80-33-1 MSDS - OVEX
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OVEX

Identification
Name OVEX
CAS Registry Number 80-33-1
Synonyms OVOTOX(R);OVOTRAN(R);OVATRAN;OVEX;P-CHLOROPHENYL-P-CHLOROBENZENE SULFONATE;ORTHOTRAN(R);MITRAN(R);(4-Chloor-fenyl)-4-chloor-benzeen-sulfonaat
Molecular Structure OVEX   80-33-1
Molecular Formula C12H8Cl2O3S
Molecular Weight 303.16
Hazard Codes: Details
Risk Statements: 22-38-50/53
Safety Statements: 37-60-61
RIDADR: UN3077 9/PG 3
Supplier
Lightchem Inc
Supply Precious metal catalyst
OLED Materials etc.
www.lightchem.com
 
Wiki & MSDS
80-33-1.pdf
Estrone
Estron.svg
Estrona3D.png
Clinical data
Routes of
administration
Intramuscular, vaginal
ATC code
  • G03CA07 (WHO)
    G03CC04 (WHO)
Legal status
Legal status
  • US: ℞-only
Pharmacokinetic data
Bioavailability Oral: Very low
Protein binding 96%:[1][2]
• Albumin: 80%
SHBG: 16%
• Free: 2–4%
Metabolism Liver (via hydroxylation, sulfation, glucuronidation)[1]
Biological half-life IV: 20–30 minutes[1]
Identifiers
CAS Number
  • 53-16-7 YesY
PubChem CID
  • 5870
IUPHAR/BPS
  • 2818
DrugBank
  • DB00655 N
ChemSpider
  • 5660 YesY
UNII
  • 2DI9HA706A
KEGG
  • D00067 N
ChEBI
  • CHEBI:17263 N
ChEMBL
  • CHEMBL1405 N
ECHA InfoCard 100.000.150
Chemical and physical data
Formula C18H22O2
Molar mass 270.366 g/mol
3D model (JSmol)
  • Interactive image
Melting point 254.5 °C (490.1 °F)
 NYesY (what is this?)  (verify)

Estrone (E1), also spelled oestrone, is a steroid, a weak estrogen, and a minor female sex hormone.[1] It is one of three major endogenous estrogens, the others being estradiol and estriol.[1] Estrone, as well as the other estrogens, are synthesized from cholesterol and secreted mainly from the gonads, though they can also be formed from adrenal androgens in adipose tissue.[3] Relative to estradiol, both estrone and estriol have far weaker activity as estrogens.[1] Previously, estrone was available as an injected estrogen for medical use, but it is now no longer marketed.[4]


 







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