22799-02-6

Post Buying Request

Basic information

Product Name: 20-HYDROXYECDYSONE 22-ACETATE
Synonyms: 2BETA,3BETA,14,20,22[R],25-HEXAHYDROXY-7-CHOLESTEN-6-ONE 22-ACETATE;20-HYDROXYECDYSONE 22-ACETATE;7-CHOLESTENE-2BETA,3BETA,14,20,22[R],25-HEXOL-6-ONE 22-ACETATE;7-Cholestene-2β,3β,14,20,22(R),25-hexol-6-one 22-acetate, 2β,3β,14,20,22(R),25-Hexahydroxy-7-cholesten-6-one 22-acetate;2β,3β,14,20,22(R),25-Hexahydroxy-7-cholesten-6-one 22-acetate;7-Cholestene-2β,3β,14,20,22(R),25-hexol-6-one 22-acetate
CAS NO:22799-02-6
Molecular Formula: C₂₉H₄₆O₈
Molecular Weight: 522.67
EINECS: N/A
Product Categories: Miscellaneous Natural Products
Mol File: 22799-02-6.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: 707.054°C at 760 mmHg
Flash Point: 226.851°C
Appearance: /
Density: 1.266g/cm³
Vapor Pressure: 0mmHg at 25°C
Refractive Index: 1.58
Storage Temp.: −20°C
Solubility: N/A
CAS DataBase Reference: 20-HYDROXYECDYSONE 22-ACETATE(CAS DataBase Reference)
NIST Chemistry Reference: 20-HYDROXYECDYSONE 22-ACETATE(22799-02-6)
EPA Substance Registry System: 20-HYDROXYECDYSONE 22-ACETATE(22799-02-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany: 3
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 22799-02-6(Hazardous Substances Data)

Suppliers
Usage
SDS
Upstream product
Downstream Products
Article

22799-02-6 Suppliers

Recommended suppliersmore

22799-02-6 Usage

Uses

20-Hydroxyecdysone 22-Acetate is used in the preparation of steroidal ligands and their use in gene switch modulation.

Check Digit Verification of cas no

The CAS Registry Mumber 22799-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22799-02:
(7*2)+(6*2)+(5*7)+(4*9)+(3*9)+(2*0)+(1*2)=126
126 % 10 = 6
So 22799-02-6 is a valid CAS Registry Number.

InChI:InChI=1/C29H46O8/c1-16(30)37-24(9-10-25(2,3)34)28(6,35)23-8-12-29(36)18-13-20(31)19-14-21(32)22(33)15-26(19,4)17(18)7-11-27(23,29)5/h13,17,19,21-24,32-36H,7-12,14-15H2,1-6H3/t17-,19-,21+,22-,23-,24+,26+,27+,28+,29+/m0/s1

22799-02-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	20-Hydroxyecdysone 22-acetate

1.2 Other means of identification

Product number	-
Other names	[(2R,3R)-2,6-dihydroxy-6-methyl-2-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl] acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22799-02-6 SDS

22799-02-6Upstream product

22799-02-6Downstream Products

22799-02-6Relevant articles and documents

Synthesis and biological activity of 2-deoxy-20-hydroxyecdysone and derivatives

Suksamrarn, Apichart,Yingyongnarongkul, Boon-Ek

, p. 12623 - 12630 (2007/10/03)

The naturally occurring ecdysteroids 2-deoxy-20-hydroxyecdysone (2-D-20-ECD, 2-deoxycrustecdysone), 2-D-20-ECD 3-acetate (2-deoxyecdysterone 3-acetate), 2-D-20-ECD 22-acetate and 2-D-20-ECD 22-benzoate have been partially synthesized from 20-hydroxyecdysone. Moulting hormone activity of these ecdysteroids has been studied using the Musca bioassay.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 22799-02-6