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  3. Amino Acid Derivatives
  4. Boc-β-Ala-ol

Boc-β-Ala-ol  (Synonyms: 3-(Boc-amino)-1-propanol)

Cat. No.: HY-34738
COA Handling Instructions

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Boc-β-Ala-ol (3-(Boc-amino)-1-propanol) is an alanine derivative with a Boc protecting group at the N-terminus, which can be used to synthesize bioactive peptide mimics, such as Nα-Benzoyl-α-azaornithine phenyl ester, which has trypsin inhibitory activity.

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

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Boc-β-Ala-ol Chemical Structure

Boc-β-Ala-ol Chemical Structure

CAS No. : 58885-58-8

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Boc-β-Ala-ol Related Antibodies

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Description

Boc-β-Ala-ol (3-(Boc-amino)-1-propanol) is an alanine derivative with a Boc protecting group at the N-terminus, which can be used to synthesize bioactive peptide mimics, such as Nα-Benzoyl-α-azaornithine phenyl ester, which has trypsin inhibitory activity[1].

Molecular Weight

175.23

Formula

C8H17NO3
CAS No.
Appearance

Liquid

Color

Colorless to light yellow

Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation

Purity: 99.72%

COA (243 KB) HNMR (116 KB) GC (190 KB)

Handling Instructions (2659 KB)
References
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Boc-β-Ala-ol Related Classifications

  • Molarity Calculator

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The molarity calculator equation

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

Mass   Concentration   Volume   Molecular Weight *
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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:

Boc-β-Ala-ol58885-58-83-(Boc-amino)-1-propanolAmino Acid DerivativesProtecting groupsAlaninePeptide synthesisDerivativesInhibitorinhibitorinhibit

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