6BETA-HYDROXYTESTOSTERONE
- Product Name
- 6BETA-HYDROXYTESTOSTERONE
- CAS No.
- 62-99-7
- Chemical Name
- 6BETA-HYDROXYTESTOSTERONE
- Synonyms
- 6β-hydroxy Testosterone;Nsc 9721;6BETA-HYDROXYTESTOSERONE;Testosterone Impurity 11;6BETA-HYDROXYTESTOSTERONE;6β,17β-androst-4-en-3-one;6β-Hydroxytestosterone D7;D6-6β-Hydroxytestosterone;2H6]-6β-Hydroxytestosterone;4-Androsten-6b,17b-diol-3-one
- CBNumber
- CB4108083
- Molecular Formula
- C19H28O3
- Formula Weight
- 304.42
- MOL File
- 62-99-7.mol
6BETA-HYDROXYTESTOSTERONE Property
- Melting point:
- ≥205 °C
- Boiling point:
- 479.8±45.0 °C(Predicted)
- Density
- 1.19±0.1 g/cm3(Predicted)
- Flash point:
- 9℃
- storage temp.
- 2-8°C
- solubility
- Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml
- form
- A crystalline solid
- pka
- 13.98±0.70(Predicted)
- color
- white to off-white
Safety
- Hazard Codes
- Xn,T,F
- Risk Statements
- 61-40-39/23/24/25-23/24/25-11
- Safety Statements
- 53-22-36/37/39-45-36/37-16-7
- RIDADR
- UN1230 - class 3 - PG 2 - Methanol, solution
- WGK Germany
- 3
- HS Code
- 29372290
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H351Suspected of causing cancer
H360May damage fertility or the unborn child
- Precautionary statements
-
P201Obtain special instructions before use.
P202Do not handle until all safety precautions have been read and understood.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313IF exposed or concerned: Get medical advice/attention.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- H2898
- Product name
- 6β-Hydroxytestosterone
- Purity
- ≥97% (HPLC)
- Packaging
- 5mg
- Price
- $159.6
- Updated
- 2025/07/31
- Product number
- H-059
- Product name
- 6β-Hydroxytestosterone solution
- Purity
- 100?μg/mL in methanol, ampule of 1?mL, certified reference material, Cerilliant?
- Packaging
- 1mL
- Price
- $112
- Updated
- 2025/07/31
- Product number
- 10008519
- Product name
- 6β-hydroxy Testosterone
- Purity
- ≥97%
- Packaging
- 5mg
- Price
- $117
- Updated
- 2024/03/01
- Product number
- H2898
- Product name
- 6β-Hydroxytestosterone
- Purity
- ≥97% (HPLC)
- Packaging
- 25mg
- Price
- $578
- Updated
- 2025/07/31
- Product number
- SHG0007033
- Product name
- 6-BETA-HYDROXYTESTOSTERONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $786.5
- Updated
- 2021/12/16
6BETA-HYDROXYTESTOSTERONE Chemical Properties,Usage,Production
Description
CYP3A4 and CYP3A5 are cytochrome P450 enzymes whose expression is induced by glucocorticoids and certain xenobiotics, including many drugs and chemical carcinogens. They mediate the metabolism of xenobiotics as well as certain endobiotics, including steroid hormones. CYP3A4 and CYP3A5 are cytochrome P450 enzymes whose expression is induced by glucocorticoids and certain xenobiotics, including many drugs and chemical carcinogens. They mediate the metabolism of xenobiotics as well as certain endobiotics, including steroid hormones. 6β-
Chemical Properties
White Solid
Uses
A metabolite of Testosterone (T155000). CONTROLLED SUBSTANCE
Uses
A metabolite of Testosterone. CONTROLLED SUBSTANC
Definition
ChEBI: A 17beta-hydroxy steroid that is testosterone bearing an additional hydroxy substituent at the 6beta-position.
General Description
A Certified Spiking Solution? suitable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from clinical and diagnostic testing to endocrinology and sports testing. 6?-Hydroxytestosterone is a major urinary metabolite of testosterone, a hormone from the androgen group of steroids. Testosterone is an important sex hormone and anabolic steroid used as a performance-enhancing drug.
References
[1] BETH W COOPER. Phthalate induction of CYP3A4 is dependent on glucocorticoid regulation of PXR expression.[J]. Toxicological Sciences, 2008, 103 2: 268-277. DOI: 10.1093/toxsci/kfn047
[2] A J DRAPER. Development of a non-high pressure liquid chromatography assay to determine testosterone hydroxylase (CYP3A) activity in human liver microsomes.[J]. Drug Metabolism and Disposition, 1998, 26 4: 299-304.
[3] JORGE H. CAPDEVILA. Cytochrome P-450 enzyme-specific control of the regio- and enantiofacial selectivity of the microsomal arachidonic acid epoxygenase.[J]. The Journal of Biological Chemistry, 1990, 24 1: 10865-10871. DOI: 10.1016/s0021-9258(19)38526-6
[4] ATHAR HUSAIN . Herb–drug interaction studies of ethanolic extract of Cassia occidentalis L. coadministered with acetaminophen, theophylline, omeprazole, methotrexate and methylprednisolone[J]. Phytomedicine Plus, 2021, 1 1: Article 100008. DOI: 10.1016/j.phyplu.2020.100008
6BETA-HYDROXYTESTOSTERONE Preparation Products And Raw materials
Raw materials
Preparation Products
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