C82604
Citraconic acid
98%
Synonym(s):
Methylmaleic acid
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About This Item
Linear Formula:
CH3C(CO2H)=CHCO2H
CAS Number:
Molecular Weight:
130.10
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-858-7
Beilstein/REAXYS Number:
1722679
Assay:
98%
Form:
crystals
InChI
1S/C5H6O4/c1-3(5(8)9)2-4(6)7/h2H,1H3,(H,6,7)(H,8,9)/b3-2-
InChI key
HNEGQIOMVPPMNR-IHWYPQMZSA-N
SMILES string
C\C(=C\C(O)=O)C(O)=O
assay
98%
form
crystals
mp
88-94 °C (lit.)
Quality Level
Related Categories
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
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Nikolai P Bityutskii et al.
Journal of plant physiology, 218, 100-108 (2017-08-19)
Aluminium (Al) is one of the major stressors for plants in acidic soils, negatively affecting plant growth and nutrient balances. Significant efforts have been undertaken to understand mechanisms of Al tolerance in plants. However, little is known of the relevance
K S Rao et al.
Journal of ethnopharmacology, 60(3), 207-213 (1998-06-05)
Monomethyl fumarate, isolated for the first time from the methanolic extract of the whole plant of Fumaria indica, was characterised and screened for its antihepatotoxic activity in albino rats. The compound showed significant (P < 0.01) antihepatotoxic activity against thioacetamide
Katrin Wallbrecht et al.
Experimental dermatology, 20(12), 980-985 (2011-10-15)
Although fumaric acid esters (FAE) have a decade-long firm place in the therapeutic armamentarium for psoriasis, their pleiotropic mode of action is not yet fully understood. While most previous studies have focused on the effects of FAE on leucocytes, we
Edward Guccione et al.
Environmental microbiology, 12(3), 576-591 (2009-11-19)
Methylmenaquinol : fumarate reductase (Mfr) is a newly recognized type of fumarate reductase present in some epsilon-proteobacteria, where the active site subunit (MfrA) is localized in the periplasm, but for which a physiological role has not been identified. We show
Yuichiro Himeda et al.
Dalton transactions (Cambridge, England : 2003), (32)(32), 6286-6288 (2009-08-06)
Deuterium-labelled compounds were prepared by (transfer) deuterogenation of unsaturated compounds using H(2) or HCO(2)H in acidic D(2)O as deuterium source with almost quantitative yields and high deuterium contents under mild reaction conditions via heterolytic cleavage of H(2) (or decomposition of
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