Welcome to LookChem.com Sign In|Join Free

CAS

  • or

120-37-6

Post Buying Request

120-37-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

120-37-6 Usage

Chemical Properties

purple solid

Uses

3-Ethylamino-4-methylphenol was used in the synthesis of rhodol by undergoing condensation reaction with 2-(2,4-dihydroxybenzoyl)benzoic acid.

General Description

Purple solid.

Air & Water Reactions

3-Ethylamino-4-methylphenol may be sensitive to prolonged exposure to air. . Insoluble in water.

Reactivity Profile

An amine and phenol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

Fire Hazard

Flash point data for 3-Ethylamino-4-methylphenol are not available. 3-Ethylamino-4-methylphenol is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 120-37-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120-37:
(5*1)+(4*2)+(3*0)+(2*3)+(1*7)=26
26 % 10 = 6
So 120-37-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-3-10-8-6-7(2)4-5-9(8)11/h4-6,10-11H,3H2,1-2H3

120-37-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 5g

  • 384.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 25g

  • 1450.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 5g

  • 384.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 25g

  • 1450.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 5g

  • 384.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 25g

  • 1450.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 5g

  • 384.0CNY

  • Detail
  • Alfa Aesar

  • (L12768)  3-Ethylamino-4-methylphenol, tech. 90%   

  • 120-37-6

  • 25g

  • 1450.0CNY

  • Detail

120-37-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethylamino-4-methylphenol

1.2 Other means of identification

Product number -
Other names 3-EthylaMino-4-Methylphenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120-37-6 SDS

120-37-6Synthetic route

3-(ethylamino)-4-methylbenzenesulfonic acid
98-40-8

3-(ethylamino)-4-methylbenzenesulfonic acid

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

Conditions
ConditionsYield
Stage #1: 3-(ethylamino)-4-methylbenzenesulfonic acid With water; potassium hydroxide at 240℃; for 75h;
Stage #2: With hydrogenchloride In water at 40℃; Temperature;
75%
2-ethylamino-toluenesulfonic acid-(4)-sodium salt

2-ethylamino-toluenesulfonic acid-(4)-sodium salt

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

Conditions
ConditionsYield
With potassium hydroxide at 220 - 260℃; beim Verschmelzen;
C16H19N3O2

C16H19N3O2

A

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

B

3-amino-4-hydroxytoluene
95-84-1

3-amino-4-hydroxytoluene

Conditions
ConditionsYield
With sodium dithionite In acetone at 37℃; for 0.25h; pH=7.4;
o-toluidine
95-53-4

o-toluidine

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: sulfuric acid; Al2O3/Fe3O4 / 3 h / 70 °C / pH 2.5 / Inert atmosphere; Large scale
2.1: sulfuric acid / 6 h / 50 - 65 °C / Large scale
3.1: potassium hydroxide; water / 75 h / 240 °C
3.2: 40 °C
View Scheme
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

3-amino-4-hydroxytoluene
95-84-1

3-amino-4-hydroxytoluene

C16H19N3O2

C16H19N3O2

Conditions
ConditionsYield
Stage #1: 3-amino-4-hydroxytoluene With hydrogenchloride; sodium nitrite In water at 0℃; for 0.25h;
Stage #2: With aminosulfonic acid for 0.0833333h; pH=9; Cooling with ice;
Stage #3: 3-ethylamino-4-methylphenol at 0 - 20℃; for 0.666667h; Time;
100%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

N-ethyl-5-hydroxy-2-methyl-4-nitrosobenzenaminium chloride

N-ethyl-5-hydroxy-2-methyl-4-nitrosobenzenaminium chloride

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite for 1h; cooling;90%
With sodium nitrite
With sodium nitrite Acidic aq. solution;
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

acetic anhydride
108-24-7

acetic anhydride

N-ethyl-N-(5-hydroxy-2-methylphenyl)acetamide

N-ethyl-N-(5-hydroxy-2-methylphenyl)acetamide

Conditions
ConditionsYield
In water at 20℃; Sonication; Heating;85%
In water at 20 - 50℃; Sonication;85%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

5-ethylamino-4-methyl-2-nitrosophenol hydrochloride
63549-31-5

5-ethylamino-4-methyl-2-nitrosophenol hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite In water at 5℃; for 3h;79%
With hydrogenchloride; sodium nitrite In water at 0 - 5℃; for 3h;79%
With sodium nitrite acidic solution;
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

3-amino-4-methylphenol
2836-00-2

3-amino-4-methylphenol

Conditions
ConditionsYield
With piperidine; dichloro(dimethylglyoxime)(dimethylglyoximato)cobalt(III); (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate In acetonitrile at -78℃; for 24h; Reagent/catalyst; Sealed tube; Inert atmosphere; Irradiation;73%
5-diethylamino-2-nitrosophenol
6358-20-9

5-diethylamino-2-nitrosophenol

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

N-ethyl-N-(7-(ethylamino)-8-methyl-3H-phenoxazin-3-ylidene)ethanaminium

N-ethyl-N-(7-(ethylamino)-8-methyl-3H-phenoxazin-3-ylidene)ethanaminium

Conditions
ConditionsYield
With perchloric acid In water; isopropyl alcohol72%
With perchloric acid In water; isopropyl alcohol at 80℃;72%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

diethyl 2-ethoxymethylenemalonate
87-13-8

diethyl 2-ethoxymethylenemalonate

7-(ethylamino)-6-methyl-2-oxo-2H-chromene-3-carboxylate
84165-77-5

7-(ethylamino)-6-methyl-2-oxo-2H-chromene-3-carboxylate

Conditions
ConditionsYield
With titanium tetrachloride In tetrahydrofuran Heating;67%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

(E)-N-ethyl-2-fluoro-5-methoxy-4-((4-nitrophenyl)diazenyl)aniline

(E)-N-ethyl-2-fluoro-5-methoxy-4-((4-nitrophenyl)diazenyl)aniline

(Z)-N-(7-(ethylamino)-8-fluoro-2-methyl-3H-phenoxazin-3-ylidene)ethanaminium

(Z)-N-(7-(ethylamino)-8-fluoro-2-methyl-3H-phenoxazin-3-ylidene)ethanaminium

Conditions
ConditionsYield
With perchloric acid In water; isopropyl alcohol at 80℃;66%
With perchloric acid In water; isopropyl alcohol at 80℃;66%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

7-methoxy-2,2,4-trimethyl-6-nitroso-1,2-dihydroquinoline

7-methoxy-2,2,4-trimethyl-6-nitroso-1,2-dihydroquinoline

(Z)-N-(2,2,4,8-tetramethyl-1,2-dihydro-9H-pyrido[3,2-b]phenoxazin-9-ylidene)ethanaminium

(Z)-N-(2,2,4,8-tetramethyl-1,2-dihydro-9H-pyrido[3,2-b]phenoxazin-9-ylidene)ethanaminium

Conditions
ConditionsYield
With perchloric acid In water; isopropyl alcohol at 80℃;66%
With perchloric acid In water; isopropyl alcohol at 80℃;66%
3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

4-methyl-2-nitroso-5-(propylamino)phenol

4-methyl-2-nitroso-5-(propylamino)phenol

(Z)-N-(2,8-dimethyl-7-(propylamino)-3H-phenoxazin-3-ylidene)ethanaminium

(Z)-N-(2,8-dimethyl-7-(propylamino)-3H-phenoxazin-3-ylidene)ethanaminium

Conditions
ConditionsYield
With perchloric acid In water; isopropyl alcohol at 80℃;65%
With perchloric acid In water; isopropyl alcohol at 80℃;65%
C19H19NO7S2
1629670-53-6

C19H19NO7S2

3-ethylamino-4-methylphenol
120-37-6

3-ethylamino-4-methylphenol

trifluoroacetic acid
76-05-1

trifluoroacetic acid

C28H29N2O7S2(1+)*C2F3O2(1-)

C28H29N2O7S2(1+)*C2F3O2(1-)

Conditions
ConditionsYield
Stage #1: C19H19NO7S2; 3-ethylamino-4-methylphenol In methanesulfonic acid at 150℃;
Stage #2: trifluoroacetic acid In water; acetonitrile pH=2.2;
52%

120-37-6Relevant articles and documents

Production process of alkaline red intermediate 3-ethylamino-p-methylphenol

-

Paragraph 0060; 0065-0069, (2021/03/31)

The invention relates to a production process of an alkaline red intermediate 3-ethylamino p-methylphenol. The production process specifically comprises the following steps: step 1, an alkylation reaction: carrying out alkylation reaction on o-toluidine and absolute ethyl alcohol under the action of a catalyst magnetic solid acid to generate an alkylate mixture; and then rectifying the alkylate mixture to obtain the N-ethyl o-toluidine; wherein the reaction temperature of the alkylation reaction is 60-120 DEG C; wherein the addition amount of the magnetic solid acid is 4-6% of the mass ratio of the feed liquid; step 2, a sulfonation reaction: carrying out sulfonation reaction on the N-ethyl o-toluidine and fuming sulfuric acid to generate 3ethylamino-p-toluenesulfonic acid; step 3, a hydroxylation reaction: carrying out hydroxylation reaction on 3ethylamino p-toluenesulfonic acid and potassium hydroxide to generate 3-ethylamino p-methylphenol potassium salt; and step 4, acid precipitation: reacting the 3-ethylamino p-methylphenol potassium salt with hydrochloric acid to prepare the 3-ethylamino p-methylphenol. The production process is high in yield and short in reaction time.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 120-37-6