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M89803

Sigma-Aldrich

Mucochloric acid

99%

Sinónimos:

2,3-Dichloromalealdehydic acid

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About This Item

Fórmula lineal:
OHCCCl=CClCOOH
Número de CAS:
87-56-9
Peso molecular:
168.96
Beilstein/REAXYS Number:
1705641
EC Number:
201-752-4
MDL number:
MFCD00006966
UNSPSC Code:
12352100
PubChem Substance ID:
24897301
NACRES:
NA.22

Quality Level

100

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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Categorías relacionadas

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

Storage Class

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

wgk_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
STBL1457
STBK9418
STBK0865
STBJ3843
STBG7204

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R T LaLonde et al.
Environmental and molecular mutagenesis, 22(3), 181-187 (1993-01-01)
A difference in biological response to enantiomers is not an uncommon observation and is, therefore, to be expected in various manifestations of genotoxicity. The bacterial mutagen mucochloric acid (2,3-dichloro-5-hydroxy-2(5H)-furanone) has one chiral center, at C-5, but this mutagen exists in
I R Politzer et al.
Archives of environmental contamination and toxicology, 20(3), 371-374 (1991-04-01)
Cyclodextrins form inclusion complexes with a wide range of guest molecules which wholly, or in part, fit into their hydrophobic cavity. Since no covalent bonds are formed in this complexation, the guests can subsequently be eluted. The possibility of such
Koushik Das Sarma et al.
The Journal of organic chemistry, 72(9), 3311-3318 (2007-04-03)
Novel 5-(1'-hydroxy)-gamma-butyrolactone and gamma-butyrolactam subunits were synthesized by direct vinylogous aldol addition of alpha,beta-dichloro gamma-butyrolactones and gamma-butyrolactams with aldehydes under basic conditions. Different bases and solvents were screened in the context of generating gamma-butyrolactones. Diastereoselectivity was observed and gamma-butenolides and
L Kronberg et al.
Chemical research in toxicology, 9(8), 1257-1263 (1996-12-01)
Mucochloric (MCA) and mucobromic acid (MBA)--bacterial mutagens and water disinfection byproducts--were reacted with adenosine, cytidine, and guanosine in N,N-dimethylformamide (DMF). In the MCA reaction with adenosine and cytidine and in the MBA reaction with adenosine one major product was formed.
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
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