05-6560
m-Cresol Purple
JIS special grade
Synonym(s):
m-Cresolsulfonphthalein
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About This Item
Empirical Formula (Hill Notation):
C21H18O5S
CAS Number:
Molecular Weight:
382.43
EC Number:
218-960-6
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
350314
MDL number:
InChI key
OLQIKGSZDTXODA-UHFFFAOYSA-N
InChI
1S/C21H18O5S/c1-13-11-15(22)7-9-17(13)21(18-10-8-16(23)12-14(18)2)19-5-3-4-6-20(19)27(24,25)26-21/h3-12,22-23H,1-2H3
SMILES string
Cc1cc(O)ccc1\C(=C2/C=CC(=O)C=C2C)c3ccccc3S(O)(=O)=O
grade
JIS special grade
availability
available only in Japan
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Ali A Ensafi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(8-9), 2053-2057 (2004-07-14)
A new flow-injection method is reported for the determination of bromide. The method is based on catalytic effect of bromide on the oxidation of m-cresolsulfonephthalein by periodate in acidic media. The reaction was followed spectrophotometrically by measuring the decrease in
M D Johnston et al.
Journal of applied microbiology, 94(6), 1015-1023 (2003-05-20)
To examine the effect on the leakage of low molecular weight cytoplasmic constituents from Staphylococcus aureus using phenolics singly and in combination, and to see if the observations could be modelled using a non-linear dose response. The rate of potassium
A Noto et al.
Clinical chemistry, 29(10), 1713-1716 (1983-10-01)
We have developed a new spectrophotometric assay for urinary N-acetyl-beta-D-glucosaminidase (NAGase) with use of sodio m-cresolsulfonphthaleinyl N-acetyl-beta-D-glucosaminide (MCP-NAG). MCP-NAG was synthesized from acetochloro-glucosamine and m-cresolsulfonphthalein (MCP) in four steps. MCP-NAG reacts well with NAGase (Km = 0.41 mmol/L) and is
E Watanabe et al.
Biological & pharmaceutical bulletin, 23(7), 838-843 (2000-08-05)
Apparent membrane permeation coefficients (Papp) of poorly water-soluble drugs such as indomethacin (IDM) and triamterene (TAT) were obtained by the chamber method using an isolated rat intestinal tissue after solubilization of the drugs by additives. For the additives, sodium deoxycholate
J F Schindler et al.
Biochemistry, 38(18), 5772-5778 (1999-05-08)
The substrate specificities and product inhibition patterns of haloalkane dehalogenases from Xanthobacter autotrophicus GJ10 (XaDHL) and Rhodococcus rhodochrous (RrDHL) have been compared using a pH-indicator dye assay. In contrast to XaDHL, RrDHL is efficient toward secondary alkyl halides. Using steady-state
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