Chemical Properties of Hydroxyprogesterone Caproate (CAS 630-56-8)

Hydroxyprogesterone Caproate

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InChI
InChI=1S/C27H40O4/c1-5-6-7-8-24(30)31-27(18(2)28)16-13-23-21-10-9-19-17-20(29)11-14-25(19,3)22(21)12-15-26(23,27)4/h17,21-23H,5-16H2,1-4H3/t21-,22+,23+,25+,26+,27+/m0/s1
InChI Key
DOMWKUIIPQCAJU-UQSTXUIISA-N
Formula
C27H40O4
SMILES
CCCCCC(=O)OC1(C(C)=O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C
Molecular Weight1
428.60
CAS
630-56-8
Other Names
  • Pregn-4-ene-3,20-dione, 17-[(1-oxohexyl)oxy]-
  • Delalutin
  • Depo-proluton
  • Estralutin
  • Hormofort
  • Hydroxyprogesterone hexanoate
  • Hyproval
  • HPC
  • Kaprogest
  • Lutate
  • Neolutin forte
  • Pregn-4-ene-3,20-dione, 17-hydroxy-, hexanoate
  • Primolut Depot
  • Proge
  • Progesterone caproate
  • Progesterone, 17-hydroxy-, hexanoate
  • Proluton depot
  • Relutin
  • Syngynon
  • 17«alpha»-Hydroxyprogesterone caproate
  • 17«alpha»-Hydroxyprogesterone hexanoate
  • 17«alpha»-Hydroxyprogesterone n-caproate
  • Corlutin L.A.
  • Duraluton
  • 17-«alpha»-Hexanoyloxypregn-4-ene-3,20-dione
  • 17«alpha»-Hydroxypregn-4-ene-3,20-dione hexanoate
  • Hylutin
  • Hyproval-pa
  • Hyroxon
  • Idrogestene
  • Luteocrin
  • Luteocrin depot
  • Lutopron
  • Neolutin
  • NSC-17592
  • 17-((1-Oxohexyl)oxy)pregn-4-ene-3,20-dione
  • Progesterone retard pharlon
  • Teralutil
  • Gesterol LA 250
  • 17-Hydroxypregn-4-ene-3,20-dione caproate
  • Hyproval P.A.
  • Lewntogest
  • Pharlon
  • 3,20-Dioxopregn-4-en-17«alpha»-yl caproate
  • Hexanoic acid, ester with 17-hydroxypregn-4-ene-3,20-dione
  • 17«alpha»-Hydroxypregn-4-ene-3,20-dione caproate
  • Isoquinolinedione, 1,3(2h,4h)-, 2-hydroxy, acetate ester
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Physical Properties

Property Value Unit Source
Δf -138.03 kJ/mol Joback Calculated Property
Δfgas -783.94 kJ/mol Joback Calculated Property
Δfus 35.70 kJ/mol Joback Calculated Property
Δvap 93.24 kJ/mol Joback Calculated Property
log10WS -6.88 Crippen Calculated Property
logPoct/wat 5.970 Crippen Calculated Property
McVol 354.130 ml/mol McGowan Calculated Property
Pc 1164.04 kPa Joback Calculated Property
Tboil 1058.97 K Joback Calculated Property
Tc 1306.11 K Joback Calculated Property
Tfus 715.02 K Joback Calculated Property
Vc 1.351 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1391.28; 1687.22] J/mol×K [1058.97; 1306.11] Show Hide
Cp,gas 1391.28 J/mol×K 1058.97 Joback Calculated Property
Cp,gas 1432.03 J/mol×K 1100.16 Joback Calculated Property
Cp,gas 1475.54 J/mol×K 1141.35 Joback Calculated Property
Cp,gas 1522.32 J/mol×K 1182.54 Joback Calculated Property
Cp,gas 1572.86 J/mol×K 1223.73 Joback Calculated Property
Cp,gas 1627.66 J/mol×K 1264.92 Joback Calculated Property
Cp,gas 1687.22 J/mol×K 1306.11 Joback Calculated Property

Similar Compounds

17Alpha-acetoxy-6alpha-methyl-pregn-4-ene-3,20-dione. Medroxyprogesterone acetate. 17«alpha»,21-Dihydroxypregn-4-en-3,20-dione, 17,21-anhydro (oxetanone). methyltestosterone acetate. 10A,12a-dimethyl-3,4,4a,5,6,9,10,10a,10b,11,12,12a-dodecahydro-2h-naphtho[2,1-f]chromene-2,8(4bh)-dione. Pregn-4-ene-3,20-dione, 16,17-epoxy-, (16«alpha»)-. Epitestosterone, hexanoate. Epitestosterone, octanoate. Epitestosterone, butyrate. Testosterone Decanoate. Testosterone enanthate. Megestrol acetate. Androst-4-ene-16beta-proionic acid, 17beta-hydroxy-3-oxo-, delta-lactone. Testosterone cypionate. Epitestosterone, propionate.

Find more compounds similar to Hydroxyprogesterone Caproate.

Sources

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