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Definition of Dihydrocoumarin CAS 119-84-6
Dihydrocoumarin CAS 119-84-6 is a common compound found in sweet clover that has been studied as a disruptor of epigenetic processes in cells. Epigenetic processes control gene expression within a cell and are highly influenced by environmental factors. Epigenomic disruptions change which genes are expressed and to what extent and are not linked to DNA mutations. Dihydrocoumarin has been shown to inhibit the sirtuin deacetylase family, specifically Sir2, SIRT1, and SIRT2.
3-Phenylpropionic Acid / Hydrocinnamic Acid CAS 501-52-0
Product name:3-Phenylpropionic acid
CAS:501-52-0
MF:C9H10O2
MW:150.17
Melting point:45-48°C
Packaging:1 kg/bottle, 25 kg/drum, 200 kg/drum
Methyl 3-Phenylpropanoate / 3-Phenylpropionic Acid Methyl Ester CAS 103-25-3
Product name:3-Phenylpropionic acid methyl ester
CAS:103-25-3
MF:C10H12O2
MW:164.2
Density:1.043 g/ml
Boiling point:239°C
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
P-Tolualdehyde / 4-Methylbenzaldehyde CAS 104-87-0
Product name:4-Methylbenzaldehyde
CAS:104-87-0
MF:C8H8O
MW:120.15
Density:1.12 g/ml
Melting point:-6°C
Boiling point:248°C
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
Phenethyl Cinnamate CAS 103-53-7
Product name:Phenethyl cinnamate
CAS:103-53-7
MF:C17H16O2
MW:252.31
Melting point:54-58°C
Flash point:113°C
Density:1.045-1.048 g/cm3
Packaging:1 kg/bag, 25 kg/drum
Product name:Benzyl cinnamate
CAS:103-41-3
MF:C16H14O2
MW:238.28
Density:1.11 g/cm3
Melting point:35-36°C
Packaging:200 kg/drum
P-Anisaldehyde / 4-Methoxybenzaldehyde CAS 123-11-5
Product name:4-Methoxybenzaldehyde
CAS:123-11-5
MF:C8H8O2
MW:136.15
Melting point:-1°C
Boiling point:248°C
Density:1.121 g/ml
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
Allyl Cyclohexylpropionate CAS 2705-87-5
Product name:Allyl cyclohexylpropionate
CAS:2705-87-5
MF:C12H20O2
MW:196.29
Boiling point:91°C
Density:0.948 g/ml
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
Product name:Styralyl acetate
CAS:93-92-5
MF:C10H12O2
MW:164.2
Density:1.028 g/ml
Melting point:-60°C
Boiling point:94-95°C
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
Product name:Oleamide
CAS:301-02-0
MF:C18H35NO
MW:281.48
Packaging:1 L/bottle, 25 L/drum, 200 L/drum
Benefits of Using Dihydrocoumarin CAS 119-84-6
Dihydrocoumarin CAS 119-84-6 is used in medicine as a drug for treating oedemas. Isolated coumarin must not be added to foods. If it is contained in parts of plants added to foods to flavour them (as is the case with cinnamon), the coumarin quantity is, according to the new European aroma law, restricted for certain cinnamon-containing foods.
What Does Dihydrocoumarin CAS 119-84-6 Do to Blood?
Coumarin was first discovered in Tonka bean and then widely in other plants. Coumarin has an anticoagulant effect, and its derivative, warfarin, is a vitamin K analogue that inhibits the synthesis of clotting factors and is more widely used in the clinical treatment of endovascular embolism.
At present, many artificial chemical synthesis methods can be used to modify the structure of coumarin to develop many effective drugs with low toxicity. In this study, we investigated the effects of six coumarin derivatives on the platelet aggregation induced by adenosine diphosphate (ADP). We found that the six coumarin derivatives inhibited the active form of GPIIb/IIIa on platelets and hence inhibit platelet aggregation. We found that 7-hydroxy-3-phenyl 4H-chromen-4-one (7-hydroxyflavone) had the most severe effect.
We further analyzed the downstream signal transduction of the ADP receptor, including the release of calcium ions and the regulation of cAMP, which were inhibited by the six coumarin derivatives selected in this study. These results suggest that coumarin derivatives inhibit coagulation by inhibiting the synthesis of coagulation factors and they may also inhibit platelet aggregation.

What Is the Function of Dihydrocoumarin CAS 119-84-6 in Plants?
Coumarin is an unsaturated lactone that serves as a secondary metabolite and is commonly found in monocotyledonous and dicotyledonous plants, with a particular prevalence in Umbelliferae, Rutaceae, Leguminosae, Orchidaceae and Gramineae. Coumarins are mainly produced in the leaves, fruits and roots of plants. The coumarin is a powerful inhibitor against seed germination and it can also inhibit the growth of lateral roots and plant development. Additionally, coumarin exhibits various effects on antioxidant, antibacterial, and anticancer properties. Thimann and Bonner demonstrated that coumarin could inhibit the bending of slit internodes of P. sativum stem. The effects of coumarins have been attributed to several mechanisms, including acting as interferents mediating proteolytic metabolism or biosynthesis, cell cycle retarders that inhibit cell mitosis, disrupters of cellular redox homeostasis, and inhibitors of ATPases and electron transport, which can reduce respiration.
