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5-Amino caproic acid, also known as 5-aminohexanoic acid or epsilon-aminocaproic acid (EACA), is a synthetic amino acid with the chemical formula C6H13NO2. It is a white crystalline powder that is soluble in water and has a molecular weight of 131.17 g/mol. 5-AMINO CAPROIC ACID is primarily used as an antithrombotic agent, functioning as a lysine analog that inhibits fibrinolysis by blocking the action of plasmin, an enzyme responsible for breaking down blood clots. As a result, it is often administered in medical settings to prevent excessive bleeding during surgery or to treat conditions characterized by abnormal clot breakdown, such as hemophilia. Additionally, 5-amino caproic acid has been studied for its potential applications in various other medical and industrial fields, including the synthesis of pharmaceuticals and the treatment of certain kidney diseases.

628-47-7

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628-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 628-47-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 628-47:
(5*6)+(4*2)+(3*8)+(2*4)+(1*7)=77
77 % 10 = 7
So 628-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-5(7)3-2-4-6(8)9/h5H,2-4,7H2,1H3,(H,8,9)

628-47-7SDS

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 5-Aminohexanoic acid

1.2 Other means of identification

Product number -
Other names 5-Amino-hexansaeure

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:628-47-7 SDS

628-47-7Upstream product

628-47-7Downstream Products

628-47-7Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AS PRMT5 INHIBITORS

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Paragraph 082; 155; 195, (2020/12/11)

The present disclosure describes novel heterocyclic PRMT5 inhibitors and methods for preparing them. The pharmaceutical compositions comprising such PRMT5 inhibitors and methods of using them for treating cancer, infectious diseases, and other PRMT5 associated disorders are also described.

Scope and limitations of reductive amination catalyzed by half-sandwich iridium complexes under mild reaction conditions

Nguyen, Dat P.,Sladek, Rudolph N.,Do, Loi H.

supporting information, (2020/07/15)

The conversion of aldehydes and ketones to 1° amines could be promoted by half-sandwich iridium complexes using ammonium formate as both the nitrogen and hydride source. To optimize this method for green chemical synthesis, we tested various carbonyl substrates in common polar solvents at physiological temperature (37 °C) and ambient pressure. We found that in methanol, excellent selectivity for the amine over alcohol/amide products could be achieved for a broad assortment of carbonyl-containing compounds. In aqueous media, selective reduction of carbonyls to 1° amines was achieved in the absence of acids. Unfortunately, at Ir catalyst concentrations of 1 mM in water, reductive amination efficiency dropped significantly, which suggest that this catalytic methodology might be not suitable for aqueous applications where very low catalyst concentration is required (e.g., inside living cells).

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