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L-Glutamic acid di-tert-butyl ester hydrochloride - 97%, high purity , CAS No.32677-01-3

COA

Grade & Purity:

≥97%

Cas Number: 32677-01-3
Molecular Weight: 295.8
Beilstein Registry Number: 3573738
MDL number: MFCD00058003
PubChem CID: 208636
PubChem SID: 504757837

In stock

Item Number

G116986

Grouped product items
SKU	Size	Availability	Price
G116986-1g	1g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$11.90
G116986-5g	5g	3	$48.90
G116986-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$78.90
G116986-25g	25g	3	$177.90
G116986-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$639.90

View related series

Class A GPCR (4138) GPCR/G Protein (3172) Neurokinin Receptor (49) Neuronal Signaling (3320)

Basic Description

Synonyms	glutamic acid di-t-butyl ester hydrochloride \| H-Glu(OtBu)-OtBu.HCl \| di-tert butyl L-glutamate hydrochloride \| L-Glutamic acid di-tert-butyl ester HCl \| NSC 94681 \| Picosulfato sodico [INN-Spanish] \| SCHEMBL18476 \| Di-tert-butyl (2S)-2-aminopentanedioate
Specifications & Purity	≥97%
Biochemical and Physiological Mechanisms	Glutamic acid di-tert butyl ester (GTBE) possesses convulsant properties in mice and rats. It might have unique pharmacological features that set it apart from other convulsant medications.L-Glutamic acid di-tert-butyl ester is C-terminal and R-chain bloc
Storage Temp	Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Application L-Glutamic acid di-tert-butyl ester may be useful in the synthesis of substance P antagonistic peptides.

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	Alpha amino acid esters Fatty acid esters Dicarboxylic acids and derivatives Carboxylic acid esters Organopnictogen compounds Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Glutamic acid or derivatives - Alpha-amino acid ester - Fatty acid ester - Dicarboxylic acid or derivatives - Fatty acyl - Carboxylic acid ester - Organic nitrogen compound - Hydrochloride - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Amine - 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
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

Names and Identifiers

Pubchem Sid	504757837
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504757837
IUPAC Name	ditert-butyl (2S)-2-aminopentanedioate;hydrochloride
INCHI	InChI=1S/C13H25NO4.ClH/c1-12(2,3)17-10(15)8-7-9(14)11(16)18-13(4,5)6;/h9H,7-8,14H2,1-6H3;1H/t9-;/m0./s1
InChIKey	LFEYMWCCUAOUKZ-FVGYRXGTSA-N
Smiles	CC(C)(C)OC(=O)CCC(C(=O)OC(C)(C)C)N.Cl
Isomeric SMILES	CC(C)(C)OC(=O)CC[C@@H](C(=O)OC(C)(C)C)N.Cl
WGK Germany	3
Molecular Weight	295.8
Beilstein	3573738
Reaxy-Rn	4028099
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4028099&ln=

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.

4 results found

Lot Number	Certificate Type	Date	Item
A2125376	Certificate of Analysis	Dec 13, 2024	G116986
D1725079	Certificate of Analysis	Nov 01, 2024	G116986
I2206801	Certificate of Analysis	Jul 03, 2022	G116986
I2206800	Certificate of Analysis	Jul 03, 2022	G116986

Chemical and Physical Properties

Solubility	Methanol (Slightly), Water (Slightly)
Sensitivity	Air & Heat & Moisture sensitive
Melt Point(°C)	118-124°C
Molecular Weight	295.800 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	8
Exact Mass	295.155 Da
Monoisotopic Mass	295.155 Da
Topological Polar Surface Area	78.600 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	299.000
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	2

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