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Gly-Gly - 99%, high purity , CAS No.556-50-3

11 Citations COA COA
    Grade & Purity:
  • ≥99%
In stock
Item Number
G105429
Grouped product items
SKU Size
Availability
 Price Qty
G105429-5g
5g
9
$12.90
G105429-10g
10g
1
$19.90
G105429-25g
25g
7
$39.90
G105429-100g
100g
9
$112.90
G105429-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$385.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Biological Buffers (16) Endogenous Metabolite (959) Metabolic Enzyme/Protease (4860) Metabolite (5307) polypeptide (96)

Basic Description

Synonyms CCG-231053 | Gly-Gly, >=99% (titration) | Glycylglycine, DL- | Glycylglyine | 33903968-DDB2-47F2-9B6C-7C232D1962DA | G-6001 | Glycine dipeptide | Gly-Gly, Vetec(TM) reagent grade, 99% | STL194277 | Gly-Gly, BioUltra, >=99.5% (NT) | 10525P22U0 | H-Gly-Gly
Specifications & Purity ≥99%
Biochemical and Physiological Mechanisms Gly Gly or diglycine peptide is the simplest dipeptide. It may have proteolytic properties. Gly gly is hydrolyzed by diglycidyl dipeptidase.
Storage Temp Room temperature
Shipped In Normal
Product Description

useful pH range 7.5 - 8.9 pKa (25 °C) 8.2

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Peptides
Direct Parent Dipeptides
Alternative Parents N-acyl-alpha amino acids  Alpha amino acid amides  Secondary carboxylic acid amides  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Alpha-dipeptide - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Amino acid or derivatives - Carboxamide group - Amino acid - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Amine - Organic oxygen compound - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
External Descriptors dipeptide

Associated Targets(Human)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC15A1 Tchem Oligopeptide transporter small intestine isoform (922 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC15A2 Tchem Solute carrier family 15 member 2 (186 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Slc15a2 Oligopeptide transporter, kidney isoform (114 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Slc15a1 Solute carrier family 15 member 1 (124 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GAP1 General amino-acid permease GAP1 (481 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488181277
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181277
IUPAC Name 2-[(2-aminoacetyl)amino]acetic acid
INCHI InChI=1S/C4H8N2O3/c5-1-3(7)6-2-4(8)9/h1-2,5H2,(H,6,7)(H,8,9)
InChIKey YMAWOPBAYDPSLA-UHFFFAOYSA-N
Smiles C(C(=O)NCC(=O)O)N
Isomeric SMILES C(C(=O)NCC(=O)O)N
WGK Germany 3
Molecular Weight 132.12
Beilstein 1765223
Reaxy-Rn 1765223
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1765223&ln=

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.

34 results found

Lot Number Certificate Type Date Item
K2426607 Certificate of Analysis Nov 18, 2024 G105429
K2426614 Certificate of Analysis Nov 18, 2024 G105429
K2426612 Certificate of Analysis Nov 18, 2024 G105429
K2426613 Certificate of Analysis Nov 18, 2024 G105429
I2423289 Certificate of Analysis Sep 13, 2024 G105429
I2423287 Certificate of Analysis Sep 13, 2024 G105429
I2423288 Certificate of Analysis Sep 13, 2024 G105429
I2423290 Certificate of Analysis Sep 13, 2024 G105429
I2423286 Certificate of Analysis Sep 13, 2024 G105429
I2403434 Certificate of Analysis Jul 08, 2024 G105429
E2413288 Certificate of Analysis Apr 28, 2024 G105429
E2413289 Certificate of Analysis Apr 28, 2024 G105429
E2413308 Certificate of Analysis Apr 28, 2024 G105429
E2413286 Certificate of Analysis Apr 28, 2024 G105429
E2413287 Certificate of Analysis Apr 28, 2024 G105429
E2413307 Certificate of Analysis Apr 28, 2024 G105429
D2424218 Certificate of Analysis Apr 26, 2024 G105429
D2424219 Certificate of Analysis Apr 26, 2024 G105429
D2424220 Certificate of Analysis Apr 26, 2024 G105429
E2431208 Certificate of Analysis Mar 15, 2024 G105429
E2431212 Certificate of Analysis Mar 15, 2024 G105429
H2323078 Certificate of Analysis Aug 30, 2023 G105429
A2330827 Certificate of Analysis Feb 02, 2023 G105429
A2330828 Certificate of Analysis Feb 02, 2023 G105429
A2330829 Certificate of Analysis Feb 02, 2023 G105429
A2330831 Certificate of Analysis Feb 02, 2023 G105429
D2313757 Certificate of Analysis Feb 02, 2023 G105429
D2313756 Certificate of Analysis Feb 02, 2023 G105429
D2313755 Certificate of Analysis Feb 02, 2023 G105429
H2203367 Certificate of Analysis Sep 19, 2021 G105429
H2203388 Certificate of Analysis Sep 19, 2021 G105429
H2203379 Certificate of Analysis Sep 19, 2021 G105429
H2203387 Certificate of Analysis Sep 19, 2021 G105429
I2114204 Certificate of Analysis Sep 19, 2021 G105429

