HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Compound

3,4-Dimethylaniline

HCID 7248
New noteNew reactionRequest quotes
Print preview

Completing data — refresh the page later to see the latest

Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
95-64-7
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 propertiesFilling in

XLogP
2.5
Topological polar surface area
26 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
9
Formal charge
0
Complexity
90.6

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

Flash Point · 2 items

209 °F (NTP, 1992)

98 °C

Boiling Point · 3 items

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

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

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.

Upstream & downstream products

Related reactions

139 records
New reaction record
HRID 2443 reaction equation
HRID 2443As reactantuspto-grants-1998_03
HRID 3023 reaction equation
HRID 3023As reactantuspto-grants-1998_03
HRID 3717 reaction equation
HRID 3717As reactantuspto-grants-1998_03
HRID 46648 reaction equation
HRID 46648As reactantuspto-grants-1979_11
HRID 58597 reaction equation
HRID 58597As reactantuspto-grants-2016_09
HRID 96483 reaction equation
HRID 96483As reactantTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 99053 reaction equation
HRID 99053As reactantTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 100992 reaction equation
HRID 100992As reactantTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Page 1 of 18

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
More actions
New noteNew reactionRequest quotes

442 °F at 760 mmHg (NTP, 1992)

228 °C @ 760 MM HG

228 °C

DecompositionWHEN HEATED TO DECOMP, XYLIDINES EMIT HIGHLY TOXIC FUMES. /XYLIDINES/
Melting Point · 3 items

124 °F (NTP, 1992)

51 °C

51 °C

Vapor DensityRelative vapor density (air = 1): 4.19
Odor Threshold · 2 items

Odor threshold in air= 1.00X10+12 molecules/cc /Xylidines/

Threshold for xylidine is 0.0240 mg/cu m. /Xylidine/

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
storage temp.
30 °C · Store below +30°C.
solubility
0.1 g/mL, · methanol: 0.1 g/mL, clear
pka
1 · pK1:5.17(+1) (25°C)
form
Crystalline Mass or Crystals
color
Light beige to pink to brown
Water Solubility
1 g/L · <1 g/L (24 ºC)
Merck
14 · 14,10084
BRN
507414 · 507414
Henry's Law Constant
5.3 · 5.3×100 mol/(m3Pa) at 25℃, Jayasinghe et al. (1992)
InChI
1S/C8H11N/c1-6-3-4-8(9)5-7(6)2/h3-5H,9H2,1-2H3
InChIKey
DOLQYFPDPKPQSS-UHFFFAOYSA-N
SMILES
Cc1ccc(N)cc1C
LogP
1.8 at · 1.8 at 25℃
Dissociation constant
5.15 at · 5.15 at 25℃
CAS DataBase Reference
95 · 95-64-7(CAS DataBase Reference)
EWG's Food Scores
1 · 1
FDA UNII
27 I33AIDT · R27I33AIDT
NIST Chemistry Reference
3 · Benzenamine, 3,4-dimethyl-(95-64-7)
EPA Substance Registry System
3 · 3,4-Dimethylaniline (95-64-7)
UNSPSC Code
12352100 · 12352100
NACRES
22 · NA.22
Symbol(GHS)
7 · GHS07,GHS08,GHS09
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H373-H335-H411
Precautionary statements
501 · P501-P273-P260-P270-P271-P264-P280-P302+P352-P391-P314-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P304+P340+P312-P403+P233-P405
PPE
95 · dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes
T,N
Risk Statements
23 · 23/24/25-33-51/53
Safety Statements
28 · 28-36/37-45-61-28A
RIDADR
3452 · UN 3452 6.1/PG 2
WGK Germany
2 · 2
RTECS
9450000 · ZE9450000
F
8 · 8
TSCA
TSCA listed
HazardClass
6.1 · 6.1
PackingGroup
II
HS Code
29214910 · 29214910
Storage Class
6.1 A · 6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
Hazard Classifications
3 DermalAcute · Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralAquatic Chronic 2STOT RE 2
Hazardous Substances Data
95 · 95-64-7(Hazardous Substances Data)
REACH Registrations
Inactive

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.

Reactive GroupAmines, Aromatic
EC ClassificationSymbol: T, N; R: 23/24/25-33-51/53; S: (1/2)-28-36/37-45-61; Note: C
UN ClassificationUN Hazard Class: 6.1; UN Pack Group: II
OSHA Standards · 2 items

Permissible Exposure Limit: Table Z-1 8-hr Time-Weighted Avg: 5 ppm (25 mg/cu m). Skin Designation. /Xylidine/

Vacated 1989 OSHA PEL TWA 2 ppm (10 mg/cu m), skin designation, is still enforced in some states. /Xylidine/

Reactivity Profile · 1 item

3,4-XYLIDINE ignites on contact with fuming nitric acid (NTP, 1992). Neutralizes acids in 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 may be generated in combination with strong reducing agents, such as hydrides.

Chemical Dangers · 1 item

Decomposes on burning. This produces toxic and corrosive fumes including nitrogen oxides. Reacts violently with strong oxidants. Reacts with hypochlorites. This produces explosive chloroamines. Reacts with acids, acid anhydrides, acid chlorides and halogens. Attacks plastic and rubber.

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/

Nonfire Spill Response · 1 item

SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 2 items

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Disposal methods: incineration. A). Dissolve in such combustible solvent as alcohols, benzene, etc. Spray solvent into the furnace with afterburner and scrubber. B). Pour into a mixture of sand and soda ash (9:1). After mixing, put into a paper carton stuffed full with packing paper to serve as fuel. Burn in the furnace. /Xylidines/

Spillage Disposal · 1 item

Personal protection: chemical protection suit and filter respirator for organic gases and particulates adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers.

