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Detail of "482-44-0"

  • CAS Number:
  • 482-44-0
  • Name:
  • Imperatorin

  • Molecular Structure:
  • Formula:
  • C16H14O4
  • Molecular Weight:
  • 270.28
  • Deleted CAS:
  • 70102-00-0
  • Synonyms:
  • 7H-Furo[3,2-g][1]benzopyran-7-one,9-[(3-methyl-2-butenyl)oxy]- (8CI,9CI);Imperatorin (6CI);8-Isopent-2-enyloxy-6,7-furanocoumarin;8-Isopentenyloxypsoralene;Ammidin;Marmelide;Marmelosin;NSC 402949;7H-Furo[3,2-g][1]benzopyran-7-one,9-[(3-methyl-2-buten-1-yl)oxy]-;9-[(3-Methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g]chromen-7-one;
  • EINECS:
  • 207-581-1
  • Density:
  • 1.243 g/cm3
  • Melting Point:
  • 98-100 °C
  • Boiling Point:
  • 448.319 °C at 760 mmHg
  • Flash Point:
  • 224.936 °C
  • Solubility:
  • Soluble in chloroform, benzene, ethanol, ethyl ether and caustic alkali solutions, insoluble in cold water
  • Appearance:
  • white solid

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CAS No.482-44-0 ImperatorinCompetitive Product

Assay:95%HPLC  Package:1g; 100g;1kgStorage:Store in dry...  Application:Analytical S...

Imperatorin

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CAS No.482-44-0 Imperatorin

Assay:98%HPLC  Appearance:fine powder  Package:67 kg/vacuum...Storage:store in a c...  Transportation:Air courier ...  Application:medicine add...

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CAS No.482-44-0 Imperatorin

Assay:97.00%  Appearance:powder or cr...  Package:10mg,20mg,1g...Storage:-20degree

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CAS No.482-44-0 Imperatorin

Assay:HPLC≥98%

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CAS No.482-44-0 Imperatorin

Product name:Imperatorin CAS NO: 482-44-0 Assay:98% Solubility:Soluble in chloroform Appearance:Offwhite powder Usages:sedative, antispasmodic, anti-asthma, anti-inflammatory, antibacterial effect

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CAS No.482-44-0 Imperatorin

[English Name]:Imperatorin [Origin]:Drynaria heraclea Kze [Detection]:HPLC [Purity]:99% [Molecule formula]:C16H14O4 [Molecule weight]:270.2799 [Appearance]: White powder [CAS No]:482-44-0 [Use]:Quantitative analysis

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Imperatorin cas:482-44-0 HPLC≥98% 20mg

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CAS No.482-44-0 Imperatorin

Product name:Imperatorin CAS: 482-44-0 Molecular formula:C16H14O4 Molecular mass:270.28

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[Name]Imperatorin [Assay]+98% [CasNo]482-44-0 [Pack]100mg.1g .10g

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Reference

Biological actions of the natural coumarins
Biological actions of the natural coumarins. I. Changes of lipids and glucose levels in rat plasma after intraperitoneal administration of various linear-type furanocoumarins. Yasuda, Masahide; Baba, Kimiye; Kozawa, Mitsugi (Osaka Coll. Pharm., Osaka 580, Japan). Chem. Pharm. Bull., 32(11), 4650-2 (English) 1984. CODEN: CPBTAL. ISSN: 0009-2363. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Expts. were carried out on the effect of various linear-type furanocoumarins on the concns. of lipids and glucose in rat plasma. It was found that bergapten (I) [484-20-8] and xanthotoxin [298-81-7] cause hypolipidemia. In contrast, imperatorin [482-44-0], isoimperatorin [482-45-1], oxypeucedanin (II) [26091-73-6] and oxypeucedanin hydrate [2643-85-8] cause hyperlipidemia. However, no effect on any lipid fraction in rat plasma was produced by isopimpinellin [482-27-9], phellopterin [2543-94-4], ferulin [29455-13-8], byakangelicin [482-25-7] or sec-O-acetylbyakangelicin [77196-05-5]. Glucose levels in rat plasma were increased by isopimpinellin and psoralen [66-97-7], and decreased by oxypeucedanin. These results suggest that the effects of linear-type furanocoumarin on lipid concn. in rat plasma depend upon whether substitution is present or not at the 5- and 8-posiiton of the skeleton and upon the kinds of substituents.
Fluorometric analysis of furocoumarins
Fluorometric analysis of furocoumarins. Hilal, S. H.; Radwan, A. S.; Haggag, M. Y.; Melek, F. R.; Abdel Khalek, S. M. (Lab. Nat. Prod., NRC, Egypt). Egypt. J. Pharm. Sci., Volume Date 1982, 23(1-4), 365-70 (English) 1984. CODEN: EJPSBZ. ISSN: 0301-5068. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Bergapten (I) [484-20-8], imperatorin (II) [482-44-0], and xanthotoxin (III) [298-81-7] were sepd. in Ammi majus ext. by TLC and detected by fluorometry. The ext. was chromatographed using silica gel G impregnated with 10% HCONH2 in MeOH as stationary phase and hexane-benzene-MeOH 7:2:1 as eluting system. The spots were outlined under UV light (254 nm) against stds. II and III can be detd. in a concn. range of 2-20 and 2-15 mg, resp., and I at 5-15 mg. The method was also applied to pharmaceutical tablets contg. 5 mg II and 10 mg III. The method is more rapid and highly sensitive compared to traditional methods.
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