Name | 4-methyl-2-aminoanisole |
Synonyms | Cresidine krezidine azoic red NCI-C02982 p-Cresidine Para-Cresidine C.I. Azoic Red 83 5-Methyl-o-Anisidine o-Anisidine, 5-methyl- 4-methyl-2-aminoanisole 2-Methoxy-5-methylaniline 4-methoxy-3-methylaniline o-anisidine,5-methyl-(8ci) 2-Amino-p-cresolmethylether m-amino-p-cresol,methylester 2-Amino-p-cresol methyl ether 2-Amino-4-methylphenolmethylether meta-amino-para-cresol,methylether |
CAS | 120-71-8 |
EINECS | 204-419-1 |
InChI | InChI=1/C8H11NO/c1-6-5-7(9)3-4-8(6)10-2/h3-5H,9H2,1-2H3 |
InChIKey | WXWCDTXEKCVRRO-UHFFFAOYSA-N |
Molecular Formula | C8H11NO |
Molar Mass | 137.18 |
Density | 1.0252 (rough estimate) |
Melting Point | 50-52 °C (lit.) |
Boling Point | 235 °C (lit.) |
Flash Point | >230°F |
Water Solubility | Slightly soluble in hot water. |
Solubility | Chloroform (Slightly), Ethyl Acetate, Methanol (Slightly) |
Vapor Presure | 2.6Pa at 20℃ |
Vapor Density | 4.7 (vs air) |
Appearance | Crystalline Chunks |
Color | Brown to black |
BRN | 637071 |
pKa | 4.66±0.10(Predicted) |
Storage Condition | Room Temperature, under inert atmosphere |
Stability | Air Sensitive |
Refractive Index | 1.5647 (estimate) |
Physical and Chemical Properties | trait light red crystals. soluble in ethanol, ether and hydrochloric acid. <0.1g/100 mL at 22 C in waterMelting Point: 53 °c Boiling Point: 235 ℃ flash point: 110 ℃ |
Use | Suitable for the synthesis of direct, disperse and reactive dyes |
Risk Codes | R45 - May cause cancer R22 - Harmful if swallowed |
Safety Description | S53 - Avoid exposure - obtain special instructions before use. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
WGK Germany | 3 |
RTECS | BZ6720000 |
FLUKA BRAND F CODES | 9 |
HS Code | 29222990 |
Hazard Class | IRRITANT |
Raw Materials | Sodium sulfide Dimethyl sulfate Sodium hydroxide |
Downstream Products | 4-amino-5-methoxytoluene-2-sulphonic acid Direct Grey D |
white crystals. Melting point 51.5 °c, boiling point 235 °c. Insoluble in water, soluble in alcohol, ether, insoluble in benzene.
This product is a dye intermediate. It is used in the synthesis of C.I. I.29050, 29065, 27885, etc. In the case of acid dyes for the synthesis of c. I .14940, 14965, etc.
LogP | 1.65 at 23℃ and pH7 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
(IARC) carcinogen classification | 2B (Vol. 27, Sup 7) 1987 |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Application | suitable for synthesis of direct, disperse and reactive dyes This product is a dye intermediate. In terms of direct dyes for the synthesis of C. 29050, 29065, 27885, etc., in terms of acid dyes for the synthesis of C. 14940, 14965, etc., are also used in the manufacture of dispersed red GC, direct Fast Blue 3RLL, direct black D, active yellow brown K-GR, cationic Yellow 4G, etc. 3-amino-p-methylanisole is a dye intermediate. In terms of direct dyes for the synthesis of C.I.29050;29065;27885, et al., in terms of acid dyes for the synthesis C.I.14940;14965, et al., also used in the manufacture of disperse scarlet GC; Direct sunfast blue 3RLL; Direct black D; Active yellow brown K-GR; Cationic Yellow 4G, etc. This product is a kind of dye intermediate. In terms of direct dyes for the synthesis of C.I.29050;29065;27885, et al., in terms of acid dyes for the synthesis C.I.14940;14965, et al., also used in the manufacture of disperse scarlet GC; Direct sunfast blue 3RLL; Direct black D; Active yellow brown K-GR; Cationic Yellow 4G, etc. |
production method | 1. It is obtained by nitration, methoxylation and reduction of P-chlorotoluene. The mixed acid was added to p-chlorotoluene at 15-20 ℃, stirred at 30 ℃ for 2H, diluted with water, and the waste acid was separated and washed with water to obtain 4-chloro-3-nitrotoluene (yield: 30.6%). And 4-chloro-2-nitrotoluene (yield 56.7%), which were separated by fractional distillation and crystallization to give 4-chloro-3-nitrotoluene. It was reacted with methanol and sodium methoxide solution, and neutralized with sulfuric acid to give 3-nitro-4-methoxytoluene in 85.6% yield. After reduction with water, iron powder and formic acid, the solvent gasoline is extracted and distilled several times. 2. 2-nitro-4-cresol was obtained by nitration of p-cresol, then methylated with dimethyl sulfate to 3-nitro-4-p-methoxytoluene, and finally reduced with sulfide base. P-chloro-N,N-diethylbenzylamine was prepared by nitration, methoxylation and reduction. |
category | toxic substances |
toxicity grade | poisoning |
Acute toxicity | oral-rat LD50: 1450 mg/kg |
stimulation data | Skin-rabbits 500 mg/24 h mild; eye-rabbit 100 mg/24 h moderate |
flammability hazard characteristics | open flame flammable; Toxic aniline gas emitted by heat |
storage and transportation characteristics | The warehouse is ventilated and dried at low temperature; It is stored and transported separately from food raw materials |
fire extinguishing agent | water, carbon dioxide, sand, dry powder |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |