Molecular Structure of 3-Ethylamino-4-methylphenol (CAS NO.120-37-6):

IUPAC Name: 3-(ethylamino)-4-methylphenol
Molecular formula: C₉H₁₃NO
Molecular Weight: 151.21
Density: 1.079 g/cm³
Boiling point: 294.4 ^°C at 760 mmHg
Flash point: 139.7 ^°C
BRN: 3241548
Index of Refraction:1.588
Molar Refractivity:47.2 cm³
Molar Volume:140.1 cm³
Polarizability: 18.71*10^-24cm³
Surface Tension: 42.9 dyne/cm
Enthalpy of Vaporization: 55.54 kJ/mol
Vapour Pressure: 0.000927 mmHg at 25^°C
Melting point: 85-87 °C(lit.)
Appearance: purple solid
Stability: Stable.Incompatible with strong oxidizing agents.
InChI
InChI=1/C9H13NO/c1-3-10-9-6-8(11)5-4-7(9)2/h4-6,10-11H,3H2,1-2H3
Smiles
c1(c(ccc(c1)O)C)NCC
Classification Code: Mutation data
EINECS: 204-391-0
Product Categories: Intermediates of Dyes and Pigments; Organic Building Blocks; Oxygen Compounds; Phenols

Reported in EPA TSCA Inventory.

Mutation data reported. When heated to decomposition it emits toxic vapors of NO_x.
Hazard Codes: Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S37/39:Wear suitable gloves and eye/face protection.
WGK Germany: 2
RTECS: SL4105000

  3-Ethylamino-4-methylphenol , with CAS number of 120-37-6, can be called Phenol, 3-(ethylamino)-4-methyl- ; 3-(Ethylamino)-p-cresol ; 3-ethylamino-p-cresol ; 3-ethylamino-4-methyl-phenol . It is a purple solid. 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. It is mainly used as dye intermediates.