5-Methyl-o-anisidin

2-Methoxy-5-Methylaniline

HCID 8445CAS 120-71-8

Grundinformationen

Standard-SMILES
COc1ccc(C)cc1N
InChIKey
WXWCDTXEKCVRRO-UHFFFAOYSA-N
Summenformel
C8H11NO
Durchschnittliche Molmasse
137,18 g/mol
Monoisotopische Masse
137,08406397

Überblick

p-Cresidine can cause cancer according to an independent committee of scientific and health experts.

Namen und Bezeichner

Bevorzugter Name
2-Methoxy-5-Methylaniline
IUPAC
2-methoxy-5-methylaniline
Lokaler Name
5-Methyl-o-anisidin
Englischer Name
2-Methoxy-5-methylaniline
Summenformel
C8H11NO
Molmasse
137.18

Namen und Synonyme

2-Methoxy-5-methylaniline120-71-8P-CRESIDINECresidine5-Methyl-o-anisidinepara-CresidineKrezidin2-Amino-4-methylanisole3-Amino-4-methoxytoluene4-Methoxy-m-toluidineKrezidine1-Amino-2-methoxy-5-methylbenzene
Weitere Namen anzeigen
PARA CRESIDINE6-METHOXY-M-TOLUIDINE6-methoxy-m-toluidine p-cresidine2-Methoxy-5-methylaniline,5-Methyl-o-anisidine, 6-Methoxy-m-toluidine, p-CresidineKresidin
4-Methyl-2-aminoanisoleAzoic Red 362-Methoxy-5-methylbenzenamineo-Anisidine, 5-methyl-C.I. Azoic Red 833-Amino-p-cresol methyl etherNCI-C02982m-Amino-p-cresol, methyl ester

Datenbank-Bezeichner

CAS
120-71-8
PubChem CID
8445
DTXSID
DTXSID1020350
ChEMBL
CHEMBL398755
ChEBI
CHEBI:82307
UNII
4C11L78UR3
EC Number
204-419-1
Nikkaji
J5.331G

Eigenschaften

Berechnete Struktureigenschaften

XLogP
1,7
Polarare Oberfläche (TPSA)
35,3 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
1
Schwere Atome
10

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Nitrogen Compounds -> Amines, Aromatic

Carcinogens

LogP · 3 Einträge

log Kow= 1.74

1.67

1.74

Density1 (NTP, 1992)
Color/FormWhite crystals
Solubility · 3 Einträge

less than 1 mg/mL at 72 °F (NTP, 1992)

Slightly soluble in water, chloroform. Soluble in ether, benzene, petroleum ether, and ethanol.

Solubility in water: poor

CorrosivityLiquid anisidine will attack some forms of plastics, rubber, and coatings. /o-Anisidine/

Physikochemische Eigenschaften

Schmelzpunkt
50 · 50-52 °C (lit.)
Siedepunkt
235 °C · 235 °C (lit.)
Dichte
1.0252 · 1.0252 (rough estimate)
Dampfdichte
4.7 · 4.7 (vs air)
Dampfdruck
2.6 Pa · 2.6Pa at 20℃
Brechungsindex
1.5647 · 1.5647 (estimate)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

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

P203, P264, P270, P280, P301+P317, P318, P330, P405, and P501 (click each P-code to see the statement)

Danger

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P203, P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P318, P330, P337+P317, P405, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 5 Einträge

Hazard Traits - Carcinogenicity

Benzenamine, 2-methoxy-5-methyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenamine, 2-methoxy-5-methyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 05-11-2010 https://echa.europa.eu/registration-dossier/-/registered-dossier/1299

Substance: 6-methoxy-m-toluidine (p-cresidine)

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Fire Hazards · 2 Einträge

This chemical is nonflammable. (NTP, 1992)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Finely dispersed particles form explosive mixtures in air.

Health Hazards · 1 Eintrag

SYMPTOMS: Symptoms of exposure to this compound may include eye and skin irritation. Other symptoms include methemoglobinemia with cyanosis (bluish discoloration of the lips, skin, earlobes and fingernails). Exposure can cause drowsiness, nausea, vomiting, weakness, somnolence, liver damage and unconsciousness.

Hazards Summary · 1 Eintrag

Possibly carcinogenic to humans; [ICSC] Irritating to the skin and eyes; [HSDB] Harmful by ingestion, inhalation, and skin absorption; Can cause methemoglobinemia, damage to the liver, and unconsciousness; [CAMEO] An eye irritant; May induce methemoglobinemia; Targets blood, liver, and bladder; [MSDSonline]

Reactive GroupEthers
EC ClassificationSymbol: T; R: 45-22; S: 53-45; Note: E

Sicherheit und Schutzausrüstung

Fire Fighting · 2 Einträge

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)

Use water spray, foam, powder, carbon dioxide.

