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Quality Factory Hot Selling 1,3,5[10]-ESTRATRIENE-3,17BETA-DIOL 3-SULFATE SODIUM SALT 4999-79-5 with Fast Shipping

  • Molecular Formula: C18H24 O5 S . Na
  • Molecular Weight: 374.433
  • Melting Point: 207 °C 
  • Boiling Point: °Cat760mmHg 
  • Flash Point: °C 
  • PSA: 95.04000 
  • Density: g/cm3 
  • LogP: 3.82340 

1,3,5[10]-ESTRATRIENE-3,17BETA-DIOL 3-SULFATE SODIUM SALT(Cas 4999-79-5) Usage

Biochem/physiol Actions

β-Estradiol is a steroid hormone involved in a number of organ functions. It is significantly associated with brain functions including neuroprotection, neurogenesis and synaptic plasticity. β-Estradiol maintains bone homeostasis, hence it is preferred for osteoporosis therapy. 17-β-Estradiol is the most active estrogen generated in our body. During postmenopausal, 17-β-estradiol inhibits oxidative modification in low density lipoprotein. This indicates that estrogen replacement therapy might be useful in treating cardiovascular disease.

General Description

β-Estradiol is secreted by developing ovaries and is predominant during premenopause in women.

InChI:InChI=1/C18H24O5S.Na/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19;/h3,5,10,14-17,19H,2,4,6-9H2,1H3,(H,20,21,22);/q;+1/p-1/t14-,15-,16+,17+,18+;/m1./s1

4999-79-5 Relevant articles

Sulfation of various alcoholic groups by an arylsulfate sulfotransferase from desulfitobacterium hafniense and synthesis of estradiol sulfate

Van Der Horst, Michael A.,Van Lieshout, Johan F. T.,Bury, Aleksandra,Hartog, Aloysius F.,Wever, Ron

supporting information, p. 3501 - 3508 (2013/02/22)

Bacterial arylsulfate sulfotransferases ...

Preparation of trifluoroethyl- and phenyl-protected sulfates using sulfuryl imidazolium salts

Desoky, Ahmed Y.,Hendel, Jennifer,Ingram, Laura,Taylor, Scott Douglas

supporting information; experimental part, p. 1281 - 1287 (2011/03/23)

Sulfuryl imidazolium salts (SIS's), a ne...

PROCESS FOR SELECTIVE SULFATION OF AROMATIC HYDROXYL GROUPS

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Page/Page column 15-16, (2008/12/07)

The present invention relates to process...

4999-79-5 Process route

estradiol
50-28-2

estradiol

p-nitrophenyl sulfate
1080-04-2

p-nitrophenyl sulfate

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

(17β)-3-(sulfooxy)estra-1,3,5(10)-trien-17-ol sodium salt
4999-79-5

(17β)-3-(sulfooxy)estra-1,3,5(10)-trien-17-ol sodium salt

Conditions
Conditions Yield
With arylsulfate sulfotransferase from Desulfitobacterium hafniense; In aq. buffer; at 30 ℃; pH=9; regioselective reaction; Green chemistry; Enzymatic reaction;
57%
C<sub>20</sub>H<sub>25</sub>F<sub>3</sub>O<sub>5</sub>S

C20 H25 F3 O5 S

(17β)-3-(sulfooxy)estra-1,3,5(10)-trien-17-ol sodium salt
4999-79-5

(17β)-3-(sulfooxy)estra-1,3,5(10)-trien-17-ol sodium salt

Conditions
Conditions Yield
With sodium azide; In N,N-dimethyl-formamide; at 70 ℃; Inert atmosphere;
94%

4999-79-5 Upstream products

  • 50-28-2
    50-28-2

    estradiol

  • 865-48-5
    865-48-5

    sodium t-butanolate

  • 1080-04-2
    1080-04-2

    p-nitrophenyl sulfate

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