Ac-Ala-OH - ≥98% , CAS No.97-69-8

CAS: 97-69-8 Cat. No.: A105813 Peso molecular: 131.13 Número EC: 202-602-0
Disponible para pedir
GRADE & PURITY ≥98%
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 |
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
A105813-5g
5
9,90US$
10g
A105813-10g
2
10,90US$
25g
A105813-25g
4

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
100g
A105813-100g
5

41,90US$

62,90US$
Guardar 21,00 US$ (33.39%)
500g
A105813-500g
1

208,90US$

313,90US$
Guardar 105,00 US$ (33.45%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
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 |
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488186470
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488186470
Sonrisas canónicasCC(C(=O)O)NC(=O)C
IUPAC Name(2S)-2-acetamidopropanoic acid
InChIKeyKTHDTJVBEPMMGL-VKHMYHEASA-N
INCHI1S/C5H9NO3/c1-3(5(8)9)6-4(2)7/h3H,1-2H3,(H,6,7)(H,8,9)/t3-/m0/s1
Isómeros SMILES C[C@@H](C(=O)O)NC(=O)C
WGK Alemania 3
Peso molecular 131.13
Reaxy-Rn 774333
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774333&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
ClaseCarboxylic acids and derivatives
SubclassAmino 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 ParentN-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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

10 results found

Lot NumberCertificate TypeFechaArticulo
I2207222Certificate of AnalysisJun 11, 2026 A105813
I2207223Certificate of AnalysisJun 11, 2026 A105813
I2207224Certificate of AnalysisJun 11, 2026 A105813
I2207240Certificate of AnalysisJun 11, 2026 A105813
B2324095Certificate of AnalysisJul 15, 2022 A105813
B2324098Certificate of AnalysisJul 15, 2022 A105813
B2324126Certificate of AnalysisJul 15, 2022 A105813
I2315112Certificate of AnalysisJul 15, 2022 A105813
J2522091Certificate of AnalysisJul 15, 2022 A105813
B2225480Certificate of AnalysisMar 15, 2022 A105813
Propiedades químicas y físicas
Punto de fusión (°C)122-128°C
Peso molecular131.130 g/mol
XLogP3-0.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass131.058 Da
Monoisotopic Mass131.058 Da
Topological Polar Surface Area66.400 Ų
Heavy Atom Count9
Formal Charge0
Complexity132.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
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,      [PMID:] [10.1016/j.wear.2024.205247]
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,      [PMID:] [10.1016/j.lwt.2024.116217]
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,      [PMID:39256562] [10.1038/s44318-024-00222-1]
Calculadoras de soluciones
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