First Aid Measures · 4 Einträge

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Refer for medical attention .

First Aid · 1 Eintrag

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 and food and feedstuffs.
Fire Fighting Procedures · 2 Einträge

Extinguishant: Foam, carbon dioxide, dry chemical. /o-Anisidine/

If material is involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Keep run-off water out of sewers and water sources. /Anisidines/

Storage Conditions · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/

Toxikologische Informationen

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 53(SRC), determined from a log Kow of 1.74(2) and a regression-derived equation(3), indicates that p-cresidine is expected to have high mobility in soil(SRC). However, aromatic amines are expected to bind strongly to humus or organic matter in suspended solids and sediments due to the high reactivity of the aromatic amino group(4,5). Volatilization of p-cresidine from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.2X10-7 atm-cu m/mole(SRC), using a fragment constant estimation method(6). p-Cresidine is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 2.5X10-2 mm Hg(SRC), determined from a fragment constant method(7). p-Cresidine reached 0.7% of its theoretical BOD in 2 weeks using the Japanese MITI test(8), suggesting that biodegradation is not a rapid environmental fate process in soils(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 53(SRC), determined from a log Kow of 1.74(2) and a regression-derived equation(3), indicates that p-cresidine is not expected to adsorb to suspended solids and sediment(SRC). However, aromatic amines are expected to bind strongly to humus or organic matter in suspended solids and sediments due to the high reactivity of the aromatic amino group(4,5). Volatilization from water surfaces may occur slowly(3) based upon an estimated Henry's Law constant of 1.2X10-7 atm-cu m/mole(SRC), developed using a fragment constant estimation method(6). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 23 and 169 days, respectively(SRC). According to a classification scheme(7), a BCF of <4.6(8), suggests bioconcentration in aquatic organisms is low(SRC). p-Cresidine reached 0.7% of its theoretical BOD in 2 weeks using the Japanese MITI test(8), suggesting that biodegradation is not a fast environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), p-cresidine, which has an estimated vapor pressure of 2.5X10-2 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase p-cresidine 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 2 hrs(SRC), calculated from its rate constant of 2.2X10-10 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3).

Adverse EffectsOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Exposure RoutesThe substance can be absorbed into the body by inhalation and by ingestion.
Signs and Symptoms · 2 Einträge

Cough.

Redness.

Ongoing Test Status · 1 Eintrag

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=120-71-8]

Medical Surveillance · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Whenever medical surveillance is indicated, in particular when exposure to a carcinogen has occurred, ad hoc decisions should be taken concerning ... /cytogenetic and/or other/ tests that might become useful or mandatory. /Chemical Carcinogens/

Sicherheitsdaten

F
9
wgk
3
tsca
TSCA listed
hs_code
29222990
RTECS-Nr.
BZ6720000
risk_code
45-22

Chemie und Industrie

Verwendung und Herstellung

Uses · 4 Einträge

Chemical intermediate for dyes; [HSDB]

For p-cresidine (USEPA/OPP Pesticide Code: 042002) there are 0 labels match. /SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Chem int for dyes (e.g., FD&C Red 40 and Direct Violet 9)

Substance listed with specific concentration in tattoo ink and/or permanent make up according to EU Commission Regulation 2020/2081. The concentration limit (by weight) is 0.0005%.

U.S. Imports · 2 Einträge

(1977) 4.02X10+7 GRAMS (PRINCPL CUSTMS DISTS)

(1979) 2.67X10+8 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 2 Einträge

2023: 6,613 lb

(1977) 4.54X10+7 - 4.54X10+8 GRAMS

Consumption PatternsESSENTIALLY 100% AS A CHEMICAL INTERMEDIATE FOR DYES
Consumer UsesIntermediate
Industry UsesDye
Anwendungen · 1 Eintrag

Verwenden2-Methoxy-5-methylaniline was used in the synthesis of 4-(4-Amino-5-methoxy-2-methylphenylazo)-5-hydroxy-naphthalene-2,7-disulfonic acid. 2-Methoxy-5-methylaniline was used to analyse the application of polymeric ionic liquids as selective solid-phase microextraction sorbent coatings for the analysis of genotoxic impurities and structurally alerting compounds such as alkyl halides and aromatics. 2-Methoxy-5-methylaniline was used in a study to develop a sensitive analytical method for the determination of aromatic amines found in commercial hair dyes using high liquid chromatography coupled to an electrochemical detector by using the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide in the mobile phase.

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