Welcome to LookChem.com Sign In|Join Free
  • or
H-ARG-ARG-ARG-OH ACETATE SALT is a chemical compound derived from the amino acid arginine, consisting of three arginine molecules linked together and combined with an acetate group. It possesses potential therapeutic applications due to its ability to enhance nitric oxide production, improve blood flow, and exhibit neuroprotective and antioxidant properties, making it a promising candidate for various medical and pharmaceutical uses.

6418-87-7

Post Buying Request

6418-87-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6418-87-7 Usage

Uses

Used in Cardiovascular Health Applications:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a cardiovascular health enhancer for its ability to improve blood flow, which can benefit individuals with conditions such as hypertension.
Used in Athletic Performance Applications:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a performance booster for athletes, as its nitric oxide-enhancing properties can improve blood flow and oxygen delivery to muscles, potentially increasing endurance and reducing fatigue.
Used in Wound Healing Applications:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a wound healing agent due to its ability to improve blood flow to the affected area, promoting faster healing and recovery.
Used in Neuroprotection Applications:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a neuroprotective agent for its potential to protect neurons from damage and degeneration, which may be beneficial in treating neurological disorders.
Used in Antioxidant Applications:
H-ARG-ARG-ARG-OH ACETATE SALT is used as an antioxidant to combat oxidative stress and protect cells from damage, which may have implications in preventing or treating various diseases and conditions.
Used in Erectile Dysfunction Treatment:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a treatment for erectile dysfunction, as its ability to improve blood flow can help enhance erectile function in men with this condition.
Used in Diabetic Complications Prevention:
H-ARG-ARG-ARG-OH ACETATE SALT is used as a preventive measure for diabetic complications, as its potential benefits in improving blood flow and reducing oxidative stress may help protect against the development of complications associated with diabetes.

Check Digit Verification of cas no

The CAS Registry Mumber 6418-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6418-87:
(6*6)+(5*4)+(4*1)+(3*8)+(2*8)+(1*7)=107
107 % 10 = 7
So 6418-87-7 is a valid CAS Registry Number.

6418-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name H-Arg-Arg-Arg-OH

1.2 Other means of identification

Product number -
Other names triarginine

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:6418-87-7 SDS

6418-87-7Downstream Products

6418-87-7Relevant academic research and scientific papers

Modelling of prebiotic synthesis and selection of peptides under isothermal conditions and thermal cycling mode

Demina,Kononikhin,Laptev,Khodonov,Nikolaev,Varfolomeev

, p. 422 - 441 (2013/06/27)

The model peptide synthesis from mixtures of amino acids was carried out under the thermal cycling and isothermal modes. The compositions of the obtained mixtures of products and the primary amino acid sequence of the synthesized peptides were determined by Fourier transform ion cyclotron resonance mass spectrometry and tandem mass spectrometry in combination with high-performance liquid chromatography with the application of de novo sequencing of the synthesized products. The processes of abiogenous synthesis of peptides were shown to occur under relatively mild temperature conditions and give a substantially less number of peptides as compared with the possible statistical set. The evolution of the system takes place in the process of the synthesis in solid phase with the disappearance of a series of the most unstable peptides. The selection process with the formation of complementary peptides takes place in peptide synthesis under the thermal cyclic mode.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6418-87-7