N-Propargylglycine

Name: N-Propargylglycine
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 58160-95-5
Cat. No. CS-0343178
Purity≥95%
MDL No.MFCD11168312

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Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

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General Information

CAS No. 58160-95-5
Cat. No. CS-0343178
Purity ≥95%
MDL No. MFCD11168312
Storage Store at room temperature, keep dry and cool
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₅H₇NO₂
Molecular Weight 113.11
Synonym(s) None
SMILES O=C(O)CNCC#C

Description

N-Propargylglycine features a terminal alkyne group poised for efficient bioorthogonal conjugation, enabling site-specific labeling in complex biological systems. This bench-stable amino acid derivative integrates seamlessly into peptide synthesis workflows and serves as a key building block for probing protein function through click chemistry applications.

Application

N-Propargylglycine serves as a versatile building block in synthetic organic chemistry, enabling efficient access to bioactive heterocycles and peptidomimetics. Its propargyl group facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the α-amino acid backbone supports standard peptide coupling protocols. The compound exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, making it ideal for modular library synthesis and medicinal chemistry campaigns requiring click chemistry-enabled scaffolds.

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

Quality Control

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Computational Chemistry Data

TPSA 49.33
LogP -0.7062
H_Acceptors 2
H_Donors 2
Rotatable_Bonds 3

Other Classifications

Life Science Amino Acids and their Derivatives

Life Science Click Chemistry Reagents Alkyne

Building Blocks Skeleton Fatty chain compounds

Building Blocks Functional Group Alkyne

Chemical Biology Conjugation Chemistry/Click Chemistry Terminal Alkynes

Chemical Biology Peptide Chemistry Amino Acid Derivatives

Chemical Biology Pharmaceutical Development and Drug Discovery Research Conjugation Chemistry/Click Chemistry Terminal Alkynes

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N-Propargylglycine

CAS No. 58160-95-5

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