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α-Amino-γ-butyrolactone Hydrobromide - >98.0%(N)(T), high purity , CAS No.6305-38-0

    Grade & Purity:
  • ≥98%(N)(T)
In stock
Item Number
A151131
Grouped product items
SKU Size
Availability
Price Qty
A151131-200mg
200mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$9.90
A151131-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$32.90
A151131-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$94.90
A151131-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$423.90
A151131-100g
100g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,523.90

Basic Description

Synonyms (+/-)-alpha-Amino-gamma-butyrolactone hydrobromide | 2-aminobutyrolactone hydrobromide | alpha-Aminobutyrolactone hydrobromide | 2-nitro-benzamide | SCHEMBL1034274 | alpha-Amino-gamma-butyrolactone hydrobromide | (+/-)-alpha-Amino-gamma-butyrolactone hydr
Specifications & Purity ≥98%(N)(T)
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

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 Alpha amino acid esters
Alternative Parents Gamma butyrolactones  Tetrahydrofurans  Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Hydrobromides  Carbonyl compounds  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Alpha-amino acid ester - Gamma butyrolactone - Tetrahydrofuran - Carboxylic acid ester - Lactone - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrobromide - Amine - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
External Descriptors Not available

Names and Identifiers

IUPAC Name 3-aminooxolan-2-one;hydrobromide
INCHI InChI=1S/C4H7NO2.BrH/c5-3-1-2-7-4(3)6;/h3H,1-2,5H2;1H
InChIKey MKLNTBLOABOJFZ-UHFFFAOYSA-N
Smiles C1COC(=O)C1N.Br
Isomeric SMILES C1COC(=O)C1N.Br
WGK Germany 3
Molecular Weight 182.02
Beilstein 4530080
Reaxy-Rn 4530084
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4530084&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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Lot Number Certificate Type Date Item
G2417128 Certificate of Analysis Apr 18, 2024 A151131

Chemical and Physical Properties

Solubility Soluble in water; Soluble in Methanol,Ethanol
Melt Point(°C) 237 °C
Molecular Weight 182.020 g/mol
XLogP3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 0
Exact Mass 180.974 Da
Monoisotopic Mass 180.974 Da
Topological Polar Surface Area 52.300 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 91.700
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 2

Citations of This Product

1. Yuguang Wang, Mengjing Wu, Huifang Zheng, Dongmei Wu, Panpan Yao, Wenjing Li, Kexin Jin, Xinjun Yu.  (2024)  Biomanufacture of L-homoserine lactone building block: A strategy for preparing γ-substituted L-amino acids by modular reaction.  ENZYME AND MICROBIAL TECHNOLOGY,  176  (110411). 

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