L(+)-Glutamic acid - Animal Free,USP,JP,Ph.Eur.,for cell culture,≥98.5% , CAS No.56-86-0

CAS: 56-86-0 Cat. No.: L774633 Molecular Weight: 147.13 Beilstein Registry Number: 1723801 EC Number: 200-293-7
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GRADE & PURITY Animal Free ? Animal-free — produced without animal-derived components to reduce contamination risk. Use in biomanufacturing and culture avoiding animal-origin material. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance. JP ? Japanese Pharmacopoeia grade — conforms to JP monograph standards. Use for pharmaceutical products subject to Japanese regulatory requirements. Ph.Eur. ? European Pharmacopoeia grade — conforms to Ph.Eur. monographs across EU member states. Use for pharmaceutical work needing European compendial compliance. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥98.5%
Synonyms
DTXCID30659 | glt | 1ii5 | Glutamate, L- | Glutamic acid, (S)- | Glutaton | glutamate | L-Glutaminic acid | Gamma-L-Glutamic Acid | EC 200-293-7 | L-glutamic acid | (2S)-2-aminopentanedioate | (S)-Glutamic acid | L-alpha-Aminoglutaric acid
Storage
Room temperature,Argon charged,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100g
L774633-GMP-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$88.90
500g
L774633-GMP-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$288.90
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Why this grade

Animal Free,USP,JP,Ph.Eur.,for cell culture,≥98.5% Animal Free,for Cell culture,JP,Ph.Eur.,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged,Cool 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 39 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
DTXCID30659 | glt | 1ii5 | Glutamate, L- | Glutamic acid, (S)- | Glutaton | glutamate | L-Glutaminic acid | Gamma-L-Glutamic Acid | EC 200-293-7 | L-glutamic acid | (2S)-2-aminopentanedioate | (S)-Glutamic acid | L-alpha-Aminoglutaric acid
Specifications & Purity
Animal Free, USP, JP, Ph.Eur., for cell culture, ≥98.5%
Storage
Room temperature, Argon charged, Cool
Shipped In
Normal
Grade
Animal Free, for Cell culture, JP, Ph.Eur., USP
Purity
≥98.5%
Names and Identifiers
Canonical SmilesN[C@@H](CCC(O)=O)C(O)=O
IUPAC Name(2S)-2-aminopentanedioic acid
InChIKeyWHUUTDBJXJRKMK-VKHMYHEASA-N
INCHI1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1
Isomeric SMILES C(CC(=O)O)[C@@H](C(=O)O)N
WGK Germany 1
Molecular Weight 147.13
Beilstein 1723801
Reaxy-Rn 1723799
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723799&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
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentGlutamic acid and derivatives
Alternative Parents L-alpha-amino acids  Amino fatty acids  Dicarboxylic acids and derivatives  Amino acids  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Glutamic acid or derivatives - Alpha-amino acid - L-alpha-amino acid - Amino fatty acid - Dicarboxylic acid or derivatives - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as glutamic acid and derivatives. These are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Common amino acids - Amino acids
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SensitivityMoisture sensitive.
Specific Rotation[α]32 ° (C=5, HCl)
Melt Point(°C)205°C
Molecular Weight147.130 g/mol
XLogP3-3.700
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass147.053 Da
Monoisotopic Mass147.053 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity145.000
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
Documents & Articles
GMP
From Spec to Bench: Understanding and Using USP Grade Reagents
JP Grade Reagents Explained
For Cell Culture
List of Natural Amino Acids
Bio-based Chemicals: From Platform Molecules to Application Scenarios — Trend Insights and Aladdin’s Product Portfolio
Structure, Function, and Applications of Glutamate Dehydrogenase
Key Enzymes in Amino Acid Metabolism: A Mechanistic Framework and Research Applications
G Protein–Coupled Receptors (GPCRs): Structure, Signaling, and Drug Targets
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Neurosteroids and Protective Mechanisms in the Central Nervous System
Molecular Basis of Ferroptosis-Immune Metabolism Crosstalk
Methods and Applications for the Determination of Amino Acid Content and Composition
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Citations of This Product
References
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