Cresol red
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Cresol red
structure -
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CAS No:
1733-12-6
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Formula:
C21H18O5S
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Chemical Name:
Cresol red
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Synonyms:
Phenol,4,4′-(1,1-dioxido-3H-2,1-benzoxathiol-3-ylidene)bis[2-methyl-;o-Cresol,4,4′-(3H-2,1-benzoxathiol-3-ylidene)di-,S,S-dioxide;o-Cresolsulfonephthalein;Phenol,4,4′-(3H-2,1-benzoxathiol-3-ylidene)bis[2-methyl-,S,S-dioxide;o-Toluenesulfonic acid,α-hydroxy-α,α-bis(4-hydroxy-m-tolyl)-,γ-sultone;3H-2,1-Benzoxathiole,phenol deriv.;4,4′-(1,1-Dioxido-3H-2,1-benzoxathiol-3-ylidene)bis[2-methylphenol];o-Cresol Red;o-Cresolsulfonphthalein;Cresol red;3′,3′′-Dimethylphenolsulfonephthalein;Cresolsulfophthalein;NSC 7224;32210-84-7
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CAS No:
Description
Dark green or brown-red powderChEBI: A member of the class of 2,1-benzoxathioles that is 2,1-benzoxathiole 1,1-dioxide in which both of the hydrogens at position 3 have been substituted by 4-hydroxy-5-methylphenyl groups.
Cresol red is a member of the class of 2,1-benzoxathioles that is 2,1-benzoxathiole 1,1-dioxide in which both of the hydrogens at position 3 have been substituted by 4-hydroxy-5-methylphenyl groups. It has a role as an acid-base indicator, a dye and a two-colour indicator. It is a 2,1-benzoxathiole, an arenesulfonate ester, a polyphenol and a sultone.
Characteristics
92.2
3.94
Dark green or brown-red Powder
0.98 g/mL at 25 °C
>300 °C
479.59°C (rough estimate)
293.6±30.1 °C
1.5300 (estimate)
Solubility Sparingly soluble in water; soluble in ethanol
Store at RT.
Safety Information
UN1170 - class 3 - PG 3 - Ethanol, solution
3
36/37/38-20/21/22-11
24/25-36-26-16
Xi,Xn,F
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
|Warning|H315 (97.67%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Cresol red Use and Manufacturing
Toluenesulfonic anhydride, o-cresol, and anhydrous zinc chloride are mixed, stirred and heated, and the condensation reaction is carried out at 115-120°C for about 7 hours, and the remaining o-cresol is purged by steam. Filter, the filter cake is dissolved with hot sodium carbonate aqueous solution, filter, add 1:1 hydrochloric acid to the clear filtrate to neutralize, and stir vigorously. The crystals were filtered out, washed with a small amount of water, and dried to obtain the finished product. If necessary, it can be purified by recrystallization from glacial acetic acid.
Acid-base indicator.
Phenol, 4,4'-(1,1-dioxido-3H-2,1-benzoxathiol-3-ylidene)bis[2-methyl-: ACTIVE
Computed Properties
Molecular Weight:382.4
XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:382.08749484
Monoisotopic Mass:382.08749484
Topological Polar Surface Area:92.2
Heavy Atom Count:27
Complexity:615
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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