Phenol red indicator - 0.1%(w/v)in water , CAS No.143-74-8

CAS: 143-74-8 Cat. No.: P196504 Molecular Weight: 354.38 EC Number: 205-609-7
AVAILABLE TO ORDER
GRADE & PURITY 0.1%(w/v)in water
Synonyms
3,3-bis(4-hydroxyphenyl)-3H-2,1lambda6-benzoxathiole-1,1-dione | 4,4'-(3H,2,1-Benzoxathiol-3-ylidene)bisphenol S,S-dioxide | Fenolipuna | Phenolsulfonephthalein | EINECS 205-609-7 | PHENOLSULFONPHTHALEIN [MART.] | PSP | Phenol, 4,4'-(1,1-dioxido-3H-2,1-be
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
500ml
P196504-500ml
3

$76.90

$89.90
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Why this grade

0.1%(w/v)in water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 35 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
3, 3-bis(4-hydroxyphenyl)-3H-2, 1lambda6-benzoxathiole-1, 1-dione | 4, 4'-(3H, 2, 1-Benzoxathiol-3-ylidene)bisphenol S, S-dioxide | Fenolipuna | Phenolsulfonephthalein | EINECS 205-609-7 | PHENOLSULFONPHTHALEIN [MART.] | PSP | Phenol, 4, 4'-(1, 1-dioxido-3H-2, 1-be
Specifications & Purity
0.1%(w/v)in water
Biochemical and Physiological Mechanisms
pH indicator widely used in culture media to identify pH changes from neutral (red) to acidic (yellow) values. Typically a change in color from red to yellow indicates high rates of cellular death when used in tissue cultures.
Storage
Room temperature
Shipped In
Normal
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Names and Identifiers
Canonical SmilesC1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC=C(C=C3)O)C4=CC=C(C=C4)O
IUPAC Name4-[3-(4-hydroxyphenyl)-1,1-dioxo-2,1λ6-benzoxathiol-3-yl]phenol
InChIKeyBELBBZDIHDAJOR-UHFFFAOYSA-N
INCHI1S/C19H14O5S/c20-15-9-5-13(6-10-15)19(14-7-11-16(21)12-8-14)17-3-1-2-4-18(17)25(22,23)24-19/h1-12,20-21H
Isomeric SMILES C1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC=C(C=C3)O)C4=CC=C(C=C4)O
Molecular Weight 354.38
Reaxy-Rn 326470
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=326470&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassBenzofurans
SubclassBenzofuranones
Intermediate Tree Nodes Not available
Direct ParentBenzofuranones
Alternative Parents Phthalides  Benzoxathioles  1-hydroxy-2-unsubstituted benzenoids  Organosulfonic acid esters  Benzene and substituted derivatives  Oxacyclic compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzofuranone - Phthalide - Benzoxathiole - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Oxacycle - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzofuranones. These are organic compounds containing a benzene ring fused to a furanone.
