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4-(4-Butylphenylazo)phenol, a member of the azo compounds, is a chemical compound known for its vibrant red color and stable properties. It is characterized by its red powder form and insolubility in water. With a molecular formula of C18H18N2O and a molecular weight of 282.35 g/mol, 4-(4-BUTYLPHENYLAZO)PHENOL is widely recognized for its use in coloring textiles and food products, although it requires careful handling due to potential health and environmental concerns.

2496-21-1

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2496-21-1 Usage

Uses

Used in Textile Industry:
4-(4-Butylphenylazo)phenol is used as a dye in the textile industry for its ability to impart a vibrant and stable red color to fabrics. Its colorfastness and resistance to fading make it a popular choice for various textile applications.
Used in Food Industry:
In the food industry, 4-(4-Butylphenylazo)phenol serves as a coloring agent to add a rich red hue to food products. Its stable coloration ensures that the food maintains its visual appeal even under various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 2496-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2496-21:
(6*2)+(5*4)+(4*9)+(3*6)+(2*2)+(1*1)=91
91 % 10 = 1
So 2496-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H18N2O/c1-2-3-4-13-5-7-14(8-6-13)17-18-15-9-11-16(19)12-10-15/h5-12,19H,2-4H2,1H3

2496-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-butylphenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 1. 4-butyl-4'-hydroxyazobenzene

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:2496-21-1 SDS

2496-21-1Relevant academic research and scientific papers

Azobenzene molecular material with photoinduced solid-liquid conversion characteristic and synthesis method and application of azobenzene molecular material

-

Paragraph 0036-0041, (2021/01/11)

The invention relates to an azobenzene molecular material with a photoinduced solid-liquid conversion characteristic and a synthesis method and application thereof. The azobenzene molecular material has a structure as shown in a formula I which is describ

Reversible Micrometer-Scale Spiral Self-Assembly in Liquid Crystalline Block Copolymer Film with Controllable Chiral Response

Yuan, Jianan,Lu, Xuemin,Li, Qingxiang,Lü, Zhiguo,Lu, Qinghua

supporting information, p. 12308 - 12312 (2021/04/26)

The spiral is a fundamental structure in nature and spiral structures with controllable handedness are of increasing interest in the design of new chiroptical materials. In this study, micrometer-scale spiral structures with reversible chirality were fabr

Branched Aggregates with Tunable Morphology via Hierarchical Self-Assembly of Azobenzene-Derived Molecular Double Brushes

Lin, Shaoliang,Qian, Hongyu,Xu, Binbin,Zhang, Ling

, p. 17707 - 17713 (2021/07/12)

Hierarchical self-assembly is one of the most effective approaches to fabricate nature-inspired materials with subtle nanostructures. We report a distinct hierarchical self-assembly process of molecular double brushes (MDBs) with each graft site carrying

CO2 /N2 Light double-stimulus-responsive surfactant and synthetic method thereof

-

Paragraph 0017; 0033; 0034, (2017/08/25)

The invention relates to a CO2/N2-light dual-stimulus-response type surfactant, and belongs to the field of colloid and interfacial chemistry. The surfactant is an azobenzene bicarbonate surfactant prepared by using 4-alkylaniline and phenol as raw materi

Containing azo phenyl the xylosides and its preparation method and application

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Paragraph 0101-0104, (2017/05/02)

The invention belongs to the field of catalytic reaction engineering, and particularly relates to synthetic glucoside containing an azobenzene group, and application of the glucoside serving as an ultraviolet controlled-release material. The glucoside containing an azobenzene group has a structure as shown in Formula (I). The glucoside containing an azobenzene group can be used for preparation of ultraviolet sensitive liposome, and has favorable structural stability, biological targeting property, biocompatibility and in-vivo degradability.

