DL-Alanine - ≥99% , CAS No.302-72-7

CAS: 302-72-7 Cat. No.: A100051 Peso molecular: 89.09 Beilstein Registry Number: 1720250 Número EC: 206-126-4
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
AB02601 | DL-2-Aminopropionic acid | FT-0657966 | DL-Alanine, Vetec(TM) reagent grade, 98% | (R)-(-)-2-AMINOPROPIONIC ACID | alanina | Alanine, L-isomer | D(-)-.alpha.-Alanine | DL-2-Aminopropanoic acid | L-Isomer alanine | (.+/-.)-Alanine | (+/-)-2-AMINO
Storage
Desiccated,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
A100051-25g
1
14,90US$
100g
A100051-100g
2
19,90US$
500g
A100051-500g
1
25,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Desiccated,Room temperature Ships Normal 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.

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Literature proof

Cited in 111 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

DL-Alanine, a racemic mixture of D- and L-alanine, is used as a model reagent for development of amino acid racemic resolution techniques. DL-Alanine is used in mixed ligand (chelate) studies with transition metals such as Cu(II), Zn(ll) and Cd(ll).

Specifications

Sinónimos
AB02601 | DL-2-Aminopropionic acid | FT-0657966 | DL-Alanine, Vetec(TM) reagent grade, 98% | (R)-(-)-2-AMINOPROPIONIC ACID | alanina | Alanine, L-isomer | D(-)-.alpha.-Alanine | DL-2-Aminopropanoic acid | L-Isomer alanine | (.+/-.)-Alanine | (+/-)-2-AMINO
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Desiccated, Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488179535
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179535
Sonrisas canónicasCC(C(=O)O)N
IUPAC Name2-aminopropanoic acid
InChIKeyQNAYBMKLOCPYGJ-UHFFFAOYSA-N
INCHI1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)
Isómeros SMILES CC(C(=O)O)N
WGK Alemania 1
RTECS AY2980000
Peso molecular 89.09
Beilstein 1720250
Reaxy-Rn 635807
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635807&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.

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🔬 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
Direct ParentAlanine and derivatives
Alternative Parents Alpha amino acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alanine or derivatives - Alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alanine and derivatives. These are compounds containing alanine or a derivative thereof resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors alpha-amino acid
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus fumigatus (16427 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida parapsilosis (8521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sporothrix schenckii (1580 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton mentagrophytes (4846 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

39 results found

Lot NumberCertificate TypeFechaArticulo
F2612199Certificate of AnalysisJun 01, 2026 A100051
F2612198Certificate of AnalysisJun 01, 2026 A100051
F2612196Certificate of AnalysisJun 01, 2026 A100051
K2404064Certificate of AnalysisJun 19, 2024 A100051
D2508343Certificate of AnalysisJun 19, 2024 A100051
H2518155Certificate of AnalysisJun 19, 2024 A100051
H2527646Certificate of AnalysisJun 19, 2024 A100051
H2527645Certificate of AnalysisJun 19, 2024 A100051
D2508345Certificate of AnalysisJun 19, 2024 A100051
D2508344Certificate of AnalysisJun 19, 2024 A100051
J2418704Certificate of AnalysisJun 19, 2024 A100051
J2418703Certificate of AnalysisJun 19, 2024 A100051
E2520713Certificate of AnalysisJun 19, 2024 A100051
E2520712Certificate of AnalysisJun 19, 2024 A100051
J2522099Certificate of AnalysisJun 19, 2024 A100051
E2516117Certificate of AnalysisJun 19, 2024 A100051
E2516115Certificate of AnalysisJun 18, 2024 A100051
G2425096Certificate of AnalysisMar 25, 2024 A100051
B2311451Certificate of AnalysisJan 16, 2023 A100051
J2418303Certificate of AnalysisJan 16, 2023 A100051
A2408138Certificate of AnalysisJan 16, 2023 A100051
A2508170Certificate of AnalysisJan 16, 2023 A100051
A2508171Certificate of AnalysisJan 16, 2023 A100051
B2311457Certificate of AnalysisJan 16, 2023 A100051
B2311456Certificate of AnalysisJan 16, 2023 A100051
B2311455Certificate of AnalysisJan 16, 2023 A100051
B2311453Certificate of AnalysisJan 16, 2023 A100051
B2311452Certificate of AnalysisJan 16, 2023 A100051
A2219221Certificate of AnalysisDec 27, 2021 A100051
G2208117Certificate of AnalysisDec 27, 2021 A100051
A2219230Certificate of AnalysisDec 27, 2021 A100051
A2219228Certificate of AnalysisDec 27, 2021 A100051
A2219224Certificate of AnalysisDec 27, 2021 A100051
D2603107Certificate of AnalysisMar 08, 2021 A100051
D2603098Certificate of AnalysisMar 08, 2021 A100051
B2103111Certificate of AnalysisMar 08, 2021 A100051
B2103112Certificate of AnalysisMar 08, 2021 A100051
B2103113Certificate of AnalysisMar 08, 2021 A100051
B2103114Certificate of AnalysisMar 08, 2021 A100051

