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H-HIS-PRO-NH2 2 HBR is a chemical compound that consists of histidine-proline amide with two molecules of hydrobromic acid. This peptide is formed by the connection of the amino acids histidine and proline through an amide bond. It is widely utilized in the fields of biochemistry and research as a model peptide for understanding the structure and function of proteins. The incorporation of hydrobromic acid leads to the formation of a hydrobromide salt, which can significantly affect the solubility, stability, and other properties of the peptide in various experimental conditions. H-HIS-PRO-NH2 2 HBR is an indispensable compound for exploring the behavior of peptides and their interactions with other molecules.

59760-04-2

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59760-04-2 Usage

Uses

Used in Biochemistry Research:
H-HIS-PRO-NH2 2 HBR is used as a model peptide for studying the structural and functional aspects of proteins. It aids in understanding the fundamental principles of protein folding, stability, and interactions with other molecules.
Used in Pharmaceutical Development:
H-HIS-PRO-NH2 2 HBR is utilized in the development of pharmaceuticals, particularly for designing peptide-based drugs. Its unique properties and interactions with other molecules make it a valuable compound for drug discovery and optimization.
Used in Material Science:
In the field of material science, H-HIS-PRO-NH2 2 HBR is employed in the development of biomaterials and peptide-based materials. Its ability to form hydrobromide salts can influence the properties of these materials, making them suitable for various applications, such as drug delivery systems and tissue engineering.
Used in Analytical Chemistry:
H-HIS-PRO-NH2 2 HBR is used as a reference compound in analytical chemistry for the development and validation of analytical methods. Its well-defined structure and properties make it an ideal candidate for assessing the performance of chromatographic, spectroscopic, and other analytical techniques.
Used in Education and Training:
H-HIS-PRO-NH2 2 HBR serves as an educational tool in academic and training programs related to biochemistry, molecular biology, and pharmaceutical sciences. It helps students and researchers gain hands-on experience in working with peptides and understanding their properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 59760-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59760-04:
(7*5)+(6*9)+(5*7)+(4*6)+(3*0)+(2*0)+(1*4)=152
152 % 10 = 2
So 59760-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N5O2.2BrH/c12-8(4-7-5-14-6-15-7)11(18)16-3-1-2-9(16)10(13)17;;/h5-6,8-9H,1-4,12H2,(H2,13,17)(H,14,15);2*1H/t8-,9-;;/m0../s1

59760-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]pyrrolidine-2-carboxamide,dihydrobromide

1.2 Other means of identification

Product number -
Other names L-Histidyl-L-prolinamide dihydrobromide

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:59760-04-2 SDS

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