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(3S)-1,8-diamino-4-azaoctane-1,1,2,3,5,5,6,6,7,7,8,8-d12 trihydrochloride, also known as N-(3-Aminopropyl)butane-1,4-diamine Trihydrochloride, is a chemical compound with a high purity of 95%. It is a labelled version of Spermidine Trihydrochloride and has been extensively studied in the context of polyamines. (3S)-1,8-diamino-4-azaoctane-1,1,2,3,5,5,6,6,7,7,8,8-d12 trihydrochloride has unique structural properties that allow it to interact with various ions, such as potassium and sodium, promoting different effects when binding with polyamines.

1173019-26-5

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1173019-26-5 Usage

Uses

Used in Structural and Functional Studies of Polyamines:
(3S)-1,8-diamino-4-azaoctane-1,1,2,3,5,5,6,6,7,7,8,8-d12 trihydrochloride is used as a research compound for studying the structural and functional aspects of polyamines. Its application in this field is due to its ability to interact with potassium and sodium ions, which promotes different effects when binding with polyamines, providing valuable insights into the role of polyamines in various biological processes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3S)-1,8-diamino-4-azaoctane-1,1,2,3,5,5,6,6,7,7,8,8-d12 trihydrochloride is used as a key compound in the development of new drugs targeting polyamine-related pathways. Its unique structural properties make it a promising candidate for the design and synthesis of novel therapeutic agents that can modulate polyamine interactions with ions, potentially leading to the development of new treatments for various diseases.
Used in Chemical Synthesis:
(3S)-1,8-diamino-4-azaoctane-1,1,2,3,5,5,6,6,7,7,8,8-d12 trihydrochloride is also used as a starting material or intermediate in the synthesis of various chemical compounds. Its unique structure and reactivity make it a valuable building block for the creation of new molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1173019-26-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,0,1 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1173019-26:
(9*1)+(8*1)+(7*7)+(6*3)+(5*0)+(4*1)+(3*9)+(2*2)+(1*6)=125
125 % 10 = 5
So 1173019-26-5 is a valid CAS Registry Number.

1173019-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(3-aminopropyl)-1,1,2,2,3,3,4,4-octadeuteriobutane-1,4-diamine,trihydrochloride

1.2 Other means of identification

Product number -
Other names -

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:1173019-26-5 SDS

1173019-26-5Upstream product

1173019-26-5Downstream Products

1173019-26-5Relevant academic research and scientific papers

Synthesis and conformation of deuterated spermidine for investigating weak interaction with polyanionic biomolecules

Maruyoshi, Keisuke,Demura, Tetsuo,Sagane, Takeshi,Matsumori, Nobuaki,Oishi, Tohru,Murata, Michio

, p. 5163 - 5170 (2004)

Polyamines such as spermidine and spermine are known to interact with polyanionic biomolecules under physiological conditions. Conformation analysis of these highly flexible acycles is virtually unprecedented due to the lack of appropriate methodologies.

Conformational change of spermidine upon interaction with adenosine triphosphate in aqueous solution

Maruyoshi, Keisuke,Nonaka, Kaori,Sagane, Takeshi,Demura, Tetsuo,Yamaguchi, Toshiyuki,Matsumori, Nobuaki,Oishi, Tohru,Murata, Michio

supporting information; experimental part, p. 1618 - 1626 (2009/09/29)

Endogenous polyamines, represented by putrescine, spermidine, and spermine, are known to exert their physiological functions by interacting with polyanionic biomolecules such as DNA, RNA, adenosine triphosphate (ATP), and phospholipids. Very few examples

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