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SML3731

Sigma-Aldrich

Testosterone undecanoate

≥98% (HPLC)

Synonym(s):

(17β)-17-[(1-Oxoundecyl)oxy]androst-4-en-3-one, Undecanoic acid ester with testosterone

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About This Item

Empirical Formula (Hill Notation):
C30H48O3
CAS Number:
5949-44-0
Molecular Weight:
456.70
MDL number:
MFCD00468114
UNSPSC Code:
51111800
UNSPSC Code:
12352200
NACRES:
NA.24

Quality Level

100

Assay

≥98% (HPLC)

form

powder

drug control

USDEA Schedule III

color

white to beige

solubility

DMSO: 2 mg/mL, clear (Warmed)

storage temp.

-10 to -25°C

Biochem/physiol Actions

Testosterone undecanoate is an orally available prodrug of testosterone that has a very long elimination half-life. It is an androgen and anabolic–androgenic steroid that acts as agonist of the androgen receptor (AR). Testosterone undecanoate is mainly used in the treatment of low testosterone levels in men. Also, it was approved for treatment of male hypogonadism.

Signal Word

Danger

Hazard Statements

H302,H351,H360FD,H400

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Carc. 2 - Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Contribution of lymphatically transported testosterone undecanoate to the systemic exposure of testosterone after oral administration of two andriol formulations in conscious lymph duct-cannulated dogs
Journal of Pharmacology and Experimental Therapeutics, 306(3), 925-933 (2003)
Testosterone undecanoate and testosterone enanthate injections are both effective and safe in transmen over 5 years of administration
Clinical Endocrinology, 89(6), 878-886 (2018)
Atheer Zgair et al.
Molecules (Basel, Switzerland), 26(1) (2021-01-21)
Male hypogonadism is often treated by testosterone (T) replacement therapy such as oral administration of the ester prodrug, testosterone undecanoate (TU). However, the systemic exposure to T following oral TU is very low due to esterase-mediated metabolism, particularly in the

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