External Descriptors phenols - arenesulfonate ester - 2,1-benzoxathiole - sultone
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A498 (42825 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAKI-1 (44928 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KM12 (47707 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M14 (47487 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-3 (48710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-8 (47708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXF 393 (41971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-5 (47095 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SN12C (47755 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-19 (46794 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TK-10 (45540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-257 (46019 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-62 (47335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UO-31 (46270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI/ADR-RES (33767 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T47D (39041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EKVX (44102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCC 2998 (41480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-92 (41141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs-578T (29457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot NumberCertificate TypeDateItem
C2609333Certificate of AnalysisMar 17, 2026 P196504
Chemical and Physical Properties
Molecular Weight354.400 g/mol
XLogP33.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass354.056 Da
Monoisotopic Mass354.056 Da
Topological Polar Surface Area92.200 Ų
Heavy Atom Count25
Formal Charge0
Complexity545.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Hao Bai, Yuqing Liu, Linbo Gao, Tao Wang, Xiaoli Zhang, Jie Hu, Lisha Ding, Yueting Zhang, Qian Wang, Lei Wang, Jianlong Li, Zhifeng Zhang, Yang Wang, Chenlan Shen, Binwu Ying, Xiaoyu Niu, Wenchuang Hu.  (2023)  A portable all-in-one microfluidic device with real-time colorimetric LAMP for HPV16 and HPV18 DNA point-of-care testing.  BIOSENSORS & BIOELECTRONICS,      [PMID:38150799] [10.1016/j.bios.2023.115968]
2. Bo Yuan, Zicong Tan, Qiang Guo, Xiutong Shen, Chao Zhao, Jian Lin Chen, Yung-Kang Peng.  (2023)  Regulating the H2O2 Activation Pathway on a Well-Defined CeO2 Nanozyme Allows the Entire Steering of Its Specificity between Associated Enzymatic Reactions.  ACS Nano,      [PMID:37578491] [10.1021/acsnano.3c05409]
3. Ding Jianjun, Ye Li, Su Tong, Guo Naiyu, Yu Linbo, Miao Longxin, Cao Mian, Sun Chao.  (2023)  Three-dimensional open concave surface-enhanced Raman scattering sensor based on the SiO2/CNTs/AgNPs to detect the phenol red.  JOURNAL OF NANOPARTICLE RESEARCH,  25  (2): (1-14).  [PMID:] [10.1007/s11051-023-05684-8]
4. Yuechun Li, Han Zhang, Zhaowen Cui, Sijie Liu, Jingke Xu, Conghui Jia, Yaqian Chen, Lulu Wang, Jing Sun, Daohong Zhang, Mingqiang Zhu, Jianlong Wang.  (2022)  Chemical staining enhanced Enzyme-linked immunosorbent assay for sensitive determination of Clenbuterol in food.  FOOD CHEMISTRY,      [PMID:36055143] [10.1016/j.foodchem.2022.134012]
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8. Zeyang Liu, Hongyong Zhang, Zhen Zhan, Haochen Nan, Nan Huang, Tao Xu, Xiaohua Gong, Chengzhi Hu.  (2021)  Mild formation of core–shell hydrogel microcapsules for cell encapsulation.  Biofabrication,  13  (2): (025002).  [PMID:33271516] [10.1088/1758-5090/abd076]
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13. Wenyue Xie, Lingli Lei, Meiling Tian, Zeying Zhang, Yingshuai Liu.  (2018)  A high-resolution colorimetric immunoassay platform realized by coupling enzymatic multicolor generation with smartphone readout.  ANALYST,  143  (12): (2901-2907).  [PMID:29808208] [10.1039/C8AN00382C]
14. Jingjing Hu, Yanchun Quan, Yuping Lai, Zhao Zheng, Zhiqi Hu, Xinyu Wang, Tianjiao Dai, Qiang Zhang, Yiyun Cheng.  (2017)  A smart aminoglycoside hydrogel with tunable gel degradation, on-demand drug release, and high antibacterial activity.  JOURNAL OF CONTROLLED RELEASE,      [PMID:28077265] [10.1016/j.jconrel.2017.01.003]
