E9004
α-Ecdysone
≥90%
Synonym(s):
2β,3β,14α,22(R),25-Pentahydroxy-7-cholesten-6-one
About This Item
Recommended Products
sterility
non-sterile
Quality Level
Assay
≥90%
form
powder
solubility
methanol: 20 mg/mL, clear, colorless to faintly yellow
application(s)
agriculture
environmental
shipped in
ambient
storage temp.
−20°C
SMILES string
[H][C@]12CC[C@]3(C)[C@H](CC[C@@]3(O)C1=CC(=O)[C@]4([H])C[C@@H](O)[C@@H](O)C[C@]24C)[C@H](C)[C@H](O)CCC(C)(C)O
InChI
1S/C27H44O6/c1-15(20(28)8-9-24(2,3)32)16-7-11-27(33)18-12-21(29)19-13-22(30)23(31)14-25(19,4)17(18)6-10-26(16,27)5/h12,15-17,19-20,22-23,28,30-33H,6-11,13-14H2,1-5H3/t15-,16+,17-,19-,20+,22+,23-,25+,26+,27+/m0/s1
InChI key
UPEZCKBFRMILAV-JMZLNJERSA-N
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General description
Application
- to study its effects on Drosophila melanogaster′s sexual maturation
- to study its effects on specification of neurons in Drosphila male-specific neurite
- as a standard to evaluate the ecdysteroid levels by liquid chromatography-mass spectrometry (LC-MS/MS)
Biochem/physiol Actions
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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