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Home > Encyclopedia > 4-(2-Naphthalenylamino)phenol

4-(2-Naphthalenylamino)phenol

4-(2-Naphthalenylamino)phenol structure

4-(2-Naphthalenylamino)phenol 

structure
  • CAS No:

    93-45-8

  • Formula:

    C16H13NO

  • Chemical Name:

    4-(2-Naphthalenylamino)phenol

  • Synonyms:

    Phenol,4-(2-naphthalenylamino)-;Phenol,p-(2-naphthylamino)-;4-(2-Naphthalenylamino)phenol;p-Hydroxyphenyl-β-naphthylamine;p-Hydroxyphenyl-2-naphthylamine;p-Hydroxyneozon;N-(p-Hydroxyphenyl)-β-naphthylamine;p-(β-Naphthylamino)phenol;p-Hydroxyneozone;p-(2-Naphthylamino)phenol;Paraoxyneozone;4-Hydroxyphenyl-β-naphthylamine;N-(p-Hydroxyphenyl)-2-naphthylamine;4-(2-Naphthylamino)phenol;N-(4-Hydroxyphenyl)-2-naphthylamine;NSC 15372;NSC 21065;2-(4-Hydroxyphenylamino)-naphthalene

  • Categories:

    Dyes and Pigments  >  Dye

Description

purple solid


4-(2-naphthylamino)phenol is a purple solid. (NTP, 1992)


4-(2-naphthylamino)phenol is a purple solid. (NTP, 1992)

4-(2-Naphthalenylamino)phenol Basic Attributes

235.28052

235.28

202-248-7

391R4KT1XJ

21065|15372

DTXSID8025701

2922299090

Characteristics

32.26000

4.05

4-(2-naphthylamino)phenol is a purple solid. (NTP, 1992)

1.3±0.1 g/cm3

140 °C

250 °C @ Press: 4 Torr

173.1±12.4 °C

1.734

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

This chemical may be sensitive to prolonged exposure to air. Insoluble in water.

Amines, Phosphines, and Pyridines

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 pKa = 9.88). 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.

Safety Information

20/21/22-36/37/38-40

26-36/37/39-45

SM1750000

Xn

Stable. Incompatible with strong oxidizing agents.

P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P312, P304+P340, P305+P351+P338, P308+P313, P312, P321, P322, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501

H312

Flash point data for this compound are not available, however, it is probably combustible. (NTP, 1992)

|Warning|H312 (97.44%): Harmful in contact with skin [Warning Acute toxicity, dermal]|P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P312, P304+P340, P305+P351+P338, P308+P313, P312, P321, P322, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Fires involving this compound can be controlled using a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)

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. STORAGE PRECAUTIONS: You should keep this material in a tightly-closed container under an inert atmosphere, and store it at refrigerated temperatures. (NTP, 1992)

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Drug Information

ACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits toxic fumes. (NTP, 1992)

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. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

4-(2-Naphthalenylamino)phenol Use and Manufacturing

Methods of Manufacturing

Derived by condensation of 2-naphthol and p-aminophenol. First add 150kg 2-naphthol to the reaction pot, then add 75kg p-aminophenol, and then cover 30kg 2-naphthol on the surface (to prevent oxidation). Cover and dehydrate at 100°C (74.7-77.3kPa) for 1h. Condensation is carried out at 74.48kPa, and the temperature is raised to 180-190℃ by the heat of reaction; then the temperature gradually drops to 150-160℃ within 3h. Reduce pressure to 1.33-2.67kPa. Heat to 190°C and distill off 2-naphthol until the outlet temperature drops to 140-150°C. Press the material with compressed air and cool it in the pan to obtain N-(p-hydroxyphenyl)-2-naphthylamine.

Uses

Used for dyeing cotton and Uygur/cotton blended fabrics

Phenol, 4-(2-naphthalenylamino)-: INACTIVE

Computed Properties

Molecular Weight:235.28
XLogP3:4.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:235.099714038
Monoisotopic Mass:235.099714038
Topological Polar Surface Area:32.3
Heavy Atom Count:18
Complexity:260
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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