15. Hui Zhi, Yingxi Qin, Yang Li, Fengya Wang, Liang Feng.  (2024)  A flexible, water anchoring, and colorimetric ionogel for sweat monitoring.  Biomaterials Science,      [PMID:39699242] [10.1039/D4BM01482K]
16. Yanshu Xiang, Yongjie Zhao, Yifan Jiang, Jiarui Feng, Xiaoyi Zhang, Wei Su, Yingjie Zhou, Peng Wei, Sze Shin Low, Hao Nan Li.  (2024)  Battery-Free and Multifunctional Microfluidic Janus Wound Dressing with Biofluid Management, Multi-Indicator Monitoring, and Antibacterial Properties.  ACS Applied Materials & Interfaces,      [PMID:39264683] [10.1021/acsami.4c09891]
17. Meng-Meng Du, Yuan-Cheng Wang, Bao-Chang Sun, Yong Luo, Liang-Liang Zhang, Guang-Wen Chu, Hai-Kui Zou.  (2025)  Biocatalytic kinetics of the reaction between CO2 and tertiary amine using carbonic anhydrase.  Chemical Engineering and Processing-Process Intensification,      [PMID:] [10.1016/j.cep.2025.110218]
18. Zhepeng Zhang, Yang Zhang, Chen Wang, Xianjin Liu, Hesham R. El-Seedi, Paula L. Gómez, Stella M. Alzamora, Xiaobo Zou, Zhiming Guo.  (2024)  Enhanced composite Co-MOF-derived sodium carboxymethyl cellulose visual films for real-time and in situ monitoring fresh-cut apple freshness.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2024.110475]
19. Rongli Li, Tongjun Yang, Mingtao Ding, Lihua Zhang, Haibo Xie.  (2025)  Gold nanoparticles supported on aldehyde-functionalized chitin nanocrystals as efficient catalysts in environmental catalysis.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39800037] [10.1016/j.ijbiomac.2025.139769]
20. Meng-Meng Du, Bao-Chang Sun, Bei-Bei Wang, Yong Luo, Liang-Liang Zhang, Guang-Wen Chu, Hai-Kui Zou, Jian-Feng Chen.  (2024)  Kinetic study on the reaction between CO2 and tertiary amine catalyzed by zinc(II) aza-macrocyclic complexes.  AICHE JOURNAL,  70  (4): (e18366).  [PMID:] [10.1002/aic.18366]
21. Xiaxia Yang, Linyan Yao, Xiuxia Sun, Lili Wang, Jianxi Xiao.  (2024)  Low-temperature DLP 3D printing of low-concentration collagen methacryloyl for the fabrication of durable and bioactive personalized scaffolds.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.155650]
22. Yanyu Yang, Ying Xiao, Xiang Wu, Junjie Deng, Rufang Wei, Ashuang Liu, Haiyang Chai, Rong Wang.  (2024)  Microgel-Crosslinked Thermo-Responsive Hydrogel Actuators with High Mechanical Properties and Rapid Response.  MACROMOLECULAR RAPID COMMUNICATIONS,      [PMID:38225681] [10.1002/marc.202300643]
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25. Wenqing Sun, Yufeng Xu, Zhiqin Liu, Wei Liu, Hongting Wang, Guanyu Chang, Zihui Yang, Zhen Dong, Jianguo Zeng.  (2024)  Studies on pharmacokinetic properties and intestinal absorption mechanism of sanguinarine chloride: in vivo and in situ.  TOXICOLOGY MECHANISMS AND METHODS,      [PMID:39087424] [10.1080/15376516.2024.2383366]
26. Zhibin Li, Guangtao Huang, Xiangqiang Dai, Mulan Qahar, Zi Ye, Minghui Wang, Jiawen Deng, Xiaoqi Zhang, Yan Zhou, Yu He, Shi Chen, Jun Wu.  (2025)  Laser-facilitated peroxidase-like hydrogel with simultaneous wound infection monitoring and eliminating.  BIOMATERIALS,      [PMID:40684643] [10.1016/j.biomaterials.2025.123542]
27. Zixin Zhu, Laiyi Liu, Qingyun Xie, Song Chen, Yiwan Sun, Chenjun Huang, Kyu-Jae Lee, Xue Gou, Xiaohong Li.  (2025)  Smart wound management with sustainable pH sensing and dynamic electrotherapy.  Acta Biomaterialia,      [PMID:40846093] [10.1016/j.actbio.2025.08.033]
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32. Qin Chen, Lei Wang, Siyu Li, Weifeng Zhao, Ka Li.  (2025)  A Multilayer Colorimetric Sponge Dressing with Unidirectional Exudate Drainage for Simultaneous Monitoring of pH and Moisture in Wound.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202520112]
33. Zixin Zhu, Qingyun Xie, Yiwan Sun, Fan Yan, Xiao Kang, Przemysław Zalewski, Xue Gou.  (2025)  Electrically controlled on-demand wound therapy based on real-time pH monitoring.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.162522]
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