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19764-96-6

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19764-96-6 Usage

Chemical Properties

yellow-brown glistening powder

Uses

Suitable as laser dye

Check Digit Verification of cas no

The CAS Registry Mumber 19764-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19764-96:
(7*1)+(6*9)+(5*7)+(4*6)+(3*4)+(2*9)+(1*6)=156
156 % 10 = 6
So 19764-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C29H33N2.HI/c1-28(2)22-16-12-14-18-24(22)30(5)26(28)20-10-8-7-9-11-21-27-29(3,4)23-17-13-15-19-25(23)31(27)6;/h7-21H,1-6H3;1H/q+1;/p-1

19764-96-6 Well-known Company Product Price

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  • Aldrich

  • (252034)  1,1′,3,3,3′,3′-Hexamethylindotricarbocyanineiodide  97%

  • 19764-96-6

  • 252034-100MG

  • 583.83CNY

  • Detail

19764-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1',3,3,3',3'-HEXAMETHYLINDOTRICARBOCYANINE IODIDE

1.2 Other means of identification

Product number -
Other names 1,7-Bis-(1,3,3-trimethyl-3H-indol-2-yl)-heptamethinium,Jodid

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:19764-96-6 SDS

19764-96-6Relevant articles and documents

Tuning the optoelectronic properties of cyanine and ketocyanine dyes by incorporation of 9,9-di-n-propylfluorenylindolenine

Jansen-Van Vuuren,Deakin,Olsen,Burn

, p. 1 - 8 (2014)

The synthesis and properties of novel cyanine and ketocyanine dyes incorporating 9,9-di-n-propylfluorenyl units is reported. While bathochromic shifts of order 100 nm are observed in cyanines for addition of each vinylene unit (lengthening the methine cha

N-alkylated linear heptamethine polyenes as potent non-azole leads against Candida albicans fungal infections

Critchley, Megan E.,Lawrence, Clare L.,McKenna, Sean T.,Okoh, Adeyi Okoh,Smith, Robert B.,Vishwapathi, Vinod

, (2020/07/21)

In this study, eighteen heptamethine dyes were synthesised and their antifungal activities were evaluated against three clinically relevant yeast species. The eighteen dyes were placed within classes based on their core subunit i.e. 2,3,3-trimethylindolenine (5a-f), 1,1,2-trimethyl-1H-benzo[e]indole (6a-f), or 2-methylbenzothiazole (7a-f). The results presented herein imply that the three families of cyanine dyes, in particular compounds 5a-f, show high potential as selective scaffolds to treat C. albicans infections. This opens up the opportunity for further optimisation and investigation of this class compounds for potential antifungal treatment.

Spectroscopic characterization of heptamethine cyanine dyes for the interaction with the CN- and F-

Wang, Yu,Gwon, Seon-Yeong,Son, Young-A,Kim, Sung-Hoon

, p. 61 - 66 (2013/09/02)

The selectivity and sensitivity of a benzoindolium heptamethine cyanine dyes toward CN- and F- in DMSO are described. These anions interact with Dye-1 and Dye-2 forming anion-Dye adducts, the formation of which was supported by the Pariser-Parr-Pople molecular orbital (PPP MO) calculation. The different optical responses in Dye-1 stimulated by addition of CN- (blue to pale yellow) and F' (blue to pink) allow simultaneous estimation of CN- and F-. Copyright Taylor and Francis Group, LLC.

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