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1,5-Pentane-1,1,5,5-d4-diamine is a deuterated chemical compound that serves as a valuable building block in various applications, particularly in the field of chemical analysis and research.

95596-35-3

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95596-35-3 Usage

Uses

Used in Chemical Analysis:
1,5-Pentane-1,1,5,5-d4-diamine is used as a deuterated building block for the analysis of polyamines in rats. Its deuterated nature provides a distinct advantage in analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, by enhancing the resolution and sensitivity of the measurements. This allows for more accurate and reliable identification and quantification of polyamines, which are essential for understanding their biological roles and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 95596-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95596-35:
(7*9)+(6*5)+(5*5)+(4*9)+(3*6)+(2*3)+(1*5)=183
183 % 10 = 3
So 95596-35-3 is a valid CAS Registry Number.

95596-35-3SDS

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 1,5-PENTANE-1,1,5,5-D4-DIAMINE

1.2 Other means of identification

Product number -
Other names 1,5-naphthalendiamine

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:95596-35-3 SDS

95596-35-3Upstream product

95596-35-3Downstream Products

95596-35-3Relevant academic research and scientific papers

Gas chromatography mass spectrometry analysis of polyamines using deuterated analogs as internal standards.

Smith,Daves Jr.

, p. 146 - 151 (1977)

Quantitative analyses of subnanomole quantities of the polyamines putrescine, cadaverine, spermidine and spermine by the gas chromatography mass spectrometry technique of selected ion monitoring are complicated by effects of the chromatographic column. These effects include sample retention by the column and chromatographic band broadening, and are sufficiently serious that spermine (as the trifluoroacetylated derivative) was not detectable at levels below 50 picomoles. Because the chromatographic behaviors of the four polyamines vary, quantiative analysis using a single internal standard is not feasible. The deuterated polyamine analogs, putrescine-2H4, cadaverine-2H4, spermidine-2H6 and spermine-2H8, have been synthesized and used to accomplish quantiative analyses of the corresponding isotopically natural abundance polyamines to the one picomole level. This enhancement in analytical sensitivity is accomplished by use of large excesses (greater than or equal to 100 picomoles) of the deuterated analogs to improve chromatographic band profiles. The use of such large molar excesses of deuterated analogs for selected ion monitoring analyses is possible because their electron impact spectra exhibit high mass ions ([M-F3C]+, [M-F3CCO]+) which possess greater than or equal to 4 deuterium atoms and have intensity ratios (I2H(max):IH) of 500 or greater.

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