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58-20-8

Basic Information
CAS No.: 58-20-8
Name: Androst-4-en-3-one,17-(3-cyclopentyl-1-oxopropoxy)-, (17b)-
Molecular Structure:
Molecular Structure of 58-20-8 (Androst-4-en-3-one,17-(3-cyclopentyl-1-oxopropoxy)-, (17b)-)
Formula: C27H40O3
Molecular Weight: 412.61
Synonyms: Testosterone,cyclopentanepropionate (6CI,7CI,8CI);Cyclopentanepropionic acid, ester withtestosterone (8CI);17b-Hydroxyandrost-4-en-3-one cyclopentanepropionate;DepAndro 100;DepAndro 200;Depo-testosterone;Depotest;Depovirin;NSC 9157;Pertestis;Testex Leo;Testodrinprolongatum;Testosterone 17b-cyclopentanepropionate;Testosterone 17b-cypionate;Testosterone cyclopentylpropionate;Testosterone cypionate;Testosterone, 3-cyclopentanepropionate;Virilon;
EINECS: 200-368-4
Density: 1.1 g/cm3
Melting Point: 98 - 104ºC
Boiling Point: 525.9 °C at 760 mmHg
Flash Point: 223.9 °C
Solubility:
Appearance: white to off-white crystalline powder
Hazard Symbols: ToxicT
Risk Codes: 45-63
Safety: 53-22-26-36
Transport Information:
PSA: 43.37000
LogP: 6.40050
Synthetic route
104-97-2

cyclopentanepropanoyl chloride

58-22-0

testosterone

58-20-8

testosterone cypionate

Conditions
ConditionsYield
With pyridine In N,N-dimethyl acetamide at 0 - 20℃; for 5h; Inert atmosphere;77%
58-22-0

testosterone

58032-37-4

3-cyclopentyl-propionic acid-anhydride

58-20-8

testosterone cypionate

17β-(3-cyclopentyl-propionyloxy)-androst-5-en-3β-ol

58-20-8

testosterone cypionate

Conditions
ConditionsYield
With lithium tetra(iso-propoxo)aluminate; cyclohexanone
56736-66-4

3-ethoxy-17β-(3-cyclopentyl-propionyloxy)-androsta-3,5-diene

58-20-8

testosterone cypionate

Conditions
ConditionsYield
With hydrogenchloride; acetone
140-77-2

3-cyclopentylpropionic acid

58-20-8

testosterone cypionate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: acetic acid anhydride
View Scheme
Multi-step reaction with 3 steps
1: acetic acid anhydride
3: aqueous HCl; acetone
View Scheme
58032-37-4

3-cyclopentyl-propionic acid-anhydride

58-20-8

testosterone cypionate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: aqueous HCl; acetone
View Scheme
17006-07-4, 38394-98-8, 77881-13-1

17-hydroxy-3-oxo-androst-4-ene-17-carbonitrile

58-20-8

testosterone cypionate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Edukt 1: aus Androst-4-en-3,17-dion
View Scheme
58-20-8

testosterone cypionate

58-22-0

testosterone

Conditions
ConditionsYield
With water In methanol at 40℃; Rate constant; pH 9, also reaction in the presence of 2-hydroxypropyl-β-cyclodextrin;
In ethanol; water at 37℃; Product distribution; Hydrolysis;
With Novozyme 51032 In aq. phosphate buffer at 20℃; for 20h; pH=8; Enzymatic reaction;
356-42-3

2,2,3,3,3-pentafluoropropanoic anhydride

58-20-8

testosterone cypionate

2,2,3,3,3-Pentafluoro-propionic acid (8R,9S,10R,13S,14S,17S)-17-(3-cyclopentyl-propionyloxy)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Conditions
ConditionsYield
at 70℃; for 0.25h;
24589-78-4

N-methyl-N-trimethylsilyl-2,2,2-trifluoroacetamide

58-20-8

testosterone cypionate

3-Cyclopentyl-propionic acid (8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-trimethylsilanyloxy-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl ester

Conditions
ConditionsYield
With ammonium iodide; 1,4-dithio-erythritol at 60℃; for 0.25h;
58-20-8

testosterone cypionate

407-25-0

trifluoroacetic anhydride

3-Cyclopentyl-propionic acid (8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-(2,2,2-trifluoro-acetoxy)-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl ester

Conditions
ConditionsYield
at 70℃; for 0.25h;
58-20-8

testosterone cypionate

336-59-4

heptafluorobutyric anhydride

2,2,3,3,4,4,4-Heptafluoro-butyric acid (8R,9S,10R,13S,14S,17S)-17-(3-cyclopentyl-propionyloxy)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Conditions
ConditionsYield
at 70℃; for 0.25h;
Downstream Products
58-22-0
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Specification

The IUPAC name of Testosterone cyclopentylpropionate is (10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) 3-cyclopentylpropanoate. With the CAS registry number 58-20-8, it is also named as Testosterone 17beta-cypionate. The classification codes are Anabolic Agents; Androgen; Androgens; Hormone; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Human Data; Mutation data; Reproductive Effect. When heated to decomposition it emits acrid smoke and irritating fumes. Additionally, it is steroids which is used as androgen. And this chemical must be stored at 2-8°C.

The other characteristics of this product can be summarized as: (1)ACD/LogP: 6.93; (2)# of Rule of 5 Violations: 1; (3)#H bond acceptors: 3; (4)#H bond donors: 0; (5)#Freely Rotating Bonds: 5; (6)Index of Refraction: 1.546; (7)Molar Refractivity: 118.41 cm3; (8)Molar Volume: 373.8 cm3; (9)Polarizability: 46.94×10-24 cm3; (10)Surface Tension: 43.7 dyne/cm; (11)Enthalpy of Vaporization: 80.01 kJ/mol; (12)Vapour Pressure: 3.78E-11 mmHg at 25°C; (13)Rotatable Bond Count: 5; (14)Tautomer Count: 5; (15)Exact Mass: 412.297745; (16)MonoIsotopic Mass: 412.297745; (17)Topological Polar Surface Area: 43.4; (18)Heavy Atom Count: 30; (19)Complexity: 732.

When you are using Testosterone cyclopentylpropionate, please be cautious about it as the following:
It may cause cancer and possible risk of harm to the unborn child, so people should not breathe dust. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing. Avoid exposure - obtain special instructions before use.

People can use the following data to convert to the molecule structure.
1. SMILES:O=C5\C=C3/[C@]([C@H]2CC[C@@]4([C@@H](OC(=O)CCC1CCCC1)CC[C@H]4[C@@H]2CC3)C)(C)CC5
2. InChI:InChI=1/C27H40O3/c1-26-15-13-20(28)17-19(26)8-9-21-22-10-11-24(27(22,2)16-14-23(21)26)30-25(29)12-7-18-5-3-4-6-18/h17-18,21-24H,3-16H2,1-2H3/t21-,22-,23-,24-,26-,27-/m0/s1.

The following is the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal > 1gm/kg (1000mg/kg)   Drugs in Japan Vol. 6, Pg. 487, 1982.