A series of coumarin derivatives with growth regulator effects have been developed and synthesized. One of these derivatives, 4-methylumbelliferone (4-MU), has been shown to be an effective regulator of lateral root formation. When exogenously applied to A. thaliana seeds, 4-MU affected the initial root growth, resulting in reduced primary root growth and the formation of abundant lateral roots. Besides, certain coumarin derivatives containing a benzoxazole ring, such as the 2-ethyl and 2-propyl substituted products, have been shown to exhibit inhibitory effects on the growth of lemon seedlings. In this sense, these derivatives have the potential to be applied as herbicides.
What Foods Are High in Dihydrocoumarin CAS 119-84-6?
In nature, coumarins can be found in a free form or conjugated with other molecules like glycosides. They are found in different parts of plants, such as roots, seeds, nuts, flowers and fruits of many species, being used as condiments (spices), herbal teas or medicines.
In addition, coumarins can also be found in some widely used foods like oils (olive), coffee, nuts, wine, and tea. Coumarins are even considered significant constituents of propolis that contribute to its pharmacological properties (esculin, daphnetin, fraxetin, umbelliferone, 4-methylumbelliferone, 4-hydroxycoumarin, scoparone, coumarin or herniarin).
What Is the Half Life of Dihydrocoumarin CAS 119-84-6?
Carbamazepine induces microsomal enzymes and shortens the plasma half-life of warfarin, lowers serum warfarin concentrations, and reduces the hypothrombinaemic effect under controlled conditions.
Discontinuing carbamazepine in one patient resulted in a potentially dangerous increase in prothrombin time.
Care should be taken to adjust warfarin dosage when stopping or starting carbamazepine in a patient stabilized on anticoagulants.
A male patient with a long-standing aortic valve replacement was receiving a weekly warfarin dose of 35 mg to maintain a target INR of 2.5 to 3.5. Monotherapy for seizures with felbamate (2400 mg/day) was started and raised to 3400mg/day after 2 weeks. Two weeks after felbamate was started his INR had increased to 7.5. Warfarin was therefore withheld for 3 days and restarted at a dose of 5 mg/day. Three weeks later the INR had risen to 18.2 and warfarin was withheld again for 4 days and restarted at a dose of 2.5 mg/day. The INR then stabilized within the target range. At no stage did the patient experience signs of bleeding. It was thought that felbamate had inhibited warfarin's metabolism.
Phenytoin may displace coumarins from plasma-binding sites and therefore potentiate their anticoagulant effect. Inhibition of coumarin metabolism increases their plasma half-life from 9 to 36 hr.
Dicoumarol inhibits the metabolism of phenytoin in the liver and thus potentiates its anticonvulsant effect; other coumarins may be expected to have this action, but not phenindione.
Coumarin was first isolated in 1820 from tonka beans and was also called Coumarou, a vernacular French name. Coumarins belong to a family of benzopyrones and are widely distributed in nature .
Coumarins can be found in seeds, fruits, flowers, roots, leaves, and stems of plants. They are secondary metabolites of higher plants and also a few microorganisms (bacteria and fungi) and sponges. Over 150 different species of different families that contain coumarins have been reported. They include Rutaceae, Umbelliferae, Clusiaceae, Guttiferae, Caprifoliaceae, Oleaceae, Nyctaginaceae, and Apiaceae . Regarding the chemical structure, coumarinic compounds are lactones resulting from the fusion of a benzene ring and a α-pyrone ring.
Coumarin is most often used as a fragrance ingredient, where it functions as a fragrance, as a fragrance enhancer, and as a stabilizer. Coumarin is widely used in perfumes, hand soaps, detergents, and lotions at concentrations from 0.01 to 2.4%. It is used to give pleasant aromas to household products or to mask unpleasant odors. The conservative estimate for systemic exposure of humans by using cosmetic products is 0.13 mg kg−1 day−1, disregarding any corrections that should be made for absorption that is <100%.
Coumarin is used as a pharmaceutical for the treatment of high-protein lymphedema and for improved venous circulation, and has been tested in clinical trials as an antineoplastic. Although coumarin's use in foods is allowed via naturals such as cinnamon, at the present time, coumarin is not permitted for use as a direct food additive; however, it is used as a tobacco flavor. Coumarin is also used in the electroplating industry.
Coumarin is used in the cosmetics industry as a fragrance in perfumes, shower gels, lotions or deodorants. The substance can be absorbed relatively easily through the skin and can thus lead to increased coumarin uptake when used regularly, especially in leave-on products such as perfumes. Due to its contact allergic properties, it is legally regulated in Regulation (EC) No. 1223/2009.
The presence of coumarin in cosmetic products must be indicated in the list of ingredients in addition to the indication of perfume or aroma mixtures or of herbal preparations from 0.01% in products that remain on the skin or from 0.001% in products that are washed off after application.
The use of derivatives of natural and synthetic origin has gained attention because of their therapeutic effects against human diseases. Coumarins are one of the most common organic molecules and are used in medicine for their pharmacological and biological effects, such as anti-inflammatory, anticoagulant, antihypertensive, anticonvulsant, antioxidant, antimicrobial, and neuroprotective, among others. In addition, coumarin derivates can modulate signaling pathways that impact several cell processes. The objective to provide a narrative overview of the use of coumarin-derived compounds as potential therapeutic agents, as it has been shown that substituents on the basic core of coumarin have therapeutic effects against several human diseases and types of cancer, including breast, lung, colorectal, liver, and kidney cancer.
In published studies, molecular docking has represented a powerful tool to evaluate and explain how these compounds selectively bind to proteins involved in various cellular processes, leading to specific interactions with a beneficial impact on human health. We also included studies that evaluated molecular interactions to identify potential biological targets with beneficial effects against human diseases.
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