Show more⌵

Chemical and Physical Properties

Solubility Easily soluble in water, slightly soluble in ethanol, insoluble in ether.
Melt Point(°C) 260-262°C
Molecular Weight 132.120 g/mol
XLogP3 -2.900
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 3
Exact Mass 132.053 Da
Monoisotopic Mass 132.053 Da
Topological Polar Surface Area 92.400 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 123.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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Documents & Articles

Buffer Reference Center
Categories: Technical articles
Tags:
Buffer

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Yuan Yuni, liu Wei, Liu Qi, He Qing, Hu Yuyang, Jiang Xinyu, Chen Xiaoqing.  (2022)  A dual-channel probe based on copper ion-mediated metal organic framework composite for colorimetric and ratiometric fluorescence monitoring of glyphosate degradation in soil and water.  MICROCHIMICA ACTA,  189  (10): (1-10). 
2. Ning Zhang, Zhicheng Pan, Chao Li, Juan Wang, Yao Jin, Shaofeng Song, Mingwang Pan, Jinfeng Yuan.  (2022)  Dipeptide end-capping resultant multiple hydrogen bonds triggering self-healing waterborne polyurethane elastomers.  POLYMER,  246  (124778). 
3. Zijian Zhao, Hui Jiang, Lang Wu, Ning Yu, Zhengwei Luo, Wenhua Geng.  (2022)  Preparation of Magnetic Surface Ion-Imprinted Polymer Based on Functionalized Fe3O4 for Fast and Selective Adsorption of Cobalt Ions from Water.  Water,  14  (2): (261). 
4. Pei Zhu, Yan Wang, Minghang Zhang, Yingdong Wu, Wangfeng Cai.  (2022)  Anions influence on the electrochemical performance of Co3X4 (X = O, Se) for supercapacitor: Experiments and theoretical calculations.  APPLIED SURFACE SCIENCE,  574  (151646). 
5. Zelong Li, Runtao Zhu, Yongqi Liu, Jiaqi Li, Haofeng Gao, Nan Hu.  (2020)  γ-Glutamyltranspeptidase from Bacillus amyloliquefaciens: transpeptidation activity enhancement and L-theanine production.  ENZYME AND MICROBIAL TECHNOLOGY,  140  (109644). 
6. Lijuan Huang, Xin Zhang, Zhuoyong Zhang.  (2019)  UV–vis sensor array combining with chemometric methods for quantitative analysis of binary dipeptide mixture (Gly-Gly/Ala-Gln).  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  221  (117205). 
7. Yajie Wang, Pengyao Xing, Wei An, Mingfang Ma, Minmin Yang, Tianxiang Luan, Ruipeng Tang, Bo Wang, Aiyou Hao.  (2018)  pH-Responsive Dipeptide-Based Dynamic Covalent Chemistry Systems Whose Products and Self-Assemblies Depend on the Structure of Isomeric Aromatic Dialdehydes.  LANGMUIR,  34  (45): (13725–13734). 
8. Yong-Yu Qi, Qian Gan, Ya-Xian Liu, Ya-Hong Xiong, Zong-Wan Mao, Xue-Yi Le.  (2018)  Two new Cu(II) dipeptide complexes based on 5-methyl-2-(2′-pyridyl)benzimidazole as potential antimicrobial and anticancer drugs: Special exploration of their possible anticancer mechanism.  EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,  154  (220). 
9. Chusheng Liu, Haibin Li, Qiqin Wang, Jacques Crommen, Haibo Zhou, Zhengjin Jiang.  (2017)  Preparation and evaluation of 400 μm I.D. polymer-based hydrophilic interaction chromatography monolithic columns with high column efficiency.  JOURNAL OF CHROMATOGRAPHY A,  1509  (83). 
10. Bozhong Cao, Chunyan Xu, Bingchun Jiang, Biao Jin, Jincheng Zhang, Lei Ling, Yusheng Lu, Tianyu Zou, Tong Zhang.  (2024)  Electrolyte Optimization Strategy: Enabling Stable and Eco-Friendly Zinc Adaptive Interfacial Layer in Zinc Ion Batteries.  MOLECULES,  29  (4): (874). 
11. Wei Wei, Fengjian Chu, Guanru Chen, Shiwen Zhou, Cuirong Sun, Hongru Feng, Yuanjiang Pan.  (2024)  Prebiotic Formation of Peptides Through Bubbling and Arc Plasma.  CHEMISTRY-A EUROPEAN JOURNAL,    (e202401809). 

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