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(E)-(4-chlorophenyl)diazenecarbonitrile, commonly known as DNCB, is a chemical compound characterized by its yellow crystalline structure. It is insoluble in water but readily soluble in organic solvents. DNCB is predominantly utilized in the industrial production of dyes and pigments, particularly in the textile sector for the creation of azo dyes and pigments. Additionally, it serves as a key intermediate in the chemical synthesis of various other compounds.

33554-72-2

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33554-72-2 Usage

Uses

Used in Textile Industry:
(E)-(4-chlorophenyl)diazenecarbonitrile is used as a key intermediate for the production of azo dyes and pigments in the textile industry. Its application is primarily due to its ability to impart vibrant colors and hues to fabrics, enhancing their visual appeal and durability.
Used in Chemical Synthesis:
DNCB is also employed as a crucial component in the synthesis of other chemical compounds. Its versatile chemical structure allows for its use in creating a wide range of products, contributing to its significance in the chemical industry.
Used in Dye and Pigment Production:
(E)-(4-chlorophenyl)diazenecarbonitrile is used as a raw material in the production of dyes and pigments. Its application in this industry is driven by its capacity to produce a diverse array of colors, making it a valuable asset for creating visually striking and long-lasting dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 33554-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,5 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33554-72:
(7*3)+(6*3)+(5*5)+(4*5)+(3*4)+(2*7)+(1*2)=112
112 % 10 = 2
So 33554-72-2 is a valid CAS Registry Number.

33554-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chlorophenyl)iminocyanamide

1.2 Other means of identification

Product number -
Other names -

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:33554-72-2 SDS

33554-72-2Upstream product

33554-72-2Downstream Products

33554-72-2Relevant academic research and scientific papers

Arylazoamidoximes and related compounds as NO-modulators

Schroeder, Alexander,Kotthaus, Juerke,Schade, Dennis,Clement, Bernd,Rehse, Klaus

experimental part, p. 9 - 16 (2010/07/03)

Three amidinoarylhydrazines 1, three arylazoamidines 2, and nine arylazoamidoximes 3 have been synthesized and investigated for their potential to function as nitric oxide (NO) modulators. In-vitro studies demonstrated that 2 and 3 inhibited platelet aggregation (2c, IC50 = 3 μM) which could also be shown in vivo by inhibition of thrombus formation in arterioles (3a, 22%). Moreover, for all compounds antihypertensive effects were examined in vivo with SHR rats, with 2a being the most potent candidate by lowering blood pressure by 19%. However, no common underlying mechanism of action could be shown. Some of these compounds released HNO non-enzymatically. Incubations with NO synthase isoforms (NOSs) revealed, that compounds 1 to 3 were weak substrates for NOSs but arylazoamidoximes 3 remarkably elevated the NOSs activity in the presence of L-arginine (3h, up to fivefold). In addition, we examined effects on arginase and dimethylarginine dimethylaminohydrolase (DDAH), two further enzymes involved in the complex regulation of NO biosynthesis, to elucidate whether the observed in-vivo effects can be traced back to their modulation. Furthermore, the metabolic fate of arylazoamidoximes 3 was addressed by investigation of a possible N-reductive biotransformation. In summary, novel NO-modulating compound classes are presented, among which arylazoamidoximes 3 are potent activators of NOS isoforms, and arylazoamidines 2 exert in-vivo effects by unknown mechanisms.

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