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63200

Sigma-Aldrich

Maleic anhydride

puriss., ≥99.0% (NT)

Synonym(s):

2,5-Furandione

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About This Item

Empirical Formula (Hill Notation):
C4H2O3
CAS Number:
Molecular Weight:
98.06
Beilstein:
106909
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

3.4 (vs air)

Quality Level

vapor pressure

0.16 mmHg ( 20 °C)

grade

puriss.

Assay

≥99.0% (NT)

form

flakes
powder or crystals

autoignition temp.

870 °F

expl. lim.

7.1 %

bp

200 °C (lit.)

mp

51-56 °C (lit.)
52-54 °C

SMILES string

O=C1OC(=O)C=C1

InChI

1S/C4H2O3/c5-3-1-2-4(6)7-3/h1-2H

InChI key

FPYJFEHAWHCUMM-UHFFFAOYSA-N

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General description

Maleic anhydride is a dehydration product of maleic acid that is of considerable industrial importance.

Application

Maleic anhydride has been used as a reference standard for the determination of the analyte in:
  • Workplace air samples by capillary gas chromatography combined with electron capture detection (GC-ECD).

It may be used as a derivatization agent for fatty alcohol ethoxylates in:
  • Industrial mixtures, cleaning products and river and sea waters by high performance liquid chromatography (HPLC) coupled with ultraviolet-visible (UV-Vis) diode array detection (DAD).

Other Notes

For the complete dissociation of enzymes into soluble subunits; For the reversible blocking of amino groups (lysine reagent); P.J.G. Butler, J.I. Harris, B.S. Hartley, R. Lebermann; For the maleylation of proteins

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1A - STOT RE 1 Inhalation

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 1

Flash Point(F)

217.4 °F - closed cup

Flash Point(C)

103 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The Biochemical Journal, 103, 78-78 (1967)
Dissociation of protein subunits by maleylation.
C L Sia et al.
Biochemical and biophysical research communications, 31(5), 731-737 (1968-06-10)
Areti Tzereme et al.
Polymers, 11(3) (2019-04-10)
The main purpose of this study was to investigate the synthesis of some cross-linked carboxyl-grafted chitosan derivatives to be used as selective adsorbents for diclofenac (DCF) pharmaceutical compounds from aqueous mixtures. Four different materials were synthesized using succinic anhydride (CsSUC)
Determination of maleic anhydride in occupational atmospheres.
Pfaffli P, et al.
Journal of Chromatography A, 982(2), 261-266 (2002)
[46] Acylation with dicarboxylic acid anhydrides.
M H Klapper et al.
Methods in enzymology, 25, 531-536 (1972-01-01)

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