Boc-L-Glutamic acid - ≥98% , CAS No.2419-94-5

CAS: 2419-94-5 Cat. No.: B105466 Molecular Weight: 247.25 Beilstein Registry Number: 2418563 EC Number: 882-608-3

GRADE & PURITY ≥98%

Synonyms

MFCD00037297 | AM81694 | N-Boc-L-Glu | Boc-Glu-OH | Boc-L-glutamic acid | N-(tert-Butoxycarbonyl)-L-glutamic Acid | (S)-2-(TERT-BUTOXYCARBONYLAMINO)PENTANEDIOIC ACID | Boc-L-Glu | DTXSID40369224 | (2S)-2-{[(tert-butoxy)carbonyl]amino}pentanedioic acid | J

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

MFCD00037297 | AM81694 | N-Boc-L-Glu | Boc-Glu-OH | Boc-L-glutamic acid | N-(tert-Butoxycarbonyl)-L-glutamic Acid | (S)-2-(TERT-BUTOXYCARBONYLAMINO)PENTANEDIOIC ACID | Boc-L-Glu | DTXSID40369224 | (2S)-2-{[(tert-butoxy)carbonyl]amino}pentanedioic acid | J

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

• Pubchem Sid: 504760916
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504760916
• Canonical Smiles: CC(C)(C)OC(=O)N[C@@H](CCC(O)=O)C(O)=O
• IUPAC Name: (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanedioic acid
• InChIKey: AQTUACKQXJNHFQ-LURJTMIESA-N
• INCHI: 1S/C10H17NO6/c1-10(2,3)17-9(16)11-6(8(14)15)4-5-7(12)13/h6H,4-5H2,1-3H3,(H,11,16)(H,12,13)(H,14,15)/t6-/m0/s1
• Isomeric SMILES: CC(C)(C)OC(=O)N[C@@H](CCC(=O)O)C(=O)O
• WGK Germany: 3
• Molecular Weight: 247.25
• Beilstein: 2418563
• Reaxy-Rn: 2418563
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2418563&ln=

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: Branched fatty acids Dicarboxylic acids and derivatives Carbamate esters Organic carbonic acids and derivatives Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Glutamic acid or derivatives - Branched fatty acid - Dicarboxylic acid or derivatives - Fatty acid - Fatty acyl - Carbamic acid ester - Carbonic acid derivative - Carboxylic acid - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic oxide - Organopnictogen compound - Aliphatic acyclic 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

Data sources

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

Associated Targets(non-human)

Mus musculus (284745 Activities)

Explore this target

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water
• Specific Rotation[α]: -15 ° (C=1, MeOH)
• Melt Point(°C): 110-112°C
• Molecular Weight: 247.240 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 247.106 Da
• Monoisotopic Mass: 247.106 Da
• Topological Polar Surface Area: 113.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 306.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Gerile Gerile, Tsogzolmaa Ganbold, Yizheng Li, Huricha Baigude.  (2017)  Head group configuration increases the biocompatibility of cationic lipids for nucleic acid delivery.  Journal of Materials Chemistry B,  5  (28): (5597-5607).  [PMID:] [10.1039/C7TB00317J]

2. Xiaolei Zhang, Xiaofei Sun, Lintong Zhou, Le Chang, Yan Zhang, Yingxia Zong, Jingjiang Sun, Qingfu Wang.  (2025)  Preparation of Polyester Microspheres by Passerini Three-Component Dispersion Polymerization in Water.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.5c00071]