• Product NameTestosterone undecanoate
  • CasNo. 5949-44-0
  • MFC30H48O3
  • MW456.709
  • Purity
  • AppearanceWhite crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 5949-44-0

MF: C30H48O3

Appearance: White crystalline powder

Perfect Factory Offer Excellent quality Testosterone undecanoate 5949-44-0 with Safe Shipping

  • Molecular Formula:C30H48O3
  • Molecular Weight:456.709
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:39-42°C(lit.) 
  • Refractive Index:1.522 
  • Boiling Point:550.7 °C at 760 mmHg 
  • Flash Point:230.3 °C 
  • PSA:43.37000 
  • Density:1.03 g/cm3 
  • LogP:7.96090 

Testosterone undecanoate(Cas 5949-44-0) Usage

Indications

JATENZO (testosterone undecanoate) is an androgen indicated for testosterone replacement therapy in adult males for conditions associated with a deficiency or absence of endogenous testosterone: Primary hypogonadism (congenital or acquired): testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, orchiectomy, Klinefelter syndrome, chemotherapy, or toxic damage from alcohol or heavy metals. These men usually have low serum testosterone concentrations and gonadotropins (follicle-stimulating hormone [FSH], luteinizing hormone [LH]) above the normal range. Hypogonadotropic hypogonadism (congenital or acquired): gonadotropin or luteinizing hormone-releasing hormone (LHRH) deficiency or pituitary-hypothalamic injury from tumors, trauma, or radiation. These men have low testosterone serum concentrations but have gonadotropins in the normal or low range.www.accessdata.fda.gov

Pharmacokinetics

Testosterone undecanoate is a prodrug of testos-terone esterified in the 17b-position with undecanoic acid. Following oral administration, thisprodrug is metabolized only partly in the intestinal wall, and the remaining fraction of testosterone undecanoate is absorbed via the lymphatic system, and hence, avoids first pass hepatic metabolism. After reaching the systemic circulation, testosterone undecanoate rapidly converts to free testosterone. The absolute bioavailability of testosterone following oral administration of testosterone undecanoate is estimated to be 7%. Recent studies in lymph duct cannulated dogs revealed that all of the testosterone undecanoate absorbed into the systemic circulation is due to lymphatic absorption of the prodrug, and more than 80% of the free testosterone in the plasma is contributed by systemic hydrolysis of the lymphatically transported prodrug.

Side effects

Side effects of testosterone undecanoate include symptoms of masculinization like acne, increased hair growth, voice changes, hypertension, elevated liver enzymes, hypertriglyceridemia, and increased sexual desire. The drug is a prodrug of testosterone, the biological ligand of the androgen receptor (AR) and hence is an androgen and anabolic steroid. It has strong androgenic effects and moderate anabolic effects, which make it useful for producing masculinization and suitable for androgen replacement therapy. Testosterone undecanoate is a testosterone ester and a prodrug of testosterone in the body. Because of this, it is considered to be a natural and bioidentical form of testosterone.

Definition

ChEBI: Testosterone undecanoate is a steroid ester. It is a metabolite of Testosterone. It is a promising androgen for male hormonal contraception.

InChI:InChI=1/C30H48O3/c1-4-5-6-7-8-9-10-11-12-28(32)33-27-16-15-25-24-14-13-22-21-23(31)17-19-29(22,2)26(24)18-20-30(25,27)3/h21,24-27H,4-20H2,1-3H3

5949-44-0 Relevant articles

Preparation method of alkyl acid testosterone

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Paragraph 0024-0025, (2020/11/10)

The invention discloses a preparation me...

Synthesis method of alkyl acid testosterone

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, (2020/12/10)

The invention discloses a synthesis meth...

Method for synthesizing alkyl-acid testosterone compound

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Paragraph 0024; 0025; 0026; 0027; 0028, (2016/10/10)

The invention provides a method for synt...

5949-44-0 Process route

undecanoyl chloride
17746-05-3

undecanoyl chloride

testosterone
58-22-0

testosterone

testosterone undecanoate
5949-44-0

testosterone undecanoate

Conditions
Conditions Yield
With pyridine; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 1h; Solvent; Reagent/catalyst; Inert atmosphere;
96%
With dmap; N-ethyl-N,N-diisopropylamine; In 1,2-dichloro-ethane; at 40 ℃;
13.5 g
undecanoyl chloride
17746-05-3

undecanoyl chloride

3,3-(ethylenedioxy)-5-androsten-17β-ol
975-57-5

3,3-(ethylenedioxy)-5-androsten-17β-ol

testosterone undecanoate
5949-44-0

testosterone undecanoate

Conditions
Conditions Yield
undecanoyl chloride; 3,3-(ethylenedioxy)-5-androsten-17β-ol; With dmap; triethylamine; In dichloromethane; at 20 ℃; Inert atmosphere;
With hydrogenchloride; In water;
96.15%

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