Basic information
- Standard SMILES
C=C1CC(=O)OC1=O- InChIKey
OFNISBHGPNMTMS-UHFFFAOYSA-N- Molecular formula
- C5H4O3
- Average molar mass
- 112.08 g/mol
- Monoisotopic mass
- 112.01604399
Names & identifiers
- Preferred name
- Itaconic Anhydride
- IUPAC
- 3-methylideneoxolane-2,5-dione
- English name
- Itaconic anhydride
- Molecular formula
- C5H4O3
- Molecular weight
- 112.08
Names & synonyms
Show more names
Database identifiers
- CAS
2170-03-8、25300-97-4- PubChem CID
- 75110
- DTXSID
DTXSID8062230- ChEMBL
CHEMBL87967- UNII
- Y455KS1U7Q
- EC Number
- 218-518-2
- Nikkaji
- J38.162D
Properties
Computed structural properties
- XLogP
- 0.2
- Topological polar surface area
- 43.4 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 0
- Heavy atoms
- 8
- Formal charge
- 0
- Complexity
- 169
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 66 · 66-68 °C (lit.)
- Boiling point
- 114 · 114-115 °C/12 mmHg (lit.)
- Density
- 1.26 · 1.2600
- refractive index
- 1.513 · 1.5130 (estimate)
- Flash point
- 114 · 114-115°C/12mm
- storage temp.
- 30 °C · Store below +30°C.
- form
- Crystalline Powder
- color
- White to cream
- Water Solubility
- Hydrolyzes in water.
- Sensitive
- Moisture Sensitive
- BRN
- 2212 · 2212
- InChI
- InChI=1S/C5H4O3/c1-3-2-4(6)8-5(3)7/h1-2H2
- InChIKey
- OFNISBHGPNMTMS-UHFFFAOYSA-N
- SMILES
- O1C(=O)CC(=C)C1=O
- CAS DataBase Reference
- 2170 · 2170-03-8(CAS DataBase Reference)
- FDA UNII
- 455 KS1U7Q · Y455KS1U7Q
- NIST Chemistry Reference
- 2 · 2,5-Furandione, dihydro-3-methylene-(2170-03-8)
- EPA Substance Registry System
- 2 · 2,5-Furandione, dihydro-3-methylene- (2170-03-8)
- UNSPSC Code
- 12162002 · 12162002
- NACRES
- 23 · NA.23
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H335
- Precautionary statements
- 261 · P261-P264-P271-P280-P302+P352-P305+P351+P338
- target organs
- Respiratory system
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36 · 36/37/38-22
- Safety Statements
- 26 · 26-36-24/25
- WGK Germany
- 3 · 3
- F
- 3 · 3-10-21
- TSCA
- TSCA listed
- HS Code
- 2917 · 2917 19 80
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 Skin · Eye Irrit. 2Skin Irrit. 2STOT SE 3
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
Warning
H302 (83.3%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 48 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Regulatory Information
Chemical: 2,5-Furandione, dihydro-3-methylene-
Status: Active Update: 03-02-2017 https://echa.europa.eu/registration-dossier/-/registered-dossier/18959
2,5-Furandione, dihydro-3-methylene-: Does not have an individual approval but may be used under an appropriate group standard
Safety data
- F
- 3-10-21
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 2917 19 80
- risk_code
- 36/37/38-22
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi,Xn
- safety_code
- 26-36-24/25
- Storage Class
- 11 - Combustible Solids
- target organs
- Respiratory system
- Hazard statements
- H315-H319-H335
- REACH Registrations
- Active
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P261-P264-P271-P280-P302+P352-P305+P351+P338
Chemistry & industry
Uses & manufacturing
Applications
UsesItaconic anhydride is used in immobilization of β-glucosidase. It undergoes estrification to obtain suitable monomers for emulsion polymerization itaconates.
General DescriptionItaconic anhydride (ITA) is a biobased material that is obtained from renewable resources. It is produced from the pyrolysis of citric acid or by fermenting carbohydrates which forms itanoic acid. Itanoic acid can be dehydrated to form an anhydride. It is relatively more reactive that maleic anhydride and can be used as an alternating monomer that facilitates the introduction of polar functionalities in polymers.
Preparation methods
PreparationTo a flask equipped with a 12 mm diameter ground glass adaptor tube bent for downward distillation and joined to a 100 cm condenser is added 200 gm (0.95 mole) of citric acid monohydrate. An ice-cooled flask and a cold trap are connected to the condenser. The flask containing the citric acid is heated rapidly with a wide flame of the Meker burner so that in 12-15 min the distillation at 175-190°C is complete. The distillation is stopped earlier if the vapors in the reaction flask become yellow. Superheating of the citric acid will cause rearrangement to citraconic anhydride. The water is quickly separated from the distillate and the itaconic anhydride layer dried to afford 40-50 gm (37-47%), m.p. 67-68°C. Long time contact of the water with the anhydride causes it to hydrolyze to itaconic acid, m.p. 162-165°C.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Related reactions
Linked notes
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