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14696-39-0

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  • 3H-Indolium,1-ethyl-2-[3-(1-ethyl-1,3-dihydro-3,3-dimethyl-2H-indol-2-ylidene)-1-propen-1-yl]-3,3-dimethyl-,iodide (1:1)

    Cas No: 14696-39-0

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14696-39-0 Usage

Chemical Properties

Deep Pueple Solid

Uses

A fluorescent dye.

Check Digit Verification of cas no

The CAS Registry Mumber 14696-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14696-39:
(7*1)+(6*4)+(5*6)+(4*9)+(3*6)+(2*3)+(1*9)=130
130 % 10 = 0
So 14696-39-0 is a valid CAS Registry Number.

14696-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1'-DIETHYL-3,3,3',3'-TETRAMETHYLINDOCARBOCYANINE IODIDE

1.2 Other means of identification

Product number -
Other names 1,1'-Diethyl-3,3,3',3'-tetramethylindocarbocyanine Iodide

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:14696-39-0 SDS

14696-39-0Downstream Products

14696-39-0Relevant articles and documents

Synthesis and physical performance of indole and benzimidazole cyanine dyes

Peng, Zheng-Hong

, p. 559 - 565 (1996)

Nine indole and benzimidazole cyanine dyes, used as green-sensitizing dyes in photographic emulsions, are synthesized. The compounds are characterized from mass spectrometric and NMR spectroscopic data, and elemental analysis. FAB mass spectrometry proved to be an efficient method for determining the structure of the compounds. From UV-VIS data of the compounds the sensitizing properties of the cyanine dyes are predicted. The reflection spectrum of Gs2-9 coated in photographic emulsions showed J-aggregation behaviour at λ = 560 nm. Unsymmetric benzimidazole-indole cyanine dyes showed good to excellent green sensitizing properties in photographic emulsions, whereas symmetric indole cyanine dyes showed heavy residual colour and no sensitizing properties.

COLORING COMPOSITION, COLORING COMPOSITION FOR COLOR FILTER, AND COLOR FILTER

-

, (2018/02/28)

PROBLEM TO BE SOLVED: To provide a coloring composition using a salt-forming compound, which is soluble in a solvent and can be used as a bright red dye, a coloring composition for a color filter, which is excellent in brightness, heat resistance, and a contrast ratio when used for a color filter, and a color filter having no generation of foreign substances on a coating film. SOLUTION: The coloring composition comprises a salt-forming compound of a cationic cyanine dye represented by general formula (1-1), and an organic solvent. In the formula, A1 and A2 each independently represent -CR12(R13)- or -S-; R1 to R11 each independently represent H, a substituted or unsubstituted alkyl group or the like; R12 and R13 each independently represent a substituted or unsubstituted alkyl group or the like; and Anion- represents a specific sulfate anion. COPYRIGHT: (C)2015,JPO&INPIT

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