Coumarin 7 (Highly Pure)


Catalog Number: B2012330 (50 mg)
Coumarin 7 (Highly Pure) is a high quality laser dye. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Coumarin 7 (Highly Pure)
Catalog number: B2012330
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 50 mg
Molecular Weight or Concentration: 333.4 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: 3-(1H-benzimidazol-2-yl)-7-(diethylamino)-2H-1-benzopyran-2-one
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Lu Y, Cederbaum AI. Cytochrome P450s and Alcoholic Liver Disease Curr Pharm Des. 2018;24(14):1502-1517.
2: Pelkonen O, Rautio A, Raunio H, Pasanen M. CYP2A6: a human coumarin 7-hydroxylase Toxicology. 2000 Apr 3;144(1-3):139-47.
3: Das A, Das S, Biswas A, Chattopadhyay N. Exploration of Self-Aggregation of Coumarin_7 and Coumarin 30 in Water: Role of β-Cyclodextrin as a Modulator J Phys Chem B. 2021 Dec 16;125(49):13482-13493.
4: Cheriyan BV Sr, Kadhirvelu P Sr, Nadipelly J Jr, Shanmugasundaram J, Sayeli V Sr, Subramanian V Sr. Anti-nociceptive Effect of 7-methoxy Coumarin from Eupatorium Triplinerve vahl (Asteraceae) Pharmacogn Mag. 2017 Jan-Mar;13(49):81-84.
5: Zhang SG, Wan YQ, Wen Y, Zhang WH. Novel Coumarin_7-Carboxamide/Sulfonamide Derivatives as Potential Fungicidal Agents: Design, Synthesis, and Biological Evaluation Molecules. 2022 Oct 14;27(20):6904.
6: Pelkonen O, Rautio A, Raunio H, Mäenpää J, Hakkola J. Regulation of coumarin_7-hydroxylation in man J Cancer Res Clin Oncol. 1994;120 Suppl:S30-1.
7: Rauma AL, Rautio A, Pasanen M, Pelkonen O, Törrönen R, Mykkänen H. Coumarin_7-hydroxylation in long-term adherents of a strict uncooked vegan diet Eur J Clin Pharmacol. 1996;50(1-2):133-7.
8: Srivastava S, Maikhuri VK, Kumar R, Bohra K, Singla H, Maity J, Prasad AK. Synthesis and Photophysical Studies on N(1)-(2′-O,4′-C-Methyleneribofurano-nucleoside-3′-yl)-C(4)-(coumarin_7-oxymethyl)-1,2,3-triazoles Carbohydr Res. 2018 Dec;470:19-25.
9: Ritschel WA, Brady ME, Tan HS, Hoffmann KA, Yiu IM, Grummich KW. Pharmacokinetics of coumarin and its 7-hydroxy-metabolites upon intravenous and peroral administration of coumarin in man Eur J Clin Pharmacol. 1977 Dec 28;12(6):457-61.
10: Min BK, Hyun DG, Jeong SY, Kim YH, Ma ES, Woo MH. A new cytotoxic coumarin, 7-[(E)-3′,7′-dimethyl-6′-oxo-2′,7′-octadienyl] oxy coumarin, from the leaves of Zanthoxylum schinifolium Arch Pharm Res. 2011 May;34(5):723-6.

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