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2-aminodecanoic acid, hydrochloride is a chemical compound with the formula C10H21NO2·HCl. It is a derivative of 2-aminodecanoic acid, where the carboxylic acid group has been protonated to form the hydrochloride salt. 2-aminodecanoic acid,hydrochloride is a white crystalline solid and is soluble in water. It is used as a building block in the synthesis of various pharmaceuticals and biologically active molecules, particularly in the preparation of peptides and other amino acid derivatives. The hydrochloride salt form enhances the solubility and stability of the compound, making it more suitable for certain applications in the pharmaceutical industry.

5463-27-4

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5463-27-4 Usage

Chemical compound

2-aminodecanoic acid, hydrochloride

Composition

Consists of a decanoic acid molecule with an amino group attached at the 2-position and a hydrochloride salt

Appearance

White, crystalline solid

Solubility

Soluble in water

Uses

Biochemical research
Additive in pharmaceutical preparations
Treatment of certain neurological disorders
Development of antiviral drugs
Chelating agent in chemical and industrial processes

Potential

Wide range of potential uses and of interest to researchers and industries in several fields

Check Digit Verification of cas no

The CAS Registry Mumber 5463-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5463-27:
(6*5)+(5*4)+(4*6)+(3*3)+(2*2)+(1*7)=94
94 % 10 = 4
So 5463-27-4 is a valid CAS Registry Number.

5463-27-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminodecanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-amino-decanoic acid,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5463-27-4 SDS

5463-27-4Downstream Products

5463-27-4Relevant academic research and scientific papers

Pro-apoptotic activity of lipidic α-amino acids isolated from Protopalythoa variabilis

Wilke, Diego Veras,Jimenez, Paula Christine,Araújo, Renata Mendona,Da Silva, Wildson Max Barbosa,Pessoa, Otília Deusdênia Loiola,Silveira, Edilberto Rocha,Pessoa, Claudia,De Moraes, Manoel Odorico,Skwarczynski, Mariusz,Simerska, Pavla,Toth, Istvan,Costa-Lotufo, Letícia Veras

scheme or table, p. 7997 - 8004 (2011/02/23)

Lipidic α-amino acids (LAAs) have been described as non-natural amino acids with long saturated or unsaturated aliphatic chains. In the continuing prospect to discover anticancer agents from marine sources, we have obtained a mixture of two cytotoxic LAAs (1a and 1b) from the zoanthid Protopalythoa variabilis. The anti-proliferative potential of 14 synthetic LAAs and 1a/1b were evaluated on four tumor cell lines (HCT-8, SF-295, MDA-MB-435, and HL-60). Five of the synthetic LAAs showed high percentage of tumor cell inhibition, while 1a/1b completely inhibited tumor cell growth. Additionally, apoptotic effects of 1a/1b were studied on HL-60 cell line. 1a/1b-treated cells showed apoptosis morphology, loss of mitochondrial potential, and DNA fragmentation.

Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase

Kim, In-Hae,Nishi, Kosuke,Tsai, Hsing-Ju,Bradford, Tanya,Koda, Yasuko,Watanabe, Takaho,Morisseau, Christophe,Blanchfield, Joanne,Toth, Istvan,Hammock, Bruce D.

, p. 312 - 323 (2008/02/04)

The soluble epoxide hydrolase (sEH) plays an important role in the metabolism of endogenous chemical mediators involved in blood pressure regulation and vascular inflammation. 12-(3-Adamantan-1-yl-ureido)-dodecanoic acid (AUDA, 1) is a very active inhibit

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