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19022-06-1

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19022-06-1 Usage

Chemical composition

2-(3,5-dinitrophenyl)-1H-benzimidazole consists of a benzimidazole ring with a dinitrophenyl group attached to one of its positions.

Reagent use

It is a widely used reagent for detecting and quantifying aldehydes and ketones in various chemical samples.

Reaction

DNPH-benzimidazole reacts with the carbonyl functional group present in aldehydes and ketones, resulting in the formation of a yellow to orange precipitate.

Identification and measurement

The yellow to orange precipitate allows for the identification and measurement of aldehydes and ketones.

Importance in analytical chemistry

DNPH-benzimidazole is an important tool in analytical chemistry, particularly in the field of environmental and occupational health.

Applications

It is often utilized to assess the presence of volatile organic compounds and harmful chemicals in air and other environmental samples.

Check Digit Verification of cas no

The CAS Registry Mumber 19022-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19022-06:
(7*1)+(6*9)+(5*0)+(4*2)+(3*2)+(2*0)+(1*6)=81
81 % 10 = 1
So 19022-06-1 is a valid CAS Registry Number.

19022-06-1SDS

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 2-(3,5-dinitrophenyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-(3,5-dinitrophenyl)-benzimidazole

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:19022-06-1 SDS

19022-06-1Relevant articles and documents

Chiral bio-nanocomposites based on thermally stable poly(amide-imide) having phenylalanine linkages and reactive organoclay containing tyrosine amino acid

Mallakpour, Shadpour,Dinari, Mohammad

, p. 1021 - 1029 (2013/07/27)

Montmorillonite clay modified with the bio-active trifunctional l-tyrosine amino acid salt was used as a reactive organoclay (OC) for the preparation of poly(amide-imide) (PAI)/OC hybrid films. One of the functional groups of the l-tyrosine as the swelling agent formed an ionic bond with the negatively charged silicates, whereas the remaining functional groups were available for further reaction with polymer matrix. The soluble PAI with amine end groups including phenylalanine amino acid was synthesised under green condition using molten tetra-butylammonium bromide by direct polymerization reaction of chiral diacid and 2-(3,5-diaminophenyl)benzimidazole. PAI/OC bio-nanocomposites films containing different contents of OC were prepared via solution intercalation method through blending of OC with the PAI solution. X-ray diffraction and transmission electron microscopy revealed that the dispersion of silicate layers in the PAI created an exfoliated structure as a result of using the trifunctional groups of the swelling agent. The structure and thermal behavior of the synthesised materials were characterized by a range of methods, including X-ray diffraction, Fourier transform infrared spectroscopy, 1H-NMR, electron microscopy, elemental and thermogravimetric analysis techniques. Thermogravimetric analysis results indicated that the addition of OC into the PAI matrix was increased in the thermal decomposition temperatures of the resulted bio-nanocomposites.

Investigating the nanostructure and thermal properties of chiral poly(amide-imide)/Al2O3 compatibilized with 3-aminopropyltriethoxysilane

Mallakpour, Shadpour,Dinari, Mohammad

, p. 3865 - 3872 (2013/09/02)

Novel chiral poly(amide-imide) (PAI)/Al2O3 nanocomposites were prepared via incorporating surface modified Al 2O3 nanoparticles into polymer matrices for the first time. In the process of preparing the nanocomposites, severe aggregation of Al2O3 nanoparticles could be reduced by surface modification and γ-aminopropyltriethoxysilane. The optically active PAI chains were formed from the polycondensation reaction of N,N′- (pyromellitoyl)-bis-phenylalanine diacid with 2-(3,5-diaminophenyl)- benzimidazole in green condition. The obtained polymer and inorganic metal oxide nanoparticles were used to prepare chiral PAI/Al2O3 nanocomposites through ultrasonic irradiation. The resulting nanoparticle filled composites were also characterized by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy and thermogravimetric analysis (TGA) techniques. TGA thermographs confirmed that the heat stability of the prepared nanoparticle-reinforced composites was improved. Mechanical properties showed that the film containing 10 wt% of modified Al2O3 had a tensile strength of the order of 83.6 MPa, relative to the 64.3 MPa of the pure PAI.

Synthesis, characterization and fuel cell application of polyimides

Lee, Minju,Khan, Sher B.,Seo, Kwangwon,Lee, Jin-Woo,Akhtar, Kalsoom,Han, Haksoo,Asiri, Abdullah M.

, p. 655 - 659 (2013/03/13)

Proton conducting polyimides containing pendant benzimidazole groups have been synthesized by different ratios of 5-(1H-benzimidazol-2-yl)-benzene-1-3- diamine (DABI) and oxydianiline (ODA) in the presence of oxydianiline (ODPA). All the polymers were str

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