Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 57-87-4 Chemical Structure| 57-87-4
Chemical Structure| 57-87-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Ergosterol is a biological precursor of Vitamin D2, found in cell membranes of fungi and protozoa.

Synonyms: Ergosterin; Provitamin D; Ergosta-5,7,22-trien-3beta-ol

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Ergosterol

CAS No. :57-87-4
Formula : C28H44O
M.W : 396.65
SMILES Code : O[C@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H]([C@H](C)/C=C/[C@@H](C(C)C)C)CC[C@@]4([H])C3=CC=C2C1
Synonyms :
Ergosterin; Provitamin D; Ergosta-5,7,22-trien-3beta-ol
English Name :(3S,9S,10R,13R,14R,17R)-17-((2R,5R,E)-5,6-Dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
MDL No. :MFCD00003623
InChI Key :DNVPQKQSNYMLRS-APGDWVJJSA-N
Pubchem ID :444679

Safety of Ergosterol

Application In Synthesis of Ergosterol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 57-87-4 ]

[ 57-87-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 57-87-4 ]
  • [ 474-69-1 ]
YieldReaction ConditionsOperation in experiment
29% With 9-acetylanthracene In tetrahydrofuran at 10 - 15℃; for 8.33333h; UV-irradiation; 1; 2; 11; 12 Example 11 Mix 1g of ergosterol, 0.005g of 9-acetylanthracene and 20mL of tetrahydrofuran to obtain solution A; at 10-15 , use solution DL-UVB-UV315-40W LED ultraviolet lamp to irradiate solution A, and the illumination time is 500min. Solution B was obtained after the illumination was completed; the solvent was distilled off under reduced pressure on the solution B, and 0.29 g of photosterol L2 was obtained by column separation. In this example, the yield of photosterol L2 was 29%.
With ethanol; benzene Irradiation.UV-Licht (λ: > 280 mμ); Isolierung aus der erhaltenen Verbindung mit Ergocalciferol ueber das <i>O</i>-Acetyl-Derivat oder das <i>O</i>-<3.5-Dinitro-benzoyl>-Derivat;
In ethanol Irradiation;
 

Historical Records

Categories