DL-Propargylglycine - ≥98% , CAS No.64165-64-6

CAS: 64165-64-6 Cat. No.: D133969 Molecular Weight: 113.11 EC Number: 628-118-3
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
PAG | 2WA8F50C3F | 4-PENTYNOIC ACID, 2-AMINO-, (+/-)- | FT-0698061 | Ftc, dl- | H-Propargyl-DL-Gly-OH;(RS)-2-Amino-4-pentynoic acid | 2-amino-4-pentynoic acid, monohydrochloride | AB89124 | 2-Propynylglycine | Propargyl glycine | FU67PLJ48R | AS-18031 | D
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
D133969-250mg
3
$59.90
1g
D133969-1g
3
$171.90
5g
D133969-5g
1

$571.90

$685.90
Save $114.00 (16.62%)
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
PAG | 2WA8F50C3F | 4-PENTYNOIC ACID, 2-AMINO-, (+/-)- | FT-0698061 | Ftc, dl- | H-Propargyl-DL-Gly-OH;(RS)-2-Amino-4-pentynoic acid | 2-amino-4-pentynoic acid, monohydrochloride | AB89124 | 2-Propynylglycine | Propargyl glycine | FU67PLJ48R | AS-18031 | D
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
DL-Propargylglycine (PAG) is an irreversible inhibitor of the enzyme cystathionine γ-lyase (GCL), a key enzyme involved in glutathione synthesis and the metabolic transsulfuration pathway which regulates homocysteine concentration and mediates cysteine sy
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid488186922
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488186922
Canonical SmilesC#CCC(C(=O)O)N
IUPAC Name2-aminopent-4-ynoic acid
InChIKeyDGYHPLMPMRKMPD-UHFFFAOYSA-N
INCHI1S/C5H7NO2/c1-2-3-4(6)5(7)8/h1,4H,3,6H2,(H,7,8)
Isomeric SMILES C#CCC(C(=O)O)N
WGK Germany 3
Molecular Weight 113.11
Reaxy-Rn 1748643
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1748643&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlpha amino acids
Alternative Parents Unsaturated fatty acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Acetylides  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha-amino acid - Unsaturated fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Acetylide - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeDateItem
F2305195Certificate of AnalysisMar 03, 2025 D133969
F2305196Certificate of AnalysisMar 03, 2025 D133969
F2305199Certificate of AnalysisMar 03, 2025 D133969
F2305200Certificate of AnalysisMar 03, 2025 D133969
F2305203Certificate of AnalysisMar 03, 2025 D133969
K2112424Certificate of AnalysisAug 04, 2023 D133969
K2112399Certificate of AnalysisAug 04, 2023 D133969
F2305192Certificate of AnalysisMay 13, 2023 D133969
B2314423Certificate of AnalysisFeb 20, 2023 D133969
L2010024Certificate of AnalysisSep 20, 2022 D133969
L1626011Certificate of AnalysisJan 25, 2022 D133969

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Chemical and Physical Properties
Molecular Weight113.110 g/mol
XLogP3-2.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass113.048 Da
Monoisotopic Mass113.048 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count8
Formal Charge0
Complexity133.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Fu Shaodong, Wang Zhenglei, Han Xiangan, Xu Yuanyuan, Miao Jinfeng.  (2023)  The therapeutic potential for targeting CSE/H2S signaling in macrophages against Escherichia coli infection.  VETERINARY RESEARCH,  54  (1): (1-12).  [PMID:37644526] [10.1186/s13567-023-01203-8]
2. Jia Honglei, Chen Sisi, Liu Dan, Liesche Johannes, Shi Cong, Wang Juan, Ren Meijuan, Wang Xiaofeng, Yang Jun, Shi Wei, Li Jisheng.  (2018)  Ethylene-Induced Hydrogen Sulfide Negatively Regulates Ethylene Biosynthesis by Persulfidation of ACO in Tomato Under Osmotic Stress.  Frontiers in Plant Science,      [PMID:30386366] [10.3389/fpls.2018.01517]
3. Rong-Xin Song, Xiao-Yi Ma, Ting-Ting Zhou, Zhi-Fang Yu, Jun Wang, Bao-Dong Li, Yu-Mo Jing, Han Wang, Yue Fu, Rui-Zhao Lv, Shi-Yan Jia, Xiao-Ming Li, Li-Min Zhang.  (2024)  Excessive hydrogen sulfide-induced activation of NMDA receptors in the colon participates in anxiety- and compulsive-like behaviors in a rodent model of hemorrhagic shock and resuscitation.  INTERNATIONAL IMMUNOPHARMACOLOGY,      [PMID:39332088] [10.1016/j.intimp.2024.113255]
4. Wang Jun, Zhang Nan, Liu Hong-Zheng, Wang Jin-Liang, Zhang Yong-Bo, Su Dong-Dong, Zhang Li-Min, Li Bao-Dong, Miao Hui-Tao, Miao Jun.  (2025)  Hydrogen Sulfide (H2S) Generated in the Colon Induces Neuropathic Pain by Activating Spinal NMDA Receptors in a Rodent Model of Chronic Constriction Injury.  NEUROCHEMICAL RESEARCH,  50  (2): (1-13).  [PMID:39883291] [10.1007/s11064-025-04342-w]
5. Ze Deng, Jiajia Cheng, Yaqi Zhang, Yue Zhao, Zimin Wei, Caihong Song.  (2025)  The inhibition of cystathionine gamma-lyase and cystathionine beta-synthase - a strategy to reduce hydrogen sulfide emissions during livestock manure composting.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:40784225] [10.1016/j.jenvman.2025.126890]
Solution Calculators
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