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  3. Amino Acid Derivatives
  4. Fmoc-(S)-2-(4-pentenyl)Ala-OH

Fmoc-(S)-2-(4-pentenyl)Ala-OH 

Cat. No.: HY-W004864 Purity: 99.92%
COA Handling Instructions

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Fmoc-(S)-2-(4-pentenyl)Ala-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize biologically active secretin analogs.

For research use only. We do not sell to patients.

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Fmoc-(S)-2-(4-pentenyl)Ala-OH Chemical Structure

Fmoc-(S)-2-(4-pentenyl)Ala-OH Chemical Structure

CAS No. : 288617-73-2

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Based on 1 publication(s) in Google Scholar

Fmoc-(S)-2-(4-pentenyl)Ala-OH Related Antibodies

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Description

Fmoc-(S)-2-(4-pentenyl)Ala-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize biologically active secretin analogs[1].

Molecular Weight

379.45

Formula

C23H25NO4
CAS No.
Appearance

Solid

Color

White to light yellow

Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Store at room temperature 3 years

In solvent -80°C 2 years
-20°C 1 year
Purity & Documentation

Purity: 99.92%

COA (250 KB) HNMR (126 KB) RP-HPLC (232 KB) LCMS (97 KB)

Handling Instructions (2659 KB)
References
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Fmoc-(S)-2-(4-pentenyl)Ala-OH Related Classifications

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The molarity calculator equation

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
Help & FAQs
  • Do most proteins show cross-species activity?

    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.

Keywords:

Fmoc-(S)-2-(4-pentenyl)Ala-OH288617-73-2Amino Acid DerivativesProtective groupsamino acidsderivativespreparation and synthesisInhibitorinhibitorinhibit

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