D167800
2,3-Dimethylmaleic anhydride
98%
Synonym(s):
Dimethylmaleic anhydride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C6H6O3
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
212-165-8
Beilstein/REAXYS Number:
112044
MDL number:
Product Name
2,3-Dimethylmaleic anhydride, 98%
InChI key
MFGALGYVFGDXIX-UHFFFAOYSA-N
InChI
1S/C6H6O3/c1-3-4(2)6(8)9-5(3)7/h1-2H3
SMILES string
CC1=C(C)C(=O)OC1=O
assay
98%
form
flakes
bp
223 °C (lit.)
mp
93-96 °C (lit.)
Application
Reagent used in the synthesis of maleimides and as an amino group protecting agent for superoxide dismutase.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Kabrambam D Singh et al.
Scientific reports, 7(1), 12483-12483 (2017-10-04)
Evolution of resistance among insects to action of pesticides has led to the discovery of several insecticides (neonicotinoids and organophosphates) with new targets in insect nervous system. Present study evaluates the mode of inhibition of acetylchlonesterase (AChE), biochemical efficacy, and
S Tsunoda et al.
The Journal of pharmacology and experimental therapeutics, 290(1), 368-372 (1999-06-25)
We attempted to develop a novel method for the chemical modification of cytokines with synthetic polymers to increase in vivo therapeutic efficacy. A pH-reversible amino-protective reagent, dimethylmaleic anhydride (DMMAn), was used for polymer conjugation of tumor necrosis factor-alpha (TNF-alpha) with
Se Rim Yoon et al.
Journal of biomedical materials research. Part A, 100(8), 2027-2033 (2012-05-15)
A charge-converting and pH-dependent nanocarrier was achieved by conjugating 2,3-dimethylmaleic anhydride (DMMA) to the amino group of an octadecyl grafted poly (2-hydroxyethyl aspartamide) (PHEA-g-C(18)-NH(2)) backbone, thereby forming a spherical micelle. PHEA, a poly(amino acid)s derivative, was derived from poly(succinimide), which
C Vard et al.
The Journal of biological chemistry, 272(32), 20259-20262 (1997-08-08)
The acidic ribosomal proteins P1-P2 from rat liver were overproduced for the first time by expression of their cDNA in Escherichia coli. They were tested for their ability to reactivate inactive P1-P2-deficient core particles derived from 60 S ribosomal subunits
J. Controlled Release, 28, 203-203 (1994)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service