ANDROSTENEDIOL-3-ACETATE
ANDROSTENEDIOL-3-ACETATE
CAS: 1639-43-6
Molecular Formula: C21H32O3
ANDROSTENEDIOL-3-ACETATE - Names and Identifiers
ANDROSTENEDIOL-3-ACETATE - Physico-chemical Properties
| Molecular Formula | C21H32O3 |
| Molar Mass | 332.48 |
| Density | 1.12±0.1 g/cm3(Predicted) |
| Melting Point | 147-148° |
| Boling Point | 436.8±45.0 °C(Predicted) |
| pKa | 15.04±0.70(Predicted) |
| Storage Condition | 2-8℃ |
ANDROSTENEDIOL-3-ACETATE - Introduction
ANDROSTENEDIOL-3-ACETATE (androstanol -3-acetate) is a synthetic androgenic compound with a variety of properties and uses.
Nature:
-Physical properties: ANDROSTENEDIOL-3-ACETATE is a white crystalline solid, sometimes it is a colorless or slightly yellow liquid, with a special smell.
-Chemical properties: It is a derivative of androgen, which can be esterified with acetic acid through an ester bond. It can be hydrolyzed in the body by esterases to androtriol, a more biologically active compound.
Use:
-medical applications: ANDROSTENEDIOL-3-ACETATE used for the treatment of testicular dysfunction, loss of libido and other male sexual dysfunction. It can also be used to increase estrogen levels in women to promote breast development.
-Laboratory research: ANDROSTENEDIOL-3-ACETATE is commonly used in laboratory research to study the biological effects of androgen, metabolic pathways, etc.
Method:
The preparation of ANDROSTENEDIOL-3-ACETATE can be synthesized by Jessen side reaction. First, androtriol is reacted with the acylating reagent acetic anhydride under acidic conditions to form ANDROSTENEDIOL-3-ACETATE.
Safety Information:
Although ANDROSTENEDIOL-3-ACETATE is a synthetic compound, it is usually relatively safe under proper use and storage conditions. However, it is still an androgen with potential sex hormone effects and toxicity. Therefore, when using, it is necessary to use it in accordance with the correct dosage and guidance, and pay attention to avoid contact with children and pregnant women. In addition, users should also take care to protect their personal protection, avoid inhalation of aerosols or skin contact, and follow appropriate laboratory safety procedures.
Nature:
-Physical properties: ANDROSTENEDIOL-3-ACETATE is a white crystalline solid, sometimes it is a colorless or slightly yellow liquid, with a special smell.
-Chemical properties: It is a derivative of androgen, which can be esterified with acetic acid through an ester bond. It can be hydrolyzed in the body by esterases to androtriol, a more biologically active compound.
Use:
-medical applications: ANDROSTENEDIOL-3-ACETATE used for the treatment of testicular dysfunction, loss of libido and other male sexual dysfunction. It can also be used to increase estrogen levels in women to promote breast development.
-Laboratory research: ANDROSTENEDIOL-3-ACETATE is commonly used in laboratory research to study the biological effects of androgen, metabolic pathways, etc.
Method:
The preparation of ANDROSTENEDIOL-3-ACETATE can be synthesized by Jessen side reaction. First, androtriol is reacted with the acylating reagent acetic anhydride under acidic conditions to form ANDROSTENEDIOL-3-ACETATE.
Safety Information:
Although ANDROSTENEDIOL-3-ACETATE is a synthetic compound, it is usually relatively safe under proper use and storage conditions. However, it is still an androgen with potential sex hormone effects and toxicity. Therefore, when using, it is necessary to use it in accordance with the correct dosage and guidance, and pay attention to avoid contact with children and pregnant women. In addition, users should also take care to protect their personal protection, avoid inhalation of aerosols or skin contact, and follow appropriate laboratory safety procedures.
Last Update：2024-04-09 21:01:54
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Product Name: ANDROSTENEDIOL-3-ACETATE Visit Supplier Webpage Request for quotation
CAS: 1639-43-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 1639-43-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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