Skip to Content
MilliporeSigma
All Photos(2)

Documents

319236

Sigma-Aldrich

Phenolphthalein solution

0.5 wt. % in ethanol: water (1:1)

Synonym(s):

C20H14O4; Phthalin;3,3-bis(4-hydroxyphenyl)-2-benzofuran-1-one

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C20H14O4
CAS Number:
Molecular Weight:
318.32
Beilstein/REAXYS Number:
284423
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

form

liquid

Quality Level

concentration

0.5 wt. % in ethanol: water (1:1)

color

colorless

visual transition interval

8.0-10, colorless to red

mp

-35 °C

density

0.918 g/mL at 25 °C

λmax

552 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Oc1ccc(cc1)C2(OC(=O)c3ccccc23)c4ccc(O)cc4

InChI

1S/C20H14O4/c21-15-9-5-13(6-10-15)20(14-7-11-16(22)12-8-14)18-4-2-1-3-17(18)19(23)24-20/h1-12,21-22H

InChI key

KJFMBFZCATUALV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Phenolphthalein is an acid base indicator. It is a weak acid, which is colorless in acidic solution and turns puce pink in alkaline solution. Phenolphthalein is genotoxic. It might cause oxidative damage and binds to estrogen receptors.
Phenolphthalein solution is a synthetic indicator. It is colorless in acidic and neutral conditions. Phenolphthalein gives pink color when added to a base, therefore it is considered as a base indicator.

Application

Phenolphthalein solution has been used to measure total titratable acids by titration method.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Charu Maini
Headstart Science (CCE), 7 (2017)
Cytokinin Treatment Modifies Litchi Fruit Pericarp Anatomy Leading to Reduced Susceptibility to Post-harvest Pericarp Browning
Fahima A, et al.
Plant Science (2019)
Phenolphthalein laxatives and risk of cancer
Coogan PF, et al.
Journal of the National Cancer Institute, 92(23), 1943-1944 (2000)
Physical Chemistry: Understanding our Chemical World (2008)
Amit Fahima et al.
Plant science : an international journal of experimental plant biology, 283, 41-50 (2019-05-28)
Litchi (Litchi chinensis Sonn.) is a subtropical fruit known for its attractive red pericarp color, semi-translucent white aril and unique flavor and aroma. Rapid post-harvest pericarp browning strictly limits litchi fruit marketing. In the current research, we hypothesized that modification

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service