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Merck
CN

M89803

Mucochloric acid

99%

Synonym(s):

2,3-Dichloromalealdehydic acid

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About This Item

Linear Formula:
OHCCCl=CClCOOH
CAS Number:
87-56-9
Molecular Weight:
168.96
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897301
EC Number:
201-752-4
Beilstein/REAXYS Number:
1705641
MDL number:
MFCD00006966
Assay:
99%
Form:
crystals

Key Documents

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InChI

1S/C4H2Cl2O3/c5-2(1-7)3(6)4(8)9/h1H,(H,8,9)/b3-2+

InChI key

LUMLZKVIXLWTCI-NSCUHMNNSA-N

SMILES string

OC(=O)\C(Cl)=C(/Cl)C=O

assay

99%

form

crystals

mp

125-128 °C (lit.)

Quality Level

100

Related Categories

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

wgk

WGK 2

flash_point_f

366.8 °F

flash_point_c

186 °C

ppe

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

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
STBL1457
STBK9418
STBK0865
STBJ3843
STBG7204

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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
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
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
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