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T1875

Testosterone propionate

solid

Synonyme(s) :

17β-hydroxy-4-androstène-3-one 17-propionate, 4-androstène même-17β-ol-3-one 17-propionate

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A propos de cet article

Formule empirique (notation de Hill) :
C22H32O3
Numéro CAS:
Poids moléculaire :
344.49
UNSPSC Code:
51111800
NACRES:
NA.77
PubChem Substance ID:
EC Number:
200-351-1
Beilstein/REAXYS Number:
3221760
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Quality level:
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biological source

synthetic (organic)

Quality Level

sterility

non-sterile

assay

≥98% (HPLC)

form

solid

drug control

USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

color

white

solubility

acetone: soluble 1 in 4 of acetone, chloroform: soluble 50 mg/ml, clear, colorless to faintly yellow, ethanol: soluble 1 in 6 of ethanol, ethyl oleate: soluble 1 in 20 of ethyl oleate, propylene glycol: soluble 1 in 30 of propylene glycol, soluble 1 in 20 of ethyl oleate, ethanol: 10 mg/mL, 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 4.4 mg/mL, H2O: insoluble, oil: soluble

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])OC(=O)CC

InChI

1S/C22H32O3/c1-4-20(24)25-19-8-7-17-16-6-5-14-13-15(23)9-11-21(14,2)18(16)10-12-22(17,19)3/h13,16-19H,4-12H2,1-3H3/t16-,17-,18-,19-,21-,22-/m0/s1

InChI key

PDMMFKSKQVNJMI-BLQWBTBKSA-N

Gene Information

human ... AR(367), CYP17A1(1586)
rat ... Ar(24208)

Application

Testosterone propionate has been used for studying its effects on pregnant ewes[1],[2].

Biochem/physiol Actions

Androgens direct the development of the male phenotype during embryogenesis and at puberty. Testosterone is an androgen that is secreted by the testis. This hormone is converted to dihydrotestosterone in the target tissues where it regulates several biological functions. Testosterone propionate has been synthetically derived from a plant. This product has extended and faster-acting functions when compared to other testosterone esters.

Physical form

Photosensitive solid

Preparation Note

This product is soluble in chloroform (50 mg/ml). It is also soluble in various oils. The oil solutions can be sterilized by maintaining at 150 deg C for 1 hour. It is practically insoluble in water, soluble 1 in 6 of ethanol, 1 in 4 of acetone, 1 in 20 of ethyl oleate, and 1 in 30 of propylene glycol. The product is incompatible with alkalis and oxidizing agents and it should be protected from light.

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Cet article
86541PHR2026Y0001409
form

solid

form

solid

form

solid

form

-

assay

≥98% (HPLC)

assay

-

assay

-

assay

-

drug control

USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

drug control

USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada

drug control

-

drug control

-

Quality Level

200

Quality Level

-

Quality Level

300

Quality Level

-

storage temp.

room temp

storage temp.

-

storage temp.

2-30°C

storage temp.

2-8°C

solubility

acetone: soluble 1 in 4 of acetone, ethanol: soluble 1 in 6 of ethanol, propylene glycol: soluble 1 in 30 of propylene glycol, ethanol: 10 mg/mL, H2O: insoluble, chloroform: soluble 50 mg/ml, clear, colorless to faintly yellow, soluble 1 in 20 of ethyl oleate, oil: soluble, ethyl oleate: soluble 1 in 20 of ethyl oleate, 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 4.4 mg/mL

solubility

-

solubility

-

solubility

-


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Danger

Hazard Classifications

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

Classe de stockage

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

wgk

WGK 3

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges



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Contenu apparenté

Product Information Sheet


M E Rose et al.
Infection and immunity, 26(2), 630-637 (1979-11-01)
Comparisons were made between infections with Eimeria spp. in normal animals and in animals with functional deficiencies in either T-lymphocytes (athymic nude rats) or B-lymphocytes (bursectomized chickens). Approximately three times more oocysts of E. nieschulzi were passed during a primary
Maria Cernea et al.
Endocrinology, 156(9), 3277-3291 (2015-06-11)
Prenatal testosterone (T)-treated ewes display a constellation of reproductive defects that closely mirror those seen in PCOS women, including altered hormonal feedback control of GnRH. Kisspeptin/neurokinin B/dynorphin (KNDy) neurons of the arcuate nucleus (ARC) play a key role in steroid
Tsuyoshi Shimmura et al.
Scientific reports, 9(1), 3978-3978 (2019-03-10)
Animals that communicate using sound are found throughout the animal kingdom. Interestingly, in contrast to human vocal learning, most animals can produce species-specific patterns of vocalization without learning them from their parents. This phenomenon is called innate vocalization. The underlying



Numéro d'article de commerce international

RéférenceGTIN
T1875-5G04061837338304
T1875-1G04061826694503
T1875-100G04061837338298

Questions

  1. Is T1875 suitable for in vivo application?

    1 réponse
    1. The use of T1875 for in vivo application was discussed and cited in the following article as a protocol reference: J Neuroendocrinol. 2015 Feb; 27(2): 100–110. The article is titled "Prenatal Testosterone Excess Decreases Neurokinin 3 Receptor Immunoreactivity within the Arcuate Nucleus KNDy cell population" with the PMID: 25496429.

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