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4‐[4‐(dimethylamino)phenyl]‐4,5‐dihydro‐3H‐1,2,4‐triazole‐3,5‐dione, also known as DAPTAD, is a Cookson-type reagent with a unique chemical structure that features a dimethylamino group attached to a phenyl ring, connected to a 1,2,4-triazole-3,5-dione moiety. 4‐[4‐(dimethylamino)phenyl]‐4,5‐dihydro‐3H‐1,2,4‐triazole‐3,5‐dione is known for its high sensitivity and specificity in chemical reactions.

111256-83-8

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111256-83-8 Usage

Uses

Used in Vitamin D3 Analysis:
4‐[4‐(dimethylamino)phenyl]‐4,5‐dihydro‐3H‐1,2,4‐triazole‐3,5‐dione is used as a derivatization agent for vitamin D3, specifically for the preparation of 25(OH)D3 samples in liquid chromatography-tandem mass spectrometry (LC-MS). It enhances the detection and quantification of vitamin D3 levels in biological samples, providing accurate and reliable results for assessing vitamin D status in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 111256-83-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111256-83:
(8*1)+(7*1)+(6*1)+(5*2)+(4*5)+(3*6)+(2*8)+(1*3)=88
88 % 10 = 8
So 111256-83-8 is a valid CAS Registry Number.

111256-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-(dimethylamino)phenyl]-1,2,4-triazole-3,5-dione

1.2 Other means of identification

Product number -
Other names 4-[4-(DIMETHYLAMINO)PHENYL]-3H-1,2,4-TRIAZOLE-3,5(4H)-DIONE

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:111256-83-8 SDS

111256-83-8Downstream Products

111256-83-8Relevant academic research and scientific papers

A novel Cookson-type reagent for enhancing sensitivity and specificity in assessment of infant vitamin D status using liquid chromatography/tandem mass spectrometry

Ogawa, Shoujiro,Ooki, Satoshi,Morohashi, Misato,Yamagata, Kenichiro,Higashi, Tatsuya

, p. 2453 - 2460 (2013)

Rationale 25-Hydroxyvitamin D3 [25(OH)D3] is the best-established indicator of vitamin D status. 4-Phenyl-1,2,4-triazoline-3,5- dione (PTAD), a representative Cookson-type reagent, has often been employed for enhancing the sensitivit

TRIAZOLINEDIONE ADDUCT, METHOD FOR PRODUCING TRIAZOLINEDIONE ADDUCT, METHOD FOR PRODUCING ENE COMPOUND, AND METHOD FOR ANALYZING ENE COMPOUND

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Paragraph 0263-0264, (2021/08/20)

Provided are a stable triazolinedione adduct, a method for producing the same, a method for producing an ene compound, and a method for analyzing an ene compound. A triazolinedione adduct that is stable until the time of use and can be reacted while reverting to a triazolinedione compound at the time of use. Specifically, a triazolinedione adduct represented by formula (1). (In the formula, R1 is an organic group, and A is a fused ring of three or more rings including at least one aromatic ring.)

METHOD FOR PRODUCING SOLID TRIAZOLINEDIONE COMPOUND, SOLID TRIAZOLINEDIONE COMPOUND, AND METHOD FOR PRODUCING TRIAZOLINEDIONE COMPOUND

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Paragraph 0104-0123; 0127-0129; 0135-0136; 0138; 0139; 0141, (2020/12/25)

Provided are a method for separating a DAPTAD-containing triazolinedione compound in solid form from a reaction solution, a separated solid triazolinedione compound, and a novel method for producing a triazolinedione compound. A triazolinedione solution in which a DAPTAD-containing triazolinedione compound is dissolved is brought into contact with a C5-15 hydrocarbon-based poor solvent to obtain a solid triazolinedione compound. Also, a triazolinedione compound is oxidized using an oxidizing agent that does not produce acid as a byproduct to obtain a triazolinedione compound.

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