IP Library Granted Patent US 9,791,369
Granted Patent B2
US 9,791,369 · App. 14/003,957 · Granted Oct 17, 2017

Visualization kit comprising a fluorescent agent and a cyanoacrylate, and method of cofumigation of a fluorescent agent and a cyanoacrylate

Inventors: Cosimo Prete (Villeneuve D'ascq, FR); Pierre Audebert (Cachan, FR); Laurent Galmiche (Cachan, FR); Clemence Allain (Cachan, FR)
Assignees: CRIME SCIENCE TECHNOLOGY; ECOLE NORMALE SUPERIEURE DE CACHAN; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE—CNRS
G01N21/64C07D257/08C07D403/04A61B5/1172
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 9,791,369
App. No.
14/003,957
Granted
Oct 17, 2017
Kind
B2
Abstract

A visualization kit includes (i) a cyanoacrylate and (ii) a fluorescent agent containing at least one tetrazine of formula 1: wherein X and Y represent independently a nonionic, electron-withdrawing group selected from halogens, azide, cyano and O-A-R, in which A represents a single bond or a C1-C4 alkyldiyl and R is alkyl, alkenyl, alkynyl, cycloalkyl or epoxyalkyl, or an aziridine group, which is optionally substituted by alkyl or aryl. A method of cofugation and a method of visualizing traces on a substrate utilizing these components are also presented.

Claims (37)

1. A visualization kit comprising:

(A) a cyanoacrylate; and

(B) a fluorescent agent comprising at least one tetrazine of formula 1:

wherein X and Y represent independently

a nonionic, electron-withdrawing group selected from halogens, azide, cyano and O-A-R, in which A represents a single bond or a C1-C4 alkyldiyl and R is alkyl, alkenyl, alkynyl, cycloalkyl or epoxyalkyl; or

an aziridine group, which is optionally substituted by alkyl or aryl.

2. The kit according to claim 1 , wherein the fluorescent agent has a molecular weight of less than 400 g·mol −1 , a sublimation temperature of less than 200° C., and an extinction coefficient of less than 2950 L·mol −1 ·cm −1 .

3. The kit of claim 1 , wherein the fluorescent agent has a brightness of more than 200 L·mol −1 ·cm −1 .

4. The kit of claim 1 , wherein X and Y are selected independently from the group consisting of halogens, azide, cyano and —OR in which R is alkyl, alkenyl, alkynyl, cycloalkyl, and epoxyalkyl.

5. The kit of claim 1 , wherein the at least one tetrazine of formula 1 is selected from the group consisting of 3,6-dichloro-1,2,4,5-tetrazine, 3-chloro-6-methoxy-1,2,4,5-tetrazine, 3-chloro-6-ethoxy-1,2,4,5-tetrazine, 3,6-dimethoxy-1,2,4,5-tetrazine, 3-chloro-6-(prop-2-enyloxy)-1,2,4,5-tetrazine, 3-chloro-6-(prop-2-ynyloxy)-1,2,4,5-tetrazine, 3-chloro-6-(adamant-2-yloxy)-1,2,4,5-tetrazine, 3-chloro-6-(adamant-1-ylmethoxy)-1,2,4,5-tetrazine, 3-chloro-6-(3-epoxybutyloxy)-1,2,4,5-tetrazine, the product of formula

and mixtures thereof.

6. The kit of claim 1 , wherein the cyanoacrylate is a cyanoacrylate of formula 2:

in which R 1 is alkyl, alkenyl, alkynyl, cycloalkyl or aryl, and R 1 may be optionally substituted by a halogen or a hydroxyl group.

7. The kit of claim 1 , wherein the cyanoacrylate is selected from the group consisting of methyl 2-cyanoacrylate, ethyl 2-cyanoacrylate, propyl 2-cyanoacrylate, butyl 2-cyanoacrylate, allyl 2-cyanoacrylate, methoxyethyl 2-cyanoacrylate, ethoxyethyl 2-cyanoacrylate, 2-chloroethyl 2-cyanoacrylate, cyclohexyl 2-cyanoacrylate, ethoxycarbonylmethyl 2-cyanoacrylate, trifluoroethyl 2-cyanoacrylate and mixtures thereof.

8. A composition, comprising

(A) a cyanoacrylate, and

(B) a fluorescent agent comprising at least one tetrazine of formula 1:

wherein X and Y represent independently

a nonionic, electron-withdrawing group selected from halogens, azide, cyano and O-A-R in which A represents a single bond or a C1-C4 alkyldiyl and R is alkyl, alkenyl, alkynyl, cycloalkyl or epoxyalkyl; or

an aziridine group, which is optionally substituted by alkyl or aryl.

9. A method, comprising cofumigation of

(A) a cyanoacrylate, and

(B) a fluorescent agent comprising at least one tetrazine of formula 1:

wherein X and Y represent independently

a nonionic, electron-withdrawing group selected from halogens, azide, cyano and O-A-R in which A represents a single bond or a C1-C4 alkyldiyl and R is alkyl, alkenyl, alkynyl, cycloalkyl or epoxyalkyl; or

an aziridine group, which is optionally substituted by alkyl or aryl.

10. The method of claim 9 , wherein the ratio by weight between the amount of the cyanoacrylate and the amount of the fluorescent agent is from 100:1 to 500:1.

11. The method of claim 9 , wherein the ratio by weight between the amount of the cyanoacrylate and the amount of the fluorescent agent is from 100:1 to 200:1.

12. The method of claim 9 , wherein the cofumigation is carried out at a temperature between 80° C. and 120° C.

13. A method for visualizing traces on a substrate, comprising the steps of:

presenting said substrate bearing traces to a device comprising means of fumigation and containing (A) a cyanoacrylate and (B) a fluorescent agent comprising at least one tetrazine of formula 1:

wherein X and Y represent independently

a nonionic, electron-withdrawing group selected from halogens, azide, cyano and O-A-R in which A represents a single bond or a C1-C4 alkyldiyl and R is alkyl, alkenyl, alkynyl, cycloalkyl or epoxyalkyl; or

an aziridine group, which is optionally substituted by alkyl or aryl;

cofumigating the compounds (A) and (B) by the method as defined in claim 9 with the aid of said device, to give a fumigated substrate; and

submitting said fumigated substrate to ultraviolet light.

14. A method of using the visualization kit of claim 1 for the visualization of traces on a substrate, said method comprising cofumigating the cyanoacrylate and the fluorescent agent in the presence of a substrate bearing traces.

Assignments (2)
CHANGE OF NAME Recorded Sep 13, 2017
From: CRIME SCENE TECHNOLOGY
To: CRIME SCIENCE TECHNOLOGY
Reel/Frame 043572/0805 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2014
From: PRETE, COSIMO; AUDEBERT, PIERRE; GALMICHE, LAURENT; ALLAIN, CLEMENCE
To: CRIME SCENE TECHNOLOGY; ECOLE NORMALE SUPERIEURE DE CACHAN; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS
Reel/Frame 032579/0353 →
Priority Claims (1)
FR 11 51828 · Mar 7, 2011 · national
Continuity (1)
Related Publication 20140004620A1 · Jan 2, 2014