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Glycine Anhydride - >98.0%(N), high purity , CAS No.106-57-0

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Glycine Anhydride - >98.0%(N), high purity , CAS No.106-57-0

1 Citations

COA

Grade & Purity:

≥98%(N)

Cas Number: 106-57-0
Molecular Weight: 114.1
Beilstein Registry Number: 24264
MDL number: MFCD00006009
PubChem CID: 7817
PubChem SID: 488180576

In stock

Item Number

G156851

Grouped product items
SKU	Size	Availability	Price
G156851-5g	5g	1	$9.90
G156851-25g	25g	7	$38.90
G156851-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$136.90
G156851-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$615.90

View related series

Piperazines (158) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms	Glycine, cyclic peptide \| InChI=1/C4H6N2O2/c7-3-1-5-4(8)2-6-3/h1-2H2,(H,5,8)(H,6,7 \| 2,5-PIPERAZINEDIONE [MI] \| G0100 \| Glycylglycine lactam \| Piperazinedione \| 2,5-Diazacyclohexane-1,4-dione \| CYCLO-GLYCYLGLYCINE (3,3,6,6-D4) \| TETRAHYDRO-2,5-PYRAZINEDIO
Specifications & Purity	≥98%(N)
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives
Direct Parent	Alpha amino acids and derivatives
Alternative Parents	2,5-dioxopiperazines Secondary carboxylic acid amides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Alpha-amino acid or derivatives - Dioxopiperazine - 2,5-dioxopiperazine - 1,4-diazinane - Piperazine - Secondary carboxylic acid amide - Lactam - Carboxamide group - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pseudomonas aeruginosa (123386 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

lasR Transcriptional activator protein lasR (432 Activities)

Discover Target: lasR

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	488180576
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180576
IUPAC Name	piperazine-2,5-dione
INCHI	InChI=1S/C4H6N2O2/c7-3-1-5-4(8)2-6-3/h1-2H2,(H,5,8)(H,6,7)
InChIKey	BXRNXXXXHLBUKK-UHFFFAOYSA-N
Smiles	C1C(=O)NCC(=O)N1
Isomeric SMILES	C1C(=O)NCC(=O)N1
RTECS	TL6325250
Molecular Weight	114.1
Beilstein	24264
Reaxy-Rn	112112
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=112112&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.

15 results found

Lot Number	Certificate Type	Date	Item
I2425382	Certificate of Analysis	Oct 08, 2024	G156851
I2425383	Certificate of Analysis	Oct 08, 2024	G156851
I2425384	Certificate of Analysis	Oct 08, 2024	G156851
F2017057	Certificate of Analysis	Apr 03, 2024	G156851
L2208097	Certificate of Analysis	Aug 20, 2022	G156851
K2214569	Certificate of Analysis	Aug 17, 2022	G156851
D2314098	Certificate of Analysis	Aug 17, 2022	G156851
K2214570	Certificate of Analysis	Aug 17, 2022	G156851
K2214520	Certificate of Analysis	Aug 17, 2022	G156851
F2217169	Certificate of Analysis	Jun 24, 2022	G156851
H2420034	Certificate of Analysis	Jun 24, 2022	G156851
F2217059	Certificate of Analysis	Jun 24, 2022	G156851
F2217061	Certificate of Analysis	Jun 24, 2022	G156851
F2217064	Certificate of Analysis	Jun 24, 2022	G156851
I2406188	Certificate of Analysis	Jun 24, 2022	G156851

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Chemical and Physical Properties

Solubility	Soluble in water (142mg/L).
Molecular Weight	114.100 g/mol
XLogP3	-1.300
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	114.043 Da
Monoisotopic Mass	114.043 Da
Topological Polar Surface Area	58.200 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	116.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Ji Liu, Wei Zhao, Shuang-wei Yang, Bin Hu, Ming-xin Xu, Shan-Wei Ma, Qiang Lu. (2021) Formation mechanism of NOx precursors during the pyrolysis of 2,5-diketopiperazine based on experimental and theoretical study. SCIENCE OF THE TOTAL ENVIRONMENT, 801 (149663).

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