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Home > Encyclopedia > 4-Nitrophthalic anhydride

4-Nitrophthalic anhydride

4-Nitrophthalic anhydride structure

4-Nitrophthalic anhydride 

structure
  • CAS No:

    5466-84-2

  • Formula:

    C8H3NO5

  • Chemical Name:

    4-Nitrophthalic anhydride

  • Synonyms:

    1,3-Isobenzofurandione,5-nitro-;Phthalic anhydride,4-nitro-;5-Nitro-1,3-isobenzofurandione;4-Nitrophthalic anhydride;4-Nitrophthalic acid anhydride;5-Nitrophthalic anhydride;5-Nitroisobenzofuran-1,3-dione;NSC 26424

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

off-white to light yellow-brown powder


4-nitrophthalic anhydride is a yellow powder. (NTP, 1992)


4-nitrophthalic anhydride is a yellow powder. (NTP, 1992)

4-Nitrophthalic anhydride Basic Attributes

193.11

193.11

179682

226-776-2

SQN32UA63N

26424

DTXSID6025775

29173990

Characteristics

89.2

1.1

4-nitrophthalic anhydride is a yellow powder. (NTP, 1992)

1.441 g/cm3 @ Temp: 25.00 °C

114 °C

197 °C / 8mmHg

227.5ºC

1.585

Hydrolysis

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture.

Reacts with water. The organic acids produced by this reaction are significantly more soluble in water.

Nitro, Nitroso, Nitrate, and Nitrite Compounds, Organic

Water-Reactive

4-NITROPHTHALIC ANHYDRIDE reacts exothermically with water. The reactions are usually slow, but might become violent if local heating accelerates their rate. Acids accelerate the reaction with water. Incompatible with acids, strong oxidizing agents, alcohols, amines, and bases.

Safety Information

3

36/37/38-20/22

26-36-36/37/39-22

TI3328000

Xi,Xn

Stable at room temperature in closed containers under normal storage and handling conditions.

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

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

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 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 store this material in a refrigerator. (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

SYMPTOMS: Symptoms of exposure to this compound include coughing, sneezing, burning in respiratory system, dermatitis, and skin irritation. Symptoms of chronic exposure include bronchitis, eye irritation, inflammation of respiratory tract and bloody nasal discharge. ACUTE/CHRONIC HAZARDS: This compound may cause severe skin and eye irritation. It may also cause mucous membrane irritation. (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-Nitrophthalic anhydride Use and Manufacturing

Methods of Manufacturing

From 4-nitrophthalimide hydrolysis to generate 4-nitrophthalic acid (610-27-5), and then obtained by dehydration. Add 4-nitrophthalimide to the sodium hydroxide solution and heat to boil for 15 min. Adjust pH 6-8 with nitric acid, then add nitric acid and boil for 5 min. After cooling, filtering, the filtrate was extracted with diethyl ether. After the extract was dried, the diethyl ether was distilled off to precipitate 4-nitrophthalic anhydride crystals. The yield is 95%.

Uses

5-Nitrophthalic Anhydride is used in the preparation of phthalic acids as well as compounds with anticonvulsant activities.

1,3-Isobenzofurandione, 5-nitro-: ACTIVE

Computed Properties

Molecular Weight:193.11
XLogP3:1.1
Hydrogen Bond Acceptor Count:5
Exact Mass:193.00112220
Monoisotopic Mass:193.00112220
Topological Polar Surface Area:89.2
Heavy Atom Count:14
Complexity:307
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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