IP Library › Granted Patent US 9,012,688
Granted Patent B2
US 9,012,688 · App. 13/571,763 · Granted Apr 21, 2015

Fluorescent material for self-erasable writing, authentic security labeling, currency counterfeit prevention and processes for the preparation thereof

Inventors: Ajayaghosh Ayyappanpillai (Kerala, IN); Thirumalai Kumaran Rajasekaran (Kerala, IN)
Assignee: Council of Scientific and Industrial Research
C09D11/50C09D11/17
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,012,688
App. No.
13/571,763
Granted
Apr 21, 2015
Kind
B2
Abstract

The present invention provides a novel fluorescent molecule having formula 1 which exhibit emission color change when in contact with moisture useful for the preparation of fluorescent paper, allowing self-erasable writing, security label for document authenticity, check and prevention of currency counterfeit. Compound of formula 1, when coated on paper, results in blue emitting surfaces on which writing is possible using water as ink. The images undergo self-erasal after 6 hours making the paper reusable or instantly with hot air. The images are visible only on illumination with a UV lamp having wavelength 365 nm. The material can be coated on any document to create security label which changes color on touching with a wet surface or water pen and will go back to the native color when the moisture is dried off after a time frame.

Claims (8)

1. Compound of general formula 1

2. The compound of formula 1 as claimed in claim 1 , wherein said compound is useful as fluorescent material for self-erasable writing, authentic security labeling, currency counterfeit prevention.

3. A process for the preparation of compound of general formula 1 comprising the steps of:

i. refluxing compound 3 with compound 2 in tetrahydrofuran and triethylamine in the ratio ranging between 1:1 to 1:1.5 in the presence of catalyst at temperature in the range of 55 to 65° C. for period in the range of 11 to 13 h under argon atmosphere;

ii. cooling the reaction mixture as obtained in step (i) at temperature in the range of 25 to 30° C. followed by extracting using chloroform to obtain combined organic layer;

iii. washing the combined organic layer as obtained in step (ii) with water, brine followed by drying over anhydrous sodium sulphate and purifying using column chromatography with 10% methanol-chloroform as eluent to obtain compound of general formula 1

4. The process as claimed in claim 3 , wherein catalyst used in step (i) are 5 to 10 mol % Bis(triphenylphosphine)palladium(II) chloride [PdCl 2 (PPh 3 ) 2 ] and 5 to 10 mol % Copper iodide (CuI).

5. The process as claimed in claim 3 , wherein yield of the compound of general formula 1 is in the range of 72-75%.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2013
From: AYYAPPANPILLAI, AJAYAGHOSH; RAJASEKARAN, THIRUMALAI KUMARAN
To: COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH
Reel/Frame 029712/0178 →
Priority Claims (1)
IN 2294/DEL/2011 · Aug 12, 2011 · national
Continuity (1)
Related Publication 20130209665A1 · Aug 15, 2013