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Ac-Ala-OH - 98%, high purity , CAS No.97-69-8

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Ac-Ala-OH - 98%, high purity , CAS No.97-69-8

3 Citations

COA

Grade & Purity:

≥98%

Cas Number: 97-69-8
Molecular Weight: 131.13
EC Number: 202-602-0
MDL number: MFCD00063132
PubChem CID: 88064
PubChem SID: 488186470

In stock

Item Number

A105813

Grouped product items
SKU	Size	Availability	Price
A105813-5g	5g	5	$60.90
A105813-10g	10g	2	$108.90
A105813-25g	25g	4	$243.90
A105813-100g	100g	5	$876.90
A105813-500g	500g	1	$3,945.90

View related series

Metabolite (5307)

Basic Description

Synonyms	N-ACETYLALANINE \| s3094 \| 4/'-Chloro-2,2/':6/',2/'/'-terpyridine \| EINECS 202-602-0 \| n-acetyl alanine \| N-Acetyl-L-alanine \| N-Acetylsuperoxide dismutase (human clone pS 61-10 copper-zinc subunit protein moiety reduced) \| AKOS010366966 \| DTXSID50861704 \|
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

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
        Level7 N-acyl-alpha amino acids and derivatives
        Level8 N-acyl-alpha amino acids
        Level9 N-acyl-L-alpha-amino acids

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 - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives - N-acyl-alpha amino acids
Direct Parent	N-acyl-L-alpha-amino acids
Alternative Parents	Alanine and derivatives Acetamides Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	N-acyl-l-alpha-amino acid - Alanine or derivatives - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors	L-alanine derivative - N-acetyl-L-amino acid
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

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	488186470
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488186470
IUPAC Name	(2S)-2-acetamidopropanoic acid
INCHI	InChI=1S/C5H9NO3/c1-3(5(8)9)6-4(2)7/h3H,1-2H3,(H,6,7)(H,8,9)/t3-/m0/s1
InChIKey	KTHDTJVBEPMMGL-VKHMYHEASA-N
Smiles	CC(C(=O)O)NC(=O)C
Isomeric SMILES	C[C@@H](C(=O)O)NC(=O)C
WGK Germany	3
Molecular Weight	131.13
Reaxy-Rn	774333
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774333&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.

9 results found

Lot Number	Certificate Type	Date	Item
I2207240	Certificate of Analysis	Jul 15, 2022	A105813
B2324095	Certificate of Analysis	Jul 15, 2022	A105813
I2207222	Certificate of Analysis	Jul 15, 2022	A105813
I2315112	Certificate of Analysis	Jul 15, 2022	A105813
B2324098	Certificate of Analysis	Jul 15, 2022	A105813
B2324126	Certificate of Analysis	Jul 15, 2022	A105813
I2207224	Certificate of Analysis	Jul 15, 2022	A105813
I2207223	Certificate of Analysis	Jul 15, 2022	A105813
B2225480	Certificate of Analysis	Mar 15, 2022	A105813

Chemical and Physical Properties

Melt Point(°C)	122-128°C
Molecular Weight	131.130 g/mol
XLogP3	-0.900
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	131.058 Da
Monoisotopic Mass	131.058 Da
Topological Polar Surface Area	66.400 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	132.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
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. Mingyuan Dou, Qing Feng, Jing Yang, Shuai Zou, Kangchun Li, Zhenpeng Li, Maoli Yang, Fuchuan Huang. (2024) Evaluation of rheological properties and tribological properties of choline/acetylamino acid ionic liquids at different frequencies. WEAR, 540-541 (205247).
2. Yuting Li, Xiaotong Li, Jinshun Ye, Zhenzhao Weng, Xiaozhen Liu, Fengyuan Liu, Jingkun Yan, Lin Li. (2024) Reactivity of amino acid residues towards 4-methylbenzoquinone: Effect on the site-specificity of quinone-protein reaction. LWT-FOOD SCIENCE AND TECHNOLOGY, 200 (116217).
3. SunHongzheng , HanLongsen , GuoYueshuai , AnHuiqing , WangBing , ZhangXiangzheng , LiJiashuo , JiangYingtong , WangYue , SunGuangyi , ZhuShuai , TangShoubin , GeJuan , ChenMinjian , GuoXuejiang , WangQiang. (2024) The global phosphorylation landscape of mouse oocytes during meiotic maturation. EMBO JOURNAL,

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