A self-healing photoinduced-deformable material fabricated by liquid crystalline elastomers using multivalent hydrogen bonds as cross-linkers

Ni, Bin,Xie, He-Lou,Tang, Jun,Zhang, Hai-Liang,Chen, Er-Qiang

supporting information, p. 10257 - 10260 (2016/08/23)

Liquid crystalline elastomers (LCEs) using multivalent hydrogen bonds as cross-linkers were successfully fabricated, which showed both self-healing and photoinduced-deformable properties. More interestingly, this LCE could be readily molded into different

Photochromic and nonlinear optical properties of azo-functionalized POSS nanoparticles dispersed in nematic liquid crystals

Miniewicz, Andrzej,Girones, Julie,Karpinski, Pawel,Mossety-Leszczak, Beata,Galina, Henryk,Dutkiewicz, Michal

, p. 432 - 440 (2014/01/06)

It is well known that addition of a small amount of nanoparticles to liquid crystals may enhance their nonlinear optical properties. To date, in most reports, semiconductor- or metallic-core nanoparticles in LCs have been described. Here, we report on the

Micellar catalysis using a photochromic surfactant: Application to the pd-catalyzed tsuji-trost reaction in water

Billamboz, Muriel,Mangin, Floriane,Drillaud, Nicolas,Chevrin-Villette, Carole,Banaszak-Leonard, Estelle,Len, Christophe

, p. 493 - 500 (2014/04/03)

The first example of a Pd-catalyzed Tsuji-Trost reaction, applied in a photochromic micellar media under conventional heating and microwave irradiation, is reported. The surfactant activity and recycling ability were investigated and compared with those of a few commercially available surfactants. The synthetic photochromic surfactant proved to be efficient, recyclable, and versatile for Pdcatalyzed coupling reactions.

Chiral self-assembly of designed amphiphiles: Optimization for nanotube formation

Barclay, Thomas G.,Constantopoulos, Kristina,Matisons, Janis G.,Zhang, Wei,Fujiki, Michiya

, p. 14172 - 14179,8 (2020/09/02)

Four amphiphiles with l-aspartic acid headgroups (Asp) and a diphenyldiazenyl group (Azo) contained within the hydrophobic tails were designed and synthesized for self-assembly into helically based nanotubes. The amphiphiles of the form R'-{4-[(4-alkylphenyl)diazenyl]phenoxy}alkanoyl-l- aspartic acid (where R' is 10 or 11) varied only in alkyl chain lengths either side of the azo group, having 4, 7, or 10 carbon distal chains and 10 or 11 carbon proximal chains (R-Azo-R'-Asp, where R denotes the number of carbons in the distal chain and R' denotes the number of carbons in the proximal chain). Despite the molecular similarities, distinct differences were identified in the chiral order of the structures self-assembled from hot methanolic aqueous solutions using microscopy and spectroscopic analyses. This was reflected in dominant thermodynamic aggregate morphologies that ranged from amorphous material for 10-Azo-10-Asp, through twisted ribbons (196 ± 49 nm pitch) for 7-Azo-11-Asp, to the desired helically based nanotubes for 4- and 7-Azo-10-Asp (81 ± 11 and 76 ± 6 nm diameters, respectively). Another key variable in the self-assembly of the amphiphiles was the use of a second method to precipitate aggregates from solution at room temperature. This method enabled the isolation of thermodynamically unstable and key transitional structures. Helical ribbons were precursor structures to the nanotubes formed from 4- and 7-Azo-10-Asp as well as the wide, flattened nanotube structures (587 ± 85 nm width) found for 4-Azo-10-Asp. Overall, the results highlighted the interplay of influence of the headgroup and the hydrophobic tail on self-assembly, providing a basis for future rational design of self-assembling amphiphiles.

Synthesis, characterization and thermal and photo alignment behavior of polyethylene imines having butyl substituent azobenzene side chain group

Kamruzzaman, Mohammad,Kuwahara, Yutaka,Ogata, Tomonari,Ujiie, Seiji,Kurihara, Seiji

experimental part, p. 134 - 148 (2012/04/23)

New type of polyethylene imine having butyl (-C4H9) substituent azobenzene side chain group through methylene spacer group (PEI64) was successfully synthesized by solution polycondensation reaction. Synthesized polymer was characteri

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