E4CPG - ≥98% , CAS No.170846-89-6

CAS: 170846-89-6 Cat. No.: E345274 Molecular Weight: 223.23
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(RS)-α-Ethyl-4-carboxyphenylglycine | 4-(2-amino-1-hydroxy-1-oxobutan-2-yl)benzoic acid
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1mg
E345274-1mg
3
$39.90
5mg
E345274-5mg
3
$89.90
10mg
E345274-10mg
2
$133.90
25mg
E345274-25mg
2
$289.90
50mg
E345274-50mg
1
$519.90
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 -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

E4CPG is a group I/group II metabotropic glutamate receptor antagonist which is more potent than (RS)-MCPG .

Specifications

Synonyms
(RS)-α-Ethyl-4-carboxyphenylglycine | 4-(2-amino-1-hydroxy-1-oxobutan-2-yl)benzoic acid
Specifications & Purity
≥98%
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
ANTAGONIST
Purity
≥98%
Names and Identifiers
Canonical SmilesCCC(C1=CC=C(C=C1)C(=O)O)(C(=O)O)N
IUPAC Name4-(1-amino-1-carboxypropyl)benzoic acid
InChIKeyAIEFWRHRHFRLFT-UHFFFAOYSA-N
INCHI1S/C11H13NO4/c1-2-11(12,10(15)16)8-5-3-7(4-6-8)9(13)14/h3-6H,2,12H2,1H3,(H,13,14)(H,15,16)
Isomeric SMILES CCC(C1=CC=C(C=C1)C(=O)O)(C(=O)O)N
Molecular Weight 223.23
Reaxy-Rn 8414574
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8414574&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 ParentAlpha amino acids
Alternative Parents Phenylpropanes  Benzoic acids  Benzoyl derivatives  Aralkylamines  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Alpha-amino acid - Benzoic acid or derivatives - Benzoic acid - Phenylpropane - Benzoyl - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Primary amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

10 results found

Lot NumberCertificate TypeDateItem
H2416558Certificate of AnalysisMay 06, 2024 E345274
H2416559Certificate of AnalysisMay 06, 2024 E345274
H2416560Certificate of AnalysisMay 06, 2024 E345274
H2416561Certificate of AnalysisMay 06, 2024 E345274
H2416562Certificate of AnalysisMay 06, 2024 E345274
H2416569Certificate of AnalysisMay 06, 2024 E345274
H2416570Certificate of AnalysisMay 06, 2024 E345274
H2416571Certificate of AnalysisMay 06, 2024 E345274
H2416572Certificate of AnalysisMay 06, 2024 E345274
H2416573Certificate of AnalysisMay 06, 2024 E345274
Chemical and Physical Properties
SolubilitySoluble to 100 mM in 1.1 eq. NaOH
Molecular Weight223.220 g/mol
XLogP3-1.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass223.084 Da
Monoisotopic Mass223.084 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count16
Formal Charge0
Complexity284.000
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
Solution Calculators
Reviews

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