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2074-05-7

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2074-05-7 Usage

General Description

HEPTALDEHYDE (DNPH DERIVATIVE) is a chemical compound that is derived from the reaction of heptaldehyde with 2,4-dinitrophenylhydrazine (DNPH). It is used as a reagent in analytical chemistry for the detection and quantification of aldehydes and ketones. The DNPH derivative of heptaldehyde is used in various analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to identify and measure the levels of aldehydes in environmental samples, food products, and industrial chemicals. This derivative is known for its high sensitivity and selectivity in detecting aldehydes, making it a valuable tool in chemical analysis and environmental monitoring. Additionally, it is important to handle heptaldehyde (DNPH derivative) with caution due to its potential hazards, including skin and eye irritation, and it should be used in a well-ventilated area with appropriate personal protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 2074-05-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2074-05:
(6*2)+(5*0)+(4*7)+(3*4)+(2*0)+(1*5)=57
57 % 10 = 7
So 2074-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N4O4/c1-2-3-4-5-6-9-14-15-12-8-7-11(16(18)19)10-13(12)17(20)21/h7-10,15H,2-6H2,1H3

2074-05-7 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33848)  Heptanal2,4-dinitrophenylhydrazone  analytical standard

  • 2074-05-7

  • 33848-100MG

  • 1,326.78CNY

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2074-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name HEPTALDEHYDE (DNPH DERIVATIVE)

1.2 Other means of identification

Product number -
Other names Heptaldehyd-<2.4-dinitro-phenylhydrazon>

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:2074-05-7 SDS

2074-05-7Downstream Products

2074-05-7Relevant articles and documents

Visible-light mediated C-C bond cleavage of 1,2-diols to carbonyls by cerium-photocatalysis

Schwarz, Johanna,K?nig, Burkhard

supporting information, p. 486 - 488 (2019/01/10)

We describe a photocatalytic method for the cleavage of vicinal diols to aldehydes and ketones. The reaction is catalyzed by blue light and a cerium-catalyst and the scope includes aryl as well as alkyl substituted diols. The simple protocol which works under air and at room temperature enables the valorization of abundant diols.

A novel synthetic method for the preparation of aliphatic aldehydes from the corresponding carboxylic acids

Guo, Yuan,Lu, Zhenhuan,Yao, Libo,Shi, Zhen

, p. 489 - 492 (2012/01/05)

A novel synthetic method for the preparation of aliphatic aldehydes from the corresponding carboxylic acids via 1,3-dimethylbenzimidazolium salts is provided. 1,3-Dimethylbenzimidazolium salts were rapidly reduced with sodium/ethanol and then hydrolyzed with hydrochloric acid to obtain aliphatic aldehydes, in which the 1,3-dimethylbenzimidazolium salts can be readily achieved from the corresponding carboxylic acids. The mechanism for the reductive reaction of 1,3-dimethylbenzimidazolium salts with sodium/ethanol was discussed.

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