M89803
Mucochloric acid
99%
Synonym(s):
2,3-Dichloromalealdehydic acid
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About This Item
Linear Formula:
OHCCCl=CClCOOH
CAS Number:
Molecular Weight:
168.96
Beilstein:
1705641
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
crystals
mp
125-128 °C (lit.)
SMILES string
OC(=O)\C(Cl)=C(/Cl)C=O
InChI
1S/C4H2Cl2O3/c5-2(1-7)3(6)4(8)9/h1H,(H,8,9)/b3-2+
InChI key
LUMLZKVIXLWTCI-NSCUHMNNSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
Flash Point(F)
366.8 °F
Flash Point(C)
186 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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L Kronberg et al.
Chemical research in toxicology, 5(6), 852-855 (1992-11-01)
Mucochloric acid, a genotoxic hydroxyfuranone found in chlorinated drinking water, was reacted with cytidine, adenosine, guanosine, and uridine. HPLC analyses with UV detection at 290 nm showed that one major product peak was formed in the reactions of cytidine, adenosine
Oxidation and radical intermediates associated with the glutathione conjugation of mucochloric acid.
R T LaLonde et al.
Chemical research in toxicology, 7(4), 482-486 (1994-07-01)
The inactivation of the drinking water mutagen mucochloric acid (MCA) by reduced glutathione (GSH) was linked to the formation of an MCA-GSH conjugate, a nonmutagen in the Salmonella typhimurium (TA100) plate incorporation assay. Anaerobic formation of MCA-GSH is found now
D Asplund et al.
Chemical research in toxicology, 8(6), 841-846 (1995-09-01)
The bacterial mutagen mucochloric acid was reacted with adenosine in aqueous solutions at 37 degrees C. In the HPLC chromatograms of the reaction mixtures two peaks of unidentified products were observed at longer retention times than the previously characterized "etheno"
Ji Zhang et al.
Organic letters, 5(4), 553-556 (2003-02-14)
[reaction: see text] The first direct reductive amination of mucochloric acid (1) has been accomplished. Reaction of 1 with various alkyl, aryl, and benzylamines, followed by reduction in the same pot, provides an efficient method of obtaining N-benzyl-3,4-dichloro-1,5-dihydro-pyrrol-2-one and N-aryl
R T LaLonde et al.
Chemical research in toxicology, 5(5), 618-624 (1992-09-01)
The Salmonella typhimurium (TA100) mutagenic compound, mucochloric acid [3,4-dichloro-5-hydroxy-2(5H)-furanone (MCA)], was inactivated by in vitro N-acetylcysteine (NAC). The reaction of MCA with NAC at pH7 was second order and gave products 4, 5, and 6a that resulted from the displacement
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