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194785-18-7

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  • 1H,5H,11H,15H-Xantheno[2,3,4-ij:5,6,7-i'j']diquinolizin-18-ium,9-(2,5-dicarboxyphenyl)-2,3,6,7,12,13,16,17-octahydro-, inner salt/ LIDE PHARMA- Factory supply / Best price

    Cas No: 194785-18-7

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  • 1H,5H,11H,15H-Xantheno[2,3,4-ij:5,6,7-i'j']diquinolizin-18-ium,9-(2,5-dicarboxyphenyl)-2,3,6,7,12,13,16,17-octahydro-, inner salt

    Cas No: 194785-18-7

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194785-18-7 Usage

Uses

Different sources of media describe the Uses of 194785-18-7 differently. You can refer to the following data:
1. 6-Carboxy-X-rhodamine is a single isomer, long wavelength rhodamine dye.
2. 6-Carboxy-X-rhodamine is a rhodamine based dye for use in tracer agents, laser dyes, labeling agents for biologics, etc.

Check Digit Verification of cas no

The CAS Registry Mumber 194785-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,7,8 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 194785-18:
(8*1)+(7*9)+(6*4)+(5*7)+(4*8)+(3*5)+(2*1)+(1*8)=187
187 % 10 = 7
So 194785-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C33H30N2O5/c36-32(37)20-9-10-21(33(38)39)24(17-20)27-25-15-18-5-1-11-34-13-3-7-22(28(18)34)30(25)40-31-23-8-4-14-35-12-2-6-19(29(23)35)16-26(27)31/h9-10,15-17H,1-8,11-14H2,(H-,36,37,38,39)

194785-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Carboxy-X-rhodamine

1.2 Other means of identification

Product number -
Other names 6-ROX [6-Carboxy-X-Rhodamine]

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:194785-18-7 SDS

194785-18-7Downstream Products

194785-18-7Relevant articles and documents

Preparation process of carboxyl-X-rhodamine

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Paragraph 0069-0070, (2022/03/27)

The invention provides a preparation process of carboxyl-X-rhodamine, which adopts 8-hydroxyjulolidine phenol and trimellitic anhydride as raw materials, an intermediate 5, 6-carboxyl-X-rhodamine is synthesized by a direct cyclization method, a high-boiling-point solvent is adopted as a cyclization medium, and a cyclization product has poor solubility in the solvent and can be precipitated in a reaction system, so that the yield of 5, 6-carboxyl-X-rhodamine is increased, and the yield of 5, 6-carboxyl-X-rhodamine is increased. Therefore, the reaction conversion rate and the purification simplicity are obviously improved; 5, 6-carboxyl-X-rhodamine and organic amine are salified, so that the separation cost is greatly reduced, the operation steps are simplified, and the industrial production of carboxyl-X-rhodamine becomes possible; an acid precipitation method is adopted, the 5-carboxyl-X-rhodamine ammonium salt and the 6-carboxyl-X-rhodamine ammonium salt are converted into the 5-carboxyl-X-rhodamine and the 6-carboxyl-X-rhodamine, and the efficiency is high; the whole preparation process has the advantages of simplicity and convenience in operation, low equipment requirement, low cost, high equipment use efficiency and the like, and meets the requirements of industrial production and application.

Compounds and Method for Imaging Cancer

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, (2018/10/21)

A compound, a method of imaging a cell, and a method of detecting a cancer, an inflammatory disease, or a neoplastic disease are provided. The compound includes a nitroxide derivative of a fluorophore that is activatable upon exposure to free radicals. The method of imaging a cell includes contacting the cell with an activatable nitroxide derivative of a fluorophore. The method of detecting a cancer, an inflammatory disease, or a neoplastic disease includes administering an activatable nitroxide derivative of a fluorophore and then imaging one or more cells contacted with the compound.

METHODS FOR SYNTHESIZING RHODAMINE DYES

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Paragraph 0101, (2017/05/17)

Described herein are methods for the regioselective synthesis of substituted rhodamine dyes.

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