6626-42-2 Usage
Synonyms
Estra-1,3,5(10)-triene-3,6alpha,17beta-triol triacetate
Chemical class
Synthetic derivative of the hormone estrogen
Molecular structure
Steroid compound with three acetyl ester groups attached to the hydroxyl (OH) groups at the 3, 6, and 17 positions
Research
Studying estrogen receptor binding and activity
Pharmaceutical
Potential therapeutic applications in hormone replacement therapy or treatment of conditions related to hormone imbalance
Quality control
Reference standard for analytical testing in the pharmaceutical industry
Functional groups
Acetyl ester groups, hydroxyl groups
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetonitrile
Stability
Stable under normal temperature and pressure conditions, but sensitive to light, heat, and moisture
Safety precautions
Handle with care, use appropriate personal protective equipment (PPE), and follow proper disposal procedures to minimize environmental impact and health risks
Purity
Typically available at high purity levels (e.g., ≥95% or ≥98%)
Analytical techniques
Can be analyzed and identified using techniques such as mass spectrometry (MS), nuclear magnetic resonance (NMR), and infrared (IR) spectroscopy
Regulatory status
May be subject to specific regulations depending on the intended use and region, such as the US Food and Drug Administration (FDA) or the European Medicines Agency (EMA) guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 6626-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6626-42:
(6*6)+(5*6)+(4*2)+(3*6)+(2*4)+(1*2)=102
102 % 10 = 2
So 6626-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H30O6/c1-13(25)28-16-5-6-17-18-9-10-24(4)21(7-8-23(24)30-15(3)27)19(18)12-22(20(17)11-16)29-14(2)26/h5-6,11,18-19,21-23H,7-10,12H2,1-4H3/t18-,19-,21+,22+,23+,24+/m1/s1
