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Merck
CN

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:
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grade

JIS special grade

availability

available only in Japan

SMILES string

Cc1cc(O)ccc1\C(=C2/C=CC(=O)C=C2C)c3ccccc3S(O)(=O)=O

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

InChI key

OLQIKGSZDTXODA-UHFFFAOYSA-N



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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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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
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