Phthalyl-DL-glutamic Acid - ≥98% , CAS No.6349-98-0

CAS: 6349-98-0 Cat. No.: P160769 Molecular Weight: 277.23 EC Number: 228-754-8

COA

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Phthalyl-DL-glutamic Acid - ≥98% CAS No(6349-98-0) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY ≥98%

Synonyms

EU-0100956 | MFCD00023059 | Ba 2733 | N-Phtaloylglutamic acid | N-Phthaloyl-DL-glutamic acid | SR-01000075452-1 | N-Phthalyl-dl-glutaminsaure | Tox21_500956 | 42UJ0Z625V | A816489 | N-(alpha-Maleimidoacetoxy)succinimide | 4-Amino-1-methyl-3-propylpyrazole

Storage

Store at 2-8°C

Shipped In

Wet ice

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 Solution Calculators Reviews

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Why this grade

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

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Storage & shipping

Store at 2-8°C Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms

Specifications & Purity

≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

Canonical Smiles	C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O
IUPAC Name	2-(1,3-dioxoisoindol-2-yl)pentanedioic acid
InChIKey	FEFFSKLJNYRHQN-UHFFFAOYSA-N
INCHI	1S/C13H11NO6/c15-10(16)6-5-9(13(19)20)14-11(17)7-3-1-2-4-8(7)12(14)18/h1-4,9H,5-6H2,(H,15,16)(H,19,20)
Isomeric SMILES	C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)O
RTECS	MA3810000
Alternate CAS	2301-52-2
Molecular Weight	277.23
Reaxy-Rn	90137

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 Alpha amino acids and derivatives
        Level7 Glutamic acid 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 - Alpha amino acids and derivatives
Direct Parent	Glutamic acid and derivatives
Alternative Parents	Indolyl carboxylic acids and derivatives Phthalimides Isoindoles Indoles N-substituted carboxylic acid imides Dicarboxylic acids and derivatives Benzenoids Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Glutamic acid or derivatives - Indolyl carboxylic acid derivative - Phthalimide - Isoindolone - Indole - Isoindoline - Isoindole - Isoindole or derivatives - Dicarboxylic acid or derivatives - Carboxylic acid imide, n-substituted - Benzenoid - Carboxylic acid imide - Azacycle - Carboxylic acid - Organoheterocyclic compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description	This 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	Not available
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)

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Item
L2502548	Certificate of Analysis	Oct 10, 2025	P160769
L2502549	Certificate of Analysis	Oct 10, 2025	P160769
L2502550	Certificate of Analysis	Oct 10, 2025	P160769
L2502551	Certificate of Analysis	Oct 10, 2025	P160769

Solubility	Solubility in Methanol almost transparency
Melt Point(°C)	192 °C
Molecular Weight	277.230 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	5
Exact Mass	277.059 Da
Monoisotopic Mass	277.059 Da
Topological Polar Surface Area	112.000 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	436.000
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