2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetic acid hydrate

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Reagent Code: #97421
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CAS Number 212651-47-3

science Other reagents with same CAS 212651-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.35 g/mol
Formula C₁₈H₁₉NO₅
thermostat Physical Properties
Boiling Point 512.8°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound, Fmoc-N-methylglycine hydrate (also known as Fmoc-Sar-OH hydrate), serves as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the nitrogen of N-methylglycine (sarcosine), offering stability in basic conditions and easy removal under mild acidic conditions. This prevents unwanted side reactions, facilitating precise peptide chain assembly. Its broad compatibility with solvents and reagents positions it as a vital intermediate for synthesizing complex peptides and proteins in pharmaceutical and biochemical applications. The hydrate form improves stability, solubility, and ease of handling in lab settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿288.00
inventory 25g
10-20 days ฿972.00
inventory 100g
10-20 days ฿3,168.00
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2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetic acid hydrate
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This compound, Fmoc-N-methylglycine hydrate (also known as Fmoc-Sar-OH hydrate), serves as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the nitrogen of N-methylglycine (sarcosine), offering stability in basic conditions and easy removal under mild acidic conditions. This prevents unwanted side reactions, facilitating precise peptide chain assembly. Its broad compatibility with solvents and reagents positions it as a vital interme

This compound, Fmoc-N-methylglycine hydrate (also known as Fmoc-Sar-OH hydrate), serves as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the nitrogen of N-methylglycine (sarcosine), offering stability in basic conditions and easy removal under mild acidic conditions. This prevents unwanted side reactions, facilitating precise peptide chain assembly. Its broad compatibility with solvents and reagents positions it as a vital intermediate for synthesizing complex peptides and proteins in pharmaceutical and biochemical applications. The hydrate form improves stability, solubility, and ease of handling in lab settings.

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