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1,6-DIAMINO(HEXANE-1,1,6,6-D4), also known as 1,6-Hexane-1,1,6,6-d4-diamine, is an isotopically labeled research compound with the CAS number 115797-49-4. It is a derivative of hexane with two amine groups and deuterium atoms at specific positions, which makes it valuable for various research applications.

115797-49-4

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115797-49-4 Usage

Uses

1. Used in Research Applications:
1,6-DIAMINO(HEXANE-1,1,6,6-D4) is used as a research compound for studying the effects of isotopic labeling on chemical reactions and molecular interactions. Its isotopically labeled nature allows researchers to track and analyze the behavior of molecules in various chemical and biological processes.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,6-DIAMINO(HEXANE-1,1,6,6-D4) can be used as a building block or a precursor for the synthesis of isotopically labeled drugs. These labeled drugs can be utilized in drug metabolism studies, pharmacokinetic research, and the development of new therapeutic agents.
3. Used in Chemical Synthesis:
1,6-DIAMINO(HEXANE-1,1,6,6-D4) can be employed as a starting material or an intermediate in the synthesis of various isotopically labeled organic compounds. These compounds can be used in a wide range of applications, including the development of new materials, catalysts, and chemical sensors.
4. Used in Analytical Chemistry:
In analytical chemistry, 1,6-DIAMINO(HEXANE-1,1,6,6-D4) can be used as an internal standard or a reference compound for the quantification and identification of target molecules in complex samples. Its unique isotopic signature can help improve the accuracy and precision of analytical measurements.
5. Used in Environmental Studies:
1,6-DIAMINO(HEXANE-1,1,6,6-D4) can be utilized in environmental research to study the fate and transport of pollutants, as well as the behavior of contaminants in various environmental matrices. Its isotopically labeled nature can provide valuable insights into the environmental impact of chemicals and their degradation pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 115797-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,9 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115797-49:
(8*1)+(7*1)+(6*5)+(5*7)+(4*9)+(3*7)+(2*4)+(1*9)=154
154 % 10 = 4
So 115797-49-4 is a valid CAS Registry Number.

115797-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,6,6-tetradeuteriohexane-1,6-diamine

1.2 Other means of identification

Product number -
Other names 1,6-Hexane-1,1,6,6-d4-diamine,Hexamethylene-1,1,6,6-d4-diamine

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:115797-49-4 SDS

115797-49-4Downstream Products

115797-49-4Relevant academic research and scientific papers

Ruthenium catalyzed deuterium labelling of α-carbon in primary alcohol and primary/secondary amine in D2O

Takahashi, Masaaki,Oshima, Koichiro,Matsubara, Seijiro

, p. 192 - 193 (2005)

Primary alcohols and primary/secondary amines are labelled with D atom at α-position regioselectively by means of deuterium oxide and ruthenium catalyst. Copyright

Ultrasound-assisted reduction of cyanides to deuteriated aliphatic amines

Tsuzuki, Hirohisa,Harada, Toshinao,Mukumoto, Mamoru,Mataka, Shuntaro,Tsukinoki, Takehito,Kakinami, Takaaki,Nagano, Yoshiaki,Tashiro, Masashi

, p. 385 - 393 (2007/10/03)

In the presence of ultrasound various mono-, di-, and α,β-unsaturated cyanides were reduced with Cu-Al alloy in NaOD-D2O and THF to the corresponding deuteriated aliphatic amines, such as nonylamines, Putrescine, and 1,6-hexanediamine, in high deuterium content.

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