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Propiedades químicas y físicas
SolubilidadSoluble in water. Slightly soluble in alcohol
Punto de fusión (°C)289 °C (dec.) (lit.)
Peso molecular89.090 g/mol
XLogP3-3.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass89.0477 Da
Monoisotopic Mass89.0477 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity61.800
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
Referencias
1. Shen Zhang, Jinjia Bao, Ling Lv, Yongjie Bai, Yiming Zhang, Yaofang Zhang.  (2023)  Yellow-emitting carbon dots as fluorescent sensors for the rapid determination of curcumin.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38157744] [10.1016/j.saa.2023.123819]
2. Cheng Shen, Yachao Li, Zenan Zeng, Yiming Liu, Yini Xu, Kefurong Deng, Beiling Guo, Dongzhe Zou, Liguo Liu, Xiaoyu Liang, Xianghui Xu.  (2023)  Systemic Administration with Bacteria-Inspired Nanosystems for Targeted Oncolytic Therapy and Antitumor Immunomodulation.  ACS Nano,      [PMID:38064380] [10.1021/acsnano.3c10302]
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4. Yang Yang, Ru Zhao, Hongfei Gao, Zehao Wang, Xinyu Yang, Ming Ruan, Huiyan Gu, Lei Yang, Hao Tian, Changwen Fan, Tingting Liu.  (2023)  β-Cyclodextrin as a booster for ultrasound-assisted extraction of secoiridoids from Gentiana rigescens using a biobased deep eutectic solvent.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2023.117410]
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8. Shizhuang Weng, Le Tang, Mengqing Qiu, Jinghong Wang, Yehang Wu, Rui Zhu, Cong Wang, Pan Li, Wen Sha, Dong Liang.  (2023)  Surface-enhanced Raman spectroscopy charged probes under inverted superhydrophobic platform for detection of agricultural chemicals residues in rice combined with lightweight deep learning network.  ANALYTICA CHIMICA ACTA,      [PMID:37179059] [10.1016/j.aca.2023.341264]
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10. Ze-Yang Hu, Xu-Yang Chen, Xue Yang, Ting Li, Yu-Shun Yang, Sheng-Jun Wang, Kai Wang, Zhi-Gang Hu.  (2023)  Imaging and detection of sulfite in acute liver injury with a novel quinoxaline-based fluorescent probe.  ANALYTICA CHIMICA ACTA,      [PMID:37147051] [10.1016/j.aca.2023.341177]
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16. Rong Li, Zhigao Sun.  (2023)  Improving C2H3Cl2F hydrate formation for cold storage in the presence of amino acids.  Journal of Energy Storage,      [PMID:] [10.1016/j.est.2022.106505]
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19. Yi Zhang, Qingbo Deng, Chang Tang, Minglu Zhang, Zilong Huang, Zhifeng Cai.  (2022)  Fluorescent folic acid-capped copper nanoclusters for the determination of rifampicin based on inner filter effect.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:36228492] [10.1016/j.saa.2022.121944]
20. Jie Xiang, Junyi Zhang, Shunmei Li, Ruo Yuan, Yun Xiang.  (2022)  Aptamer-based and sensitive label-free colorimetric sensing of phenylalanine via cascaded signal amplifications.  ANALYTICA CHIMICA ACTA,      [PMID:36192064] [10.1016/j.aca.2022.340393]
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