80-75-1

  • Product Name:11Α-Hydroxyprogesterone
  • Molecular Formula:C21H30O3
  • Purity:99%
  • Molecular Weight:330.467
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Product Details;

CasNo: 80-75-1

Molecular Formula: C21H30O3

Appearance: white to light beige crystalline powder

Buy High Quality Top Purity 11Α-Hydroxyprogesterone 80-75-1 Low Price

  • Molecular Formula:C21H30O3
  • Molecular Weight:330.467
  • Appearance/Colour:white to light beige crystalline powder 
  • Vapor Pressure:1.51E-11mmHg at 25°C 
  • Melting Point:165-166 °C 
  • Refractive Index:1.557 
  • Boiling Point:487.4 °C at 760 mmHg 
  • PKA:14.52±0.70(Predicted) 
  • Flash Point:262.7 °C 
  • PSA:54.37000 
  • Density:1.15 g/cm3 
  • LogP:3.69430 

11ALPHA-HYDROXYPROGESTERONE(Cas 80-75-1) Usage

Chemical Properties

white to light beige crystalline powder

Uses

Progesterone (P755900) metabolite.

Definition

ChEBI: A 11alpha-hydroxy steroid that is pregn-4-ene-3,20-dione substituted by a hydroxy group at position 11.

InChI:InChI=1/C21H30O3/c1-12(22)16-6-7-17-15-5-4-13-10-14(23)8-9-20(13,2)19(15)18(24)11-21(16,17)3/h10,15-19,24H,4-9,11H2,1-3H3/t15-,16?,17-,18+,19+,20-,21+/m0/s1

80-75-1 Relevant articles

Dehalogenation methodof 9-halogenated steroid compound and application

-

Paragraph 0197-0199, (2021/01/11)

The invention provides a dehalogenation ...

Biotransformation of progesterone by Aspergillus nidulans VKPM F-1069 (wild type)

Savinova, Olga S.,Solyev, Pavel N.,Vasina, Daria V.,Tyazhelova, Tatiana V.,Fedorova, Tatiana V.,Savinova, Tatiana S.

, (2019/06/25)

Biotechnological transformation of stero...

Biotransformation of progesterone by the ascomycete Aspergillus niger N402

Savinova,Solyev,Vasina,Tyazhelova,Fedorova,Savinova

, p. 26 - 31 (2018/02/06)

The ability of the ascomyceteAspergillus...

Engineering of CYP106A2 for steroid 9α- and 6β-hydroxylation

Nikolaus, Julia,Nguyen, Kim Thoa,Virus, Cornelia,Riehm, Jan L.,Hutter, Michael,Bernhardt, Rita

, p. 41 - 48 (2017/03/17)

CYP 106A2 from Bacillus megaterium ATCC ...

80-75-1 Process route

Progesterone
57-83-0

Progesterone

pregnan-3-ol-20-one

pregnan-3-ol-20-one

pregnane-3,20-diol
4479-11-2

pregnane-3,20-diol

4-pregnen-20α-ol-3-one
15114-79-1

4-pregnen-20α-ol-3-one

14-hydroxy-4-pregnene-3,20-dione
16031-66-6

14-hydroxy-4-pregnene-3,20-dione

dihydroprogesterone
566-65-4

dihydroprogesterone

11-alpha-hydroxyprogesterone
80-75-1,22847-91-2

11-alpha-hydroxyprogesterone

6alpha-Hydroxyprogesterone
604-20-6

6alpha-Hydroxyprogesterone

Conditions
Conditions Yield
With Hortaea werneckii B-763 at early logarithmic growth phase; In YNB growth medium; N,N-dimethyl-formamide; at 28 ℃; for 24h; Enzymatic reaction;
 
3,20-dioxopregn-4-en-11α-yl Se-phenyl selenocarbonate

3,20-dioxopregn-4-en-11α-yl Se-phenyl selenocarbonate

Progesterone
57-83-0

Progesterone

11-alpha-hydroxyprogesterone
80-75-1,22847-91-2

11-alpha-hydroxyprogesterone

3,20-dioxopregn-4-en-11α-yl formate
115459-64-8

3,20-dioxopregn-4-en-11α-yl formate

Conditions
Conditions Yield
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In xylene; at 144 ℃;
8%
3%
83%

80-75-1 Upstream products

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    2402-20-2

    11α-acetoxy-5α-pregnane-3,20-dione

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80-75-1 Downstream products

  • 565-96-8
    565-96-8

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  • 565-94-6
    565-94-6

    11α-hydroxy-5β-pregnane-3,20-dione

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    516-15-4

    11-Ketoprogesterone

  • 640-33-5
    640-33-5

    11α,15α-dihydroxypregn-4-ene-3,20-dione

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