical &organic intermediate.

Uses3,4-Dimethylaniline (3,4-DMA) has been used to study the electron donor-acceptor (EDA) interaction between 2,3-dicyano-1,4-naphthoquinone (DCNQ) and 3,4-dimethylaniline, in chloroform and dichloromethane. It can also be used for reactions with MoO(X)2(dtc)2 (X = Cl or Br; dtc = diethyldithiocarbamate) in methanol to form ionic imido complexes of the type [MoNAr(dtc)3]2[Mo6O19] or MoNAr(dtc)3]4[Mo8O26].

General DescriptionPale brown crystals or off-white solid.

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Changzhou Carman Chemical Co., Ltd.15061933924
温州共赢化学有限公司+86-0086-577-64498589 +86-15355981851 · [email protected]

Additional notes

DefinitionChEBI: A primary arylamine that is aniline in which the hydrogens at the 3- and 4-positions are replaced by methyl groups. A low-melting, crystalline solid, it is used in the production of vitamin B2, dyes, pesticides and other chemicals.

Related reactions

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