Dimethylmaleinsureanhydrid

Dimethylmaleic anhydride

HCID 13010CAS 766-39-2

Grundinformationen

Standard-SMILES
CC1=C(C)C(=O)OC1=O
InChIKey
MFGALGYVFGDXIX-UHFFFAOYSA-N
Summenformel
C6H6O3
Durchschnittliche Molmasse
126,11 g/mol
Monoisotopische Masse
126,03169405

Überblick

2,3-Dimethylmaleic anhydride is a butenolide.

Namen und Bezeichner

Bevorzugter Name
Dimethylmaleic anhydride
IUPAC
3,4-dimethylfuran-2,5-dione
Lokaler Name
Dimethylmaleinsureanhydrid
Englischer Name
2,3-Dimethylmaleic anhydride
Summenformel
C6H6O3
Molmasse
126.11

Namen und Synonyme

2,3-DIMETHYLMALEIC ANHYDRIDE766-39-2Dimethylmaleic anhydride2,5-Furandione, 3,4-dimethyl-Pyrocinchonic anhydrideMaleic anhydride, dimethyl-Dimethylmaleic acid anhydridealpha,beta-Dimethylmaleic anhydride6PP3N541QADTXSID6061103NSC-92512RefChem:442539
Weitere Namen anzeigen
2,5-Furandione,3,4-dimethyl-2,2’-Dimethylmaleinsαureanhydrideic Anhydridepyrocinchonicanhydridedimethyl-maleicanhydrid3,4-dimethyl-5-furandioneTwoMethyl Maleic anhydride
2,3-dimethyl maleic anhydrideDTXCID5047902212-165-8DMMA3,4-dimethylfuran-2,5-dione3,4-Dimethyl-2,5-furandioneMFCD00005523HSDB 5517

Datenbank-Bezeichner

CAS
766-39-2
PubChem CID
13010
DTXSID
DTXSID6061103
ChEMBL
CHEMBL2270559
ChEBI
CHEBI:182178
UNII
6PP3N541QA
EC Number
212-165-8
Nikkaji
J36.810E

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,6
Polarare Oberfläche (TPSA)
43,4 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
0
Schwere Atome
9

Experimentelle und physikochemische Eigenschaften

PolymersPlastics & Rubber -> Acid Anhydrides, Cyclic
SpringerMaterials PropertiesChemical shift
Density1.107 AT 100 °C/4 °C
SolubilityVERY SOL IN ALCOHOL, ETHER, BENZENE, CHLOROFORM; SLIGHTLY SOL IN WATER
Boiling Point223 °C
Melting Point96 °C

Physikochemische Eigenschaften

Schmelzpunkt
93 · 93-96 °C (lit.)
Siedepunkt
223 °C · 223 °C (lit.)
Dichte
1.107 g/cm3 · 1.107 g/cm3 (100℃)
Brechungsindex
1.5627 · 1.5627 (estimate)
Flammpunkt
222 · 222-223°C
storage temp.
30 °C · Store below +30°C.

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

Warning

H302 (87.8%): 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 49 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Hazards SummaryMay decompose on exposure to moisture; May cause irritation; [MSDSonline] See ACID ANHYDRIDES.
Hazard Classes and CategoriesAcute Tox. 4 (87.8%)

Toxikologische Informationen

Interactions · 1 Eintrag

Modification with succinic anhydride of Clostridium perfringens epsilon prototoxin or toxin resulted in a loss of activation by trypsin or lethal activity, respectively. The prototoxin was more sensitive to succinylation than the toxin. On the other hand, the succinylated prototoxin was activated and cleaved by chymotrypsin, but not by trypsin. The lethal activity of the toxin was also lost after treatment with 2,3-dimethylmaleic anhydride or 2,4,6-trinitrobenzenesulfonic acid. When the 2,3-dimethylmaleic anhydride treated toxin treated with succinic anhydride or 2,4,6-trinitrobenzenesulfonic acid was incubated under acidic condition, it regained lethal activity. Thus modification of amino groups (lysine residues) prevented activation of the prototoxin by trypsin, and abolished lethal activity of the toxin.

Human Toxicity Excerpts · 1 Eintrag

THE MALEIC ANHYDRIDES, A SERIES OF REVERSIBLE ACYLATING AGENTS, PRODUCED THE ASPIRIN-TYPE DEFECT IN PLATELET AGGREGATION. UNLIKE THE ANTIPLATELET EFFECT OF ASPIRIN WHICH WAS IRREVERSIBLE, THE ANTIPLATELET EFFECT OF 2,3-DIMETHYLMALEIC ANHYDRIDE DISAPPEARED IN APPROXIMATELY 80 MINUTES AT 25 DEG.

Non-Human Toxicity Excerpts · 3 Einträge

2,3-DIMETHYLMALEIC ANHYDRIDE, A REAGENT REMOVING POSITIVE CELL SURFACE CHARGES, DECREASED THE AGGREGATION OF CHICK EMBRYO NEURAL RETINA CELLS IN CULTURE. TWENTY-FOUR HOURS AFTER 2,3-DIMETHYLMALEIC ANHYDRIDE WAS REMOVED FROM THE MEDIUM, THE MOBILITIES OF THE CELLS WERE SIMILAR TO THOSE OF THE CONTROLS.

ALPHA,BETA-DIMETHYLMALEIC ANHYDRIDE INDUCED SARCOMAS IN 3 OF 5 RATS. ARACHIS OIL, USED AS THE VEHICLE, WAS NONCARCINOGENIC IN 0.5 ML DOSES IN RATS.

THE REACTION OF DIMETHYLMALEIC ANHYDRIDE WITH AMINO GROUPS AT SURFACE OF THE EGGS OF SEA URCHIN DID NOT PREVENT FERTILIZATION.

Sicherheitsdaten

F
9-21
wgk
3
tsca
TSCA listed
hs_code
2917 19 80
RTECS-Nr.
ON4025000
risk_code
22

Chemie und Industrie

Verwendung und Herstellung

Uses · 2 Einträge

Used as a research chemical; No known commercial production in the US; [HSDB]

RESEARCH CHEM (CHEM INT FOR ORG SYNTH; PROTEIN REAGENT)

U.S. Production · 2 Einträge

(1979) NO EVIDENCE OF COMMERCIAL PRODN IN USA

(1981) NO EVIDENCE OF COMMERCIAL PRODN IN USA

Methods of ManufacturingDECARBOXYLATIVE DIMERIZATION OF MALEIC ANHYDRIDE IN THE PRESENCE OF 2-AMINOPYRIDINE
General Manufacturing Information2,5-Furandione, 3,4-dimethyl-: ACTIVE
Anwendungen · 1 Eintrag

Verwenden2,3-Dimethylmaleic anhydride can be usually used in the synthesis of maleimides and as an amino group protecting agent for superoxide dismutase. It is also used in the preparation of dimethylmaleic acid dimethyl ester. Further, it serves as a reactant in the dissociation of ribosomal proteins. In addition to this, The isolated molecule 2, 3-dimethylmaleic anhydride showed potent insecticidal activity in fumigation bioassay against several insect species, viz., adults of houseflies, cockroaches and stored-product insects.

Anbieter50 Anbieter

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Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: 2,3-Dimethylmaleic anhydride is a butenolide. It is a 5-membered cyclic anhydride with a double bond between carbon atoms C2 and C3. The double bond locks the molecule in a planar conformation and stabilizes the acid anhydride against hydration. It was used as linker to a cell penetrating peptidebased nanoparticle.

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