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Key Documents

M89803

Sigma-Aldrich

Mucochloric acid

99%

Sinonimo/i:

2,3-Dichloromalealdehydic acid

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About This Item

Formula condensata:
OHCCCl=CClCOOH
Numero CAS:
Peso molecolare:
168.96
Beilstein:
1705641
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

99%

Forma fisica

crystals

Punto di fusione

125-128 °C (lit.)

Stringa SMILE

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+
LUMLZKVIXLWTCI-NSCUHMNNSA-N

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Categorie correlate

Pittogrammi

Skull and crossbonesCorrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

366.8 °F

Punto d’infiammabilità (°C)

186 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges


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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
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"
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
I L Steffensen et al.
Pharmacology & toxicology, 85(2), 56-64 (1999-09-17)
Epidemiological studies indicate an association between exposure to chlorinated drinking water and risk of intestinal cancer. In order to study this experimentally, we have examined the effects of 3,4-dichloro-5-hydroxy-2[5H]-furanone (mucochloric acid, MCA) and 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX), mutagenic and genotoxic compounds in
B Isomaa et al.
Toxicology, 100(1-3), 69-77 (1995-06-26)
The cytotoxicity of the, in Salmonella, potent mutagenic compound, 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) and its structural analogue 3,4-dichloro-5-hydroxy-2[5H]-furanone (mucochloric acid, MCA), was studied in freshly isolated rainbow trout hepatocytes and gill epithelial cells by determining 86Rb-leakage and decrease in fluorescence intensity in

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