Date published: 2025-9-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

7-Hydroxy-4-(trifluoromethyl)coumarin (CAS 575-03-1)

0.0(0)
Write a reviewAsk a question

See product citations (2)

Alternate Names:
4-(Trifluoromethyl)umbelliferone
Application:
7-Hydroxy-4-(trifluoromethyl)coumarin is a fluorescent pH-indicator
CAS Number:
575-03-1
Purity:
≥97%
Molecular Weight:
230.14
Molecular Formula:
C10H5F3O3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

7-Hydroxy-4-(trifluoromethyl)coumarin is useful as a fluorescent pH-indicator. 7-Hydroxy-4-(trifluoromethyl)coumarin, also referred to as 7-hydroxy-4-trifluoromethylcoumarin or 7-hydroxy-4-TFMC, is a highly fluorescent compound extensively employed in scientific research. As a member of the coumarin family of compounds, it features a distinctive benzopyran-2-one ring structure. The exceptional fluorescence of 7-Hydroxy-4-TFMC becomes apparent with an excitation peak at 360 nm and an emission peak at 460 nm. This unique property makes it an ideal choice as a fluorescent dye for imaging purposes and as a fluorescent probe to detect various biological molecules. The significance of 7-Hydroxy-4-TFMC in scientific research lies in its ability to efficiently interact with a diverse array of biological molecules. This compound serves as an indispensable tool for detecting and quantifying the concentration of vital biomolecules like proteins, nucleic acids, and small molecules. Furthermore, it enables researchers to visualize critical biological processes, such as cell cycle progression and protein-protein interactions. The versatility of 7-Hydroxy-4-TFMC extends to its application as a fluorescent dye, facilitating the labeling and tracking of cells, proteins, and other molecules in live cells and tissues. The binding mechanisms of 7-Hydroxy-4-TFMC with various biological molecules are equally noteworthy. Its interactions with proteins involve electrostatic attractions, hydrogen bonding, and hydrophobic interactions. When it comes to nucleic acids, hydrogen bonding and electrostatic interactions play a key role in the binding process. Additionally, this compound can effectively bind to small molecules through hydrogen bonding and hydrophobic interactions, further broadening its utility in scientific investigations.


7-Hydroxy-4-(trifluoromethyl)coumarin (CAS 575-03-1) References

  1. Isolation and characterization of a UDP-glucuronosyltransferase (UGT1A01) cloned from female rhesus monkey.  |  Dean, B., et al. 2002. Arch Biochem Biophys. 402: 289-95. PMID: 12051676
  2. Identification of UGT2B9*2 and UGT2B33 isolated from female rhesus monkey liver.  |  Dean, B., et al. 2004. Arch Biochem Biophys. 426: 55-62. PMID: 15130782
  3. Quaternary ammonium-linked glucuronidation of tamoxifen by human liver microsomes and UDP-glucuronosyltransferase 1A4.  |  Kaku, T., et al. 2004. Biochem Pharmacol. 67: 2093-102. PMID: 15135306
  4. Quantitative analysis of antiretroviral drugs in lysates of peripheral blood mononuclear cells using MALDI-triple quadrupole mass spectrometry.  |  van Kampen, JJ., et al. 2008. Anal Chem. 80: 4969-75. PMID: 18533679
  5. Amino acid positions 69-132 of UGT1A9 are involved in the C-glucuronidation of phenylbutazone.  |  Nishiyama, T., et al. 2008. Arch Biochem Biophys. 478: 75-80. PMID: 18602884
  6. Chemoenzymatic synthesis of two new halogenated coumarin glycosides as potential antifungal agents.  |  Zhou, L., et al. 2012. Nat Prod Commun. 7: 1331-2. PMID: 23157002
  7. Base-induced phototautomerization in 7-hydroxy-4-(trifluoromethyl)coumarin.  |  Westlake, BC., et al. 2012. J Phys Chem B. 116: 14886-91. PMID: 23190375
  8. High-throughput fluorescence assay of cytochrome P450 3A4.  |  Cheng, Q. and Guengerich, FP. 2013. Methods Mol Biol. 987: 157-62. PMID: 23475676
  9. Intermolecular proton shuttling in excited state proton transfer reactions: insights from theory.  |  Savarese, M., et al. 2014. Phys Chem Chem Phys. 16: 8661-6. PMID: 24676232
  10. Intrinsic and dynamical reaction pathways of an excited state proton transfer.  |  Raucci, U., et al. 2015. J Phys Chem B. 119: 2650-7. PMID: 25517266

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Hydroxy-4-(trifluoromethyl)coumarin, 250 mg

sc-210622
250 mg
$32.00

7-Hydroxy-4-(trifluoromethyl)coumarin, 1 g

sc-210622A
1 g
$66.00