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481634-76-8

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481634-76-8 Usage

Derivative of

1,3-Benzenediol (Resorcinol)

Structure

Two alkylamino groups attached to the fifth carbon

Common uses

a. Hair dyes and cosmetics as a colorant and antioxidant
b. Manufacturing of pharmaceuticals
c. Production of polymers
d. Chemical intermediate in organic synthesis

Potential applications

a. Antioxidant properties
b. Modifying physical and chemical properties of other substances

Safety precautions

Handle with care and follow safety guidelines due to potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 481634-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,6,3 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 481634-76:
(8*4)+(7*8)+(6*1)+(5*6)+(4*3)+(3*4)+(2*7)+(1*6)=168
168 % 10 = 8
So 481634-76-8 is a valid CAS Registry Number.

481634-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[bis(2-methylpropyl)amino]benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 3,5-dihydroxy-N,N-diisobutylaniline

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:481634-76-8 SDS

481634-76-8Downstream Products

481634-76-8Relevant articles and documents

Small-Molecule Absorber A1094 as a Stable and Fast-Clearing NIR-II Imaging Agent

Huang, Yanfang,Liu, Huanhuan,Chen, Xueyuan,Zhang, Yunming,Zhao, Xingyang,Huang, Wenchao,Mou, Zhaobiao,Wang, Chao,Zhang, Kaiqiang,Li, Zijing

, p. 2497 - 2503 (2021)

Photoacoustic imaging (PAI) in the second near-infrared window (NIR-II) is conducive to deep-tissue imaging due to small scattering coefficients, but often requires exogenous imaging agents. At present, nanoparticle-based NIR-II imaging agents are mainly used in non-clinical studies, some basic components of which are resistant to metabolism in vivo. The aim of this study was to examine the ~600 Da croconaine absorber A1094, absorbing lights around 1094 nm, as a rare, small-molecule NIR-II imaging agent in vivo. The clinical translational potential of A1094 injection were systematically revealed, including sufficient solubility and freeness in blood, good anti-interference ability, and favourable pH/oxidation-reduction/metabolic stabilities. After intravenous administration of A1094 injection, PAI of murine ears exhibited comparable capillaries visibility to that of PAI with popular Au nanorods. The contrasts achieved with A1094 and Au nanorods were 1.78 and 1.29 times higher than before administration, in the healthy group, and 3.25 and 1.58 times higher in the inflammation group. Notably, A1094 demonstrated a desired faster liver clearance than Au nanorods. The PAI signal of A1094 was cleared by 74.2 % after 3 h, whereas Au nanorods were only cleared by 43.1 %. The main metabolic mechanisms of A1094 were identified as N-methylation and lipid hydrolysis by murine liver microsomes in vitro. Therefore, A1094 may have promising clinical potential as a stable and fast-clearing NIR-II imaging agent.

An Activatable NIR-II Nanoprobe for In Vivo Early Real-Time Diagnosis of Traumatic Brain Injury

Li, Chunyan,Li, Wanfei,Liu, Huanhuan,Zhang, Yejun,Chen, Guangcun,Li, Zijing,Wang, Qiangbin

, p. 247 - 252 (2020)

Traumatic brain injury (TBI) is one of the most dangerous acute diseases resulting in high morbidity and mortality. Current methods remain limited with respect to early diagnosis and real-time feedback on the pathological process. Herein, a targeted activ

Electro-optical Properties of Neutral and Radical Ion Thienosquaraines

Maltese, Vito,Cospito, Sante,Beneduci, Amerigo,De Simone, Bruna Clara,Russo, Nino,Chidichimo, Giuseppe,Janssen, René A. J.

supporting information, p. 10179 - 10186 (2016/07/19)

Thienosquaraines are an interesting class of electroactive dyes that are useful for applications in organic electronics. Herein, the redox chemistry and electrochromic response of a few newly synthesized thienosquaraines are presented. These properties are compared to those of the commercial 2,4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl]squaraine. The stability of the radical ions formed in electrochemical processes strongly affects these properties, as shown by cyclic voltammetry, in situ spectroelectrochemistry, and quantum chemical calculations. Furthermore, all of the dyes show aggregation tendency resulting in panchromatic absorption covering the whole UV/Vis spectral range.

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