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ecdysone

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Origin: China

Cas No: 3604-87-3

Specification: 99%min

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  • Products Specification
  • Product Description
  • Property

    CAS No.: 3604-87-3 Formula: C27H44O6 Molecular Weight: 464.63500

    Description

    Ecdysone is a steroidal prohormone of the major insect molting hormone 20-hydroxyecdysone, which is secreted from the prothoracic glands. Insect molting hormones (ecdysone and its homologues) are generally called ecdysteroids. Ecdysteroids act as moulting hormones of arthropods but also occur in other related phyla where they can play different roles. In Drosophila melanogaster, an increase in ecdysone concentration induces the expression of genes coding for proteins that the larva requires, and it causes chromosome puffs (sites of high expression) to form in polytene chromosomes. Ecdysteroids also appear in many plants mostly as a protection agent (toxins or antifeedants) against herbivorous insects. These phytoecdysteroids have been reputed to have medicinal value and are part of herbal adaptogenic remedies like Cordyceps, yet an ecdysteroid precursor in plants has been shown to have cytotoxic properties. A pesticide sold with the name MIMIC has ecdysteroid activity, although its chemical structure has little resemblance to the ecdysteroids.

    Basic Info

    Chemical Name ecdysone
    Synonyms

    A-ECDYSONE;
    [3H]-Ecdysone;
    Ecdysone;
    (2β,3β,5β,22R)-2,3,14,22,25-pentahydroxycholest-7-en-6-one;
    Gynostemma Gypenosides;
    α-Ecdysone;

    CAS No. 3604-87-3
    Molecular Formula C27H44O6
    Molecular Weight 464.63500
    PSA 118.22000
    LogP 2.73910

    Properties

    Appearance & Physical State powder
    Density 1.22g/cm3
    Boiling Point 632ºC at 760mmHg
    Melting Point 242ºC
    Flash Point 350ºC
    Refractive Index 1.582
    Storage Condition 2-8ºC

    Safety Info

    RTECS FZ8170000
    Safety Statements S22-S24/25
    HS Code 2937290090
    WGK Germany 3

    Synthesis Route

    (2aS,4R,5S,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bR)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxooctadecahydro-1H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetateecdysone
    (2aS,4R,5S,6aR,6bR,8aS,8bR,9S,10R,11aS,12aR)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxo-2a,3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a,12,12a-hexadecahydro-2H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetateecdysone
    (2aS,4R,5S,6aR,6bR,8aR,8bR,9S,10R,11aS)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxo-2a,3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a-tetradecahydro-2H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetateecdysone

    Precursor

    (2aS,4R,5S,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bR)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxooctadecahydro-1H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetate
    (1S,2aS,4R,5S,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bR)-1-bromo-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxooctadecahydro-1H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetate
    (2aS,4R,5S,6aR,6bR,8aS,8bR,9S,10R,11aS,12aR)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxo-2a,3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a,12,12a-hexadecahydro-2H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetate
    (2aS,4R,5S,6aR,6bR,8aR,8bR,9S,10R,11aS)-10-(3-methoxy-3-oxopropyl)-6a,8a,9-trimethyl-2-oxo-2a,3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a-tetradecahydro-2H-naphtho[2',1':4,5]indeno[2,1-b]furan-4,5-diyl diacetate

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