CAS 4961-40-4
:1,2-Ethanediamine, N1,N2-bis(2-aminoethyl)-, hydrochloride (1:4)
Description:
1,2-Ethanediamine, N1,N2-bis(2-aminoethyl)-, hydrochloride (1:4), commonly referred to as a derivative of ethylenediamine, is an organic compound characterized by its amine functional groups. It features two primary amine groups and is typically encountered as a hydrochloride salt, which enhances its solubility in water. This compound is often used in various applications, including as a chelating agent, in pharmaceuticals, and in the synthesis of other organic compounds. Its structure allows for multiple hydrogen bonding interactions, contributing to its reactivity and potential biological activity. The presence of multiple amino groups makes it a versatile building block in organic synthesis and a candidate for various chemical reactions, including acylation and alkylation. Additionally, due to its basic nature, it can interact with acids to form stable salts, which are often more manageable in laboratory settings. Safety considerations should be taken into account, as amines can be irritants and may pose health risks upon exposure.
Formula:C6H18N4·4ClH
InChI:InChI=1S/C6H18N4.4ClH/c7-1-3-9-5-6-10-4-2-8;;;;/h9-10H,1-8H2;4*1H
InChI key:InChIKey=OKHMDSCYUWAQPT-UHFFFAOYSA-N
SMILES:C(CNCCN)NCCN.Cl
Synonyms:- Cuprior
- Triethylenetetramine, tetrahydrochloride
- Trientine tetrahydrochloride
- 1,2-Ethanediamine, N,N′-bis(2-aminoethyl)-, tetrahydrochloride
- 1,2-Ethanediamine, N1,N2-bis(2-aminoethyl)-, hydrochloride (1:4)
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Found 9 products.
Triethylenetetramine Tetrahydrochloride
CAS:Formula:C6H18N4·4HClPurity:>60.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:292.07Triethylenetetramine tetrahydrochloride
CAS:Formula:C6H22Cl4N4Purity:97%Color and Shape:SolidMolecular weight:292.0777Trientine-d4 TetraHCl (Triethylenetetramine-d4 TetraHCl)
CAS:Formula:C6H14D4N4·4HClColor and Shape:White To Off-White SolidMolecular weight:150.26 4*36.46Trientine TetraHCl (Triethylenetetramine TetraHCl)
CAS:Formula:C6H18N4·4HClMolecular weight:146.24 4*36.46N1,N1-(Ethane-1,2-Diyl)Bis(Ethane-1,2-Diamine) Tetrahydrochloride
CAS:N1,N1-(Ethane-1,2-Diyl)Bis(Ethane-1,2-Diamine) TetrahydrochloridePurity:97%Molecular weight:292.08g/molTRIETHYLENETETRAMINE TETRAHCL
CAS:Formula:C6H22Cl4N4Purity:60.0%Color and Shape:SolidMolecular weight:292.07Triethylenetetramine-d4 Tetrahydrochoride
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Labelled analogue of Triethylenetetramine, a crosslinking agent.It is the labeled form of Triethylenetetramine Tetrahydrochoride (CAS#: 4961-40-4) used in preparation of Motuporamine derivatives, Cyclopentadecyl Polyamines and Cholic Acid derivatives as membrane-active antibiotic enhancers active against Gram-neg. multidrug-resistant species.<br>References Phanstiel, O., et al.: U.S. Pat. Appl. Publ., (2017);<br></p>Formula:C6H14D4N4•4(HCl)Color and Shape:NeatMolecular weight:150.2643646Triethylenetetramine Tetrahydrochloride
CAS:<p>Triethylenetetramine tetrahydrochloride (TETA) is a drug that has been shown to have the ability to enhance the immune system. It was first synthesized in 1894 by German chemist Emil Fischer, and has been used as an immunomodulator in the treatment of autoimmune diseases. TETA enhances the immune system by inhibiting an enzyme that is responsible for destroying lymphocytes, which are a type of white blood cell. The drug inhibits hydrochloric acid production in the stomach, which can be beneficial for people with cancer or ulcers. TETA binds to human serum proteins and inhibits uv absorption, binding constants, and human serum protein-dependent enzymes. This drug also inhibits hepatic function and pancreatic function due to its effects on liver cells and pancreatic cells respectively. TETA is classified as a non-competitive inhibitor because it does not compete with other substrates for access to an enzyme’s active site but rather binds at some distance</p>Formula:C6H18N4·4HClPurity:Min. 95%Molecular weight:292.07 g/mol







