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  2. Amino Acid Derivatives
  3. N-(tert-Butoxycarbonyl)-N-methyl-L-threonine

N-(tert-Butoxycarbonyl)-N-methyl-L-threonine is a threonine derivative.

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N-(tert-Butoxycarbonyl)-N-methyl-L-threonine Chemical Structure

N-(tert-Butoxycarbonyl)-N-methyl-L-threonine Chemical Structure

CAS No. : 101759-72-2

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Description

N-(tert-Butoxycarbonyl)-N-methyl-L-threonine is a threonine derivative[1].

In Vitro

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Masse moléculaire

233.26

Formule

C10H19NO5

CAS No.
Livraison

Room temperature in continental US; may vary elsewhere.

Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation
Références
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N-(tert-Butoxycarbonyl)-N-methyl-L-threonine Related Classifications

  • Calculateur de molarité

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Nom du produit:
N-(tert-Butoxycarbonyl)-N-methyl-L-threonine
Cat. No.:
HY-W048839
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