3-Aminobutanoic acid - ≥97% , CAS No.541-48-0

Name: 3-Aminobutanoic acid - ≥97% , CAS No.541-48-0
Brand: Aladdin Scientific
SKU: A100948
Availability: InStock

CAS: 541-48-0 Cat. No.: A100948 Molecular Weight: 103.12 Beilstein Registry Number: 1720563 EC Number: 208-783-2

4 Citations COA

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3-Aminobutanoic acid - ≥97% CAS No(541-48-0) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY ≥97%

Synonyms

Storage

Room temperature

Shipped In

Normal

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Citations of This Product References Solution Calculators Reviews

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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal 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.

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Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

3-Aminobutanoic acid is a biochemical used in proteomics research
A biochemical used in proteomics research

Specifications

Synonyms

Specifications & Purity

≥97%

Storage

Room temperature

Shipped In

Normal

Purity

≥97%

Names and Identifiers

Pubchem Sid	504752033
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752033
Canonical Smiles	CC(CC(=O)O)N
IUPAC Name	3-aminobutanoic acid
InChIKey	OQEBBZSWEGYTPG-UHFFFAOYSA-N
INCHI	1S/C4H9NO2/c1-3(5)2-4(6)7/h3H,2,5H2,1H3,(H,6,7)
Isomeric SMILES	CC(CC(=O)O)N
WGK Germany	3
RTECS	EK7713333
Alternate CAS	167222-96-0
Molecular Weight	103.12
Beilstein	1720563
Reaxy-Rn	1720563
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720563&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

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 Beta 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	Beta amino acids and derivatives
Alternative Parents	Fatty acids and conjugates Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Beta amino acid or derivatives - Fatty acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom.
External Descriptors	monocarboxylic acid - beta-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

3D Structure

Associated Targets(Human)

SLC6A1 Tclin GABA transporter 1 (308 Activities)

Discover Target: SLC6A1

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

SLC6A11 Tchem GABA transporter 3 (176 Activities)

Discover Target: SLC6A11

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

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Item
H2120149	Certificate of Analysis	Jun 09, 2025	A100948
H2120150	Certificate of Analysis	Jun 09, 2025	A100948
H2120151	Certificate of Analysis	Jun 09, 2025	A100948
H2519141	Certificate of Analysis	Jul 01, 2024	A100948
B2302511	Certificate of Analysis	Dec 20, 2022	A100948
B2302586	Certificate of Analysis	Dec 20, 2022	A100948
B2302604	Certificate of Analysis	Dec 20, 2022	A100948
B2302606	Certificate of Analysis	Dec 20, 2022	A100948
I2315119	Certificate of Analysis	Dec 20, 2022	A100948
B2321062	Certificate of Analysis	Apr 15, 2021	A100948

Solubility	Soluble in water
Melt Point(°C)	189°C
Molecular Weight	103.120 g/mol
XLogP3	-3.100
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	103.063 Da
Monoisotopic Mass	103.063 Da
Topological Polar Surface Area	63.300 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	72.100
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1