Product Added to Cart!
$91.10

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI21652_1_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
DL-2,4-Diaminobutyric acid dihydrochloride
Brand Name
Chem Impex
Product Number
21652
CAS
65427-54-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2724329
IUPAC Name
2,4-diaminobutanoic acid;dihydrochloride
InChI Key
CKAAWCHIBBNLOJ-UHFFFAOYSA-N
SMILES
C(CN)C(C(=O)O)N.Cl.Cl

Description

DL-2,4-Diaminobutyric acid dihydrochloride is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.

Biochemical Research: It is used in studies related to amino acid metabolism and protein synthesis, aiding researchers in understanding cellular functions and metabolic pathways.

Neuroscience Studies: The compound is explored for its potential neuroprotective effects, making it valuable in research aimed at developing treatments for neurodegenerative diseases.

Food Industry: It can be applied as a nutritional supplement, contributing to formulations aimed at improving amino acid profiles in food products, thus enhancing their health benefits.

Cosmetic Formulations: The compound is investigated for its potential in skin care products, where it may help in promoting skin health and improving the appearance of aging skin.

References Data Source From Pubchem

Occurrence of β-N-Methylamino-L-Alanine (BMAA) Toxin in irrigation Water and Field Vegetable Plants and Assessing Its Potential Risk to Human Health

Publication Name: Water, Air, & Soil Pollution
Publication Date: 2024-01
DOI: 10.1007/s11270-023-06861-0

Quantitative determination of the neurotoxin β-N-methylamino-l-alanine (BMAA) by capillary electrophoresis–tandem mass spectrometry

Publication Name: Analytical and Bioanalytical Chemistry
Publication Date: 2016-12-01
DOI: 10.1007/s00216-016-0091-y

Development of an analytical procedure for quantifying the underivatized neurotoxin β-N-methylamino-l-alanine in brain tissues

Publication Name: Analytical and Bioanalytical Chemistry
Publication Date: 2014-05-25
DOI: 10.1007/s00216-014-7872-y

Vesicular and carrier-mediatied depolarization-induced release of [3H]GABA: Inhibition by amiloride and verapamil

Publication Name: Neurochemical Research
Publication Date: 1993-10
DOI: 10.1007/bf00966688