Fmoc-Ala-OMe

97%

Reagent Code: #38055
fingerprint
CAS Number 146346-88-5

science Other reagents with same CAS 146346-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.36 g/mol
Formula C₁₉H₁₉NO₄
badge Registry Numbers
MDL Number MFCD20264827
thermostat Physical Properties
Boiling Point 497.3±28.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Fmoc-Ala-OMe is widely used in peptide synthesis as a building block for constructing peptides. It serves as a protected form of alanine, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the methyl ester protects the carboxyl group. This protection allows for selective deprotection and coupling during solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptide chains. It is particularly valuable in the production of custom peptides for research in biochemistry, pharmaceuticals, and drug development. Its stability and ease of handling make it a preferred choice in laboratories focused on peptide chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,188.00
inventory 5g
10-20 days ฿3,735.00
inventory 250mg
10-20 days ฿486.00
inventory 10g
10-20 days ฿6,237.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Fmoc-Ala-OMe
No image available

Fmoc-Ala-OMe is widely used in peptide synthesis as a building block for constructing peptides. It serves as a protected form of alanine, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the methyl ester protects the carboxyl group. This protection allows for selective deprotection and coupling during solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptide chains. It is particularly valuable in the production of custom peptides for research in bioche

Fmoc-Ala-OMe is widely used in peptide synthesis as a building block for constructing peptides. It serves as a protected form of alanine, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the methyl ester protects the carboxyl group. This protection allows for selective deprotection and coupling during solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptide chains. It is particularly valuable in the production of custom peptides for research in biochemistry, pharmaceuticals, and drug development. Its stability and ease of handling make it a preferred choice in laboratories focused on peptide chemistry.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...