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Citraconic anhydride

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CAS:616-02-4
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  • Citraconic anhydride
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  • $1.00 / 1kg
  • 2026-03-06
  • CAS:616-02-4
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  • Purity: 99%
  • Supply Ability: 10 mt
  • Citraconic anhydride
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  • 2026-03-06
  • CAS:616-02-4
  • Min. Order: 25KG
  • Purity: 98%min
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  • Citraconic anhydride
  • Citraconic anhydride pictures
  • $0.00 / 5kg
  • 2026-01-04
  • CAS:616-02-4
  • Min. Order: 1kg
  • Purity: 99.9%
  • Supply Ability: 500 tons
Citraconic anhydride Basic information
Product Name:Citraconic anhydride
Synonyms:alpha-methylmaleicanhydride;Anhydrid kyseliny citrakonove;anhydridkyselinycitrakonove;Citraconic acid anhydride;citraconicacidanhydride;Maleic anhydride, methyl-;methyl-maleicacidanhydride;methyl-maleicanhydrid
CAS:616-02-4
MF:C5H4O3
MW:112.08
EINECS:210-459-0
Product Categories:Anhydride Monomers;Monomers;Polymer Science;Carbonyl Compounds;Carboxylic Acid Anhydrides;Organic Building Blocks;Rubber & Plastic Auxiliary Agent
Mol File:616-02-4.mol
Citraconic anhydride Structure
Citraconic anhydride Chemical Properties
Melting point 6-10 °C (lit.)
Boiling point 213-214 °C (lit.)
density 1.247 g/mL at 25 °C (lit.)
vapor density 4 (vs air)
vapor pressure 1.3 hPa ( 47 °C)
refractive index n20/D 1.471(lit.)
Fp 215 °F
storage temp. Inert atmosphere,2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Liquid
color Clear colorless to very slightly yellow
Water Solubility decomposes
Sensitive Moisture Sensitive
BRN 1835
Dielectric constant40.3(20℃)
InChI1S/C5H4O3/c1-3-2-4(6)8-5(3)7/h2H,1H3
InChIKeyAYKYXWQEBUNJCN-UHFFFAOYSA-N
SMILESCC1=CC(=O)OC1=O
LogP-0.232 (est)
CAS DataBase Reference616-02-4(CAS DataBase Reference)
NIST Chemistry Reference2,5-Furandione, 3-methyl-(616-02-4)
EPA Substance Registry System2,5-Furandione, 3-methyl- (616-02-4)
Safety Information
Hazard Codes T
Risk Statements 23/24/25-36/37/38-42/43-34-24
Safety Statements 26-36/37/39-45-28A-23-36/37
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
RTECS GE6825000
10-21
TSCA TSCA listed
HazardClass 6.1
PackingGroup III
HS Code 29171990
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsEye Dam. 1
Resp. Sens. 1
Skin Corr. 1B
Skin Sens. 1
Hazardous Substances Data616-02-4(Hazardous Substances Data)
MSDS Information
ProviderLanguage
2-Methylmaleic anhydride English
SigmaAldrich English
ACROS English
ALFA English
Citraconic anhydride Usage And Synthesis
Chemical Propertiesclear colorless to very slightly yellow liquid
UsesReagent for alkalies, alcohols, and amines.
UsesCitraconic anhydride is used as a monomer for specialty unsaturated polyester resins. It is used to prepare bicyclic pyrrolidines, maleimides and co- and terpolymers. It is also used for the protection of N-terminal amino acids. Further, it is involved in the preparation of clothing ping acid and its amide. In addition to this, it is selectively used for the isolation of histidyl peptides.
UsesVersatile reagent used for the synthesis of maleimides, bicyclic pyrrolidines, and co- and terpolymers, as well as for the protection of N-terminal amino acids.
Flammability and ExplosibilityNon flammable
Reactions Citraconic anhydride is highly reactive due to the presence of anhydride groups and can undergo hydrolysis, esterification, amidation, and addition reactions.
Chemical Reactivity Citraconic anhydride (CA) is defined as a derivative of maleic anhydride that reacts with amines to form amide linkages at alkaline pH and can be hydrolyzed at acidic pH to release citraconic acid and free the amine, making it useful for temporarily blocking amine groups during molecular modifications.
Synthesis Citraconic anhydride was prepared by using alkaline earth metal oxides or alkaline earth metal sulfates as catalysts, and reacting for 1.0-10.0h at a mass ratio of itaconic acid and catalyst of 50:1 to 500:1, a mass ratio of itaconic acid and solvent of 1:1 to 1:10, and a reaction temperature of 130-210C, and recovering and reusing solvents;

Said alkaline earth metal oxide or alkaline earth metal sulfate catalyst is one of magnesium oxide, calcium oxide, barium oxide, strontium oxide, magnesium sulfate, calcium sulfate, barium sulfate, and strontium sulfate; and said solvent is one of xylene, o-dichlorobenzene, and tetrahydronaphthalene.

Purification MethodsPossible contamination is from the acid formed by hydrolysis. If the IR has OH bands, then reflux with Ac2O for 30minutes, evaporate, then distil the residue in a vacuum, otherwise distil in a vacuum. Store in a dry atmosphere. [Vaughan & Andersen J Am Chem Soc 77 6702 1955, Vaughan & Andersen J Org Chem 21 680 1956, Beilstein 17 H 440, 17 I 234, 17 II 448, 17 III/IV 5912, 17/11 V 65.]
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