Preventive Measures · 5 items

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Non-impervious clothing which becomes contaminated with xylidine should be removed immediately and not reworn until the xylidine is removed from the clothing. /Xylidines/

Eating and smoking should not be permitted in areas where liquid xylidine is handled, processed, or stored. /Xylidines/

Employees who handle liquid xylidine should wash their hands thoroughly with soap or mild detergent and water before eating, smoking, or using toilet facilities. /Xylidines/

For more Preventive Measures (Complete) data for 3,4-XYLIDINE (7 total), please visit the HSDB record page.

Isolation and EvacuationExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Eye PreventionWear safety spectacles or eye protection in combination with breathing protection.

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/

Soil Adsorption/Mobility · 1 item

The Koc of 3,4-xylidine is estimated as approximately 240(SRC), using a measured log Kow of 1.84(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that 3,4-xylidine has moderate mobility in soil(SRC). However, anilines are expected to bind stongly to humus or soil organic matter in soils due to the high reactivity of the aromatic amino group(4,5). Low adsorption is observed at a neutral pH with pure clay minerals or soils for substituted anilines(5).

Artificial Pollution Sources3,4-Xylidine's production and use in the manufacture of synthetic riboflavin(1) may result in its release to the environment through various waste streams(SRC).
Environmental Biodegradation · 1 item

3,4-Xylidine, present at 30 mg/l, reached 7.1% of the theoretical BOD in 4 weeks using an activated sludge inoculum(1). In the Japanese MITI test, 3,4-xylidine (present at 100 mg/l) was classified as slow to biodegrade indicating that only 0-29% of the theoretical BOD was reached in 2 weeks using an activated sludge inoculum(2). 3,4-Xylidine, present initially at 252 mg/L, was removed at a biodegradation rate of 30 mg COD/g-hr by an activated sludge inoculum(3). E.coli converted 3,4-xylidine to the corresponding (phenylazo)naphthol in the presence of nitrate with this reaction proceeding within 24 hours(4).

Environmental Bioconcentration · 1 item

BCF values of 1.9-3.3 and <10 were measured in carp for 3,4-xylidine at 1 and 0.1 mg/l, respectively, using a flow through system(1). According to a classification scheme(3), these BCF values suggest that bioconcentration in aquatic organisms is low(SRC).

Volatilization from Water/Soil · 1 item

A Henry's Law constant of 1.85X10-5 atm-cu m/mole was measured for 3,4-xylidine(1). This value indicates that 3,4-xylidine will volatilize from water surfaces(2,SRC). Based on this Henry's Law constant, the estimated volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) is estimated as approximately 2 days(2,SRC). The estimated volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as approximately 21 days(2,SRC) although adsorption to organic material in water may attenuate this process(SRC). 3,4-Xylidine's Henry's Law constant(1,SRC) indicates that volatilization from moist soil surfaces may occur(SRC).

Non-Human Toxicity Excerpts · 5 items

... 3,4-DIMETHYLANILINE ... CARCINOGENIC, BECAUSE ... /IT/ INDUCED PITUITARY ADENOMAS IN BUFFALO RATS.

3,4-DIMETHYLANILINE WAS TESTED FOR ITS ABILITY TO MUTATE SALMONELLA TYPHIMURIUM & WAS FOUND TO BE WEAKLY MUTAGENIC (LESS THAN 150 REVERTANTS/UMOLE).

THE ORAL LD50 VALUES IN RATS FOR DI-SUBSTITUTED ANILINES INCR COMPARED TO MONO-SUBSTITUTED ANILINES. /SUBSTITUTED ANILINES/

In the Rec-assay using Bacillus subtillis, the 2,3-, 2,5-, 2,6-, 3,4-, and 3,5-isomers were negative; 2,4-xylidine was positive.

For more Non-Human Toxicity Excerpts (Complete) data for 3,4-XYLIDINE (6 total), please visit the HSDB record page.

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
hs_code
29214910
risk_code
23/24/25-33-51/53
Signal word
Warning
Symbol(GHS)
GHS07,GHS08,GHS09
hazard_code
T,N
safety_code
28-36/37-45-61-28A
hazard_class
6.1
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
packing_group
II
Hazard statements
H302-H315-H319-H373-H335-H411
REACH Registrations
Inactive
Hazard Classifications
Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralAquatic Chronic 2STOT RE 2
Precautionary statements
P501-P273-P260-P270-P271-P264-P280-P302+P352-P391-P314-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P304+P340+P312-P403+P233-P405
Hazardous Substances Data
95-64-7(Hazardous Substances Data)

Upstream raw materials

o-XyleneChloroacetic acid3',4'-DimethylacetophenoneAluminum chloride4-Nitrotoluenepolyphosphoric acidSodium cyanideHydrochloric acidHydrogenBis(chloromethyl)etherHydroxylamine hydrochloridePotassium AcetateIsopropyl alcoholSulfuric acid

Downstream products

Vitamin B22,3-Dihydroxy-6,7-dimethylquinoxaline2-Amino-5,6-dimethylbenzothiazole4,6-Dimethyl-1,2-phenylenediamineRiboflavinPendimethalin4,5-Dimethyl-2-nitroaniline2,5-Dimethylaniline3,4-Dimethylbenzoic acid4-Chloro-6,7-dimethylquinoline1,2-Dimethyl-4-fluorobenzene

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.