H-Sar-OtBu.HCl

97%

Reagent Code: #105820
label
Alias Sarcosine tert-butyl hydrochloride;N-Methylglycine tert-butyl hydrochloride
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CAS Number 5616-81-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.66 g/mol
Formula C₇H₁₅NO₂HCl
badge Registry Numbers
MDL Number MFCD00080936
thermostat Physical Properties
Melting Point 137-141 °C (dec.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily used in peptide synthesis as a protecting group for amino acids. The tert-butyloxycarbonyl (OtBu) group helps to shield reactive sites during the synthesis process, ensuring selective reactions and preventing unwanted side reactions. It is particularly useful in solid-phase peptide synthesis (SPPS), where it protects the amino group of sarcosine (Sar), allowing for the stepwise construction of peptides. After the synthesis is complete, the OtBu group can be easily removed under mild acidic conditions, making it a convenient choice for peptide chemists. Its application is crucial in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology.

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Test Parameter Specification
Carbon (By Elemental Analysis) 44.6-47.9
Nitrogen 7.4-8
Purity (HPLC) 97-100%
Appearance White To Off-White Powder
Infrared Spectrum Conforms To Structure
Solubility Clear, colorless to light yellow, 25 mg/mL H2O

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days $71.58
inventory 5g
10-20 days $241.79
inventory 25g
10-20 days $987.31
H-Sar-OtBu.HCl
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The tert-butyloxycarbonyl (OtBu) group helps to shield reactive sites during the synthesis process, ensuring selective reactions and preventing unwanted side reactions. It is particularly useful in solid-phase peptide synthesis (SPPS), where it protects the amino group of sarcosine (Sar), allowing for the stepwise construction of peptides. After the synthesis is complete, the OtBu group can be easily removed under mild acidic conditions, making it a convenient choice for peptide chemists. Its application is crucial in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology.
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