IP Library Granted Patent US 8,813,675
Granted Patent B2
US 8,813,675 · App. 13/945,397 · Granted Aug 26, 2014

Time-temperature indicators comprising crystallized diacetylenic indicator compounds

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Quick Facts
Patent No.
US 8,813,675
App. No.
13/945,397
Granted
Aug 26, 2014
Kind
B2
Abstract

Crystallized diacetylenic compounds having certain crystallographic and other characteristics; diacetylenic compounds and mixtures crystallized from diacetylenic solutions; methods of preparing and identifying solvent systems for dissolving diacetylenic compounds; diacetylenic solutions; methods of recrystallizing diacetylenic compounds; crystals of 2,4-hexadiyn-1,6-bis(alkylurea) compounds; and ambient condition indicators and time-temperature condition indicators comprising crystallized diacetylenic compounds.

Claims (28)

1. A time-temperature indicator comprising:

a crystallized diacetylenic compound capable of polymerizing in the solid state to provide an irreversible appearance change in an environmental condition indicator; and

a substrate onto which the crystallized diacetylenic compound is applied;

wherein a change in appearance of the crystallized diacetylenic compound is detectable in a manner that is useful to indicate a time-temperature condition;

wherein the crystallized diacetylenic compound is symmetrically substituted and having the structural formula:

R 3 NHCONH—R 4 —C≡C═C≡C—R 4 —NHCONHR 3

wherein R 4 is methylene, ethylene, propylene or butylene, R 3 is ethyl or propyl, the crystallized diacetylenic compound having a crystal structure wherein the crystallized diacetylenic compound molecules have a center-to-center separation, referring to the geometric centers of diacetylene units in adjacent molecules, of less than 4.7 Å, the center-to-center separation being in a direction wherein solid-state polymerization can occur.

2. The time-temperature indicator of claim 1 wherein the center-to-center separation corresponds to a unit cell repeat distance of the crystallized diacetylenic compound.

3. The time-temperature indicator of claim 1 , wherein the crystallized diacetylenic compound comprises two hydrogen bonds for each NHCONH urea group, each one of the two hydrogen bonds extending between one of the two NH groups in a urea group in one polymerizable diacetylenic molecule and a C═O group in an adjacent polymerizable diacetylenic molecule.

4. The time-temperature indicator of claim 1 , wherein the crystallized diacetylenic compound has a triclinic crystal structure including a center of symmetry wherein no axes or planes of symmetry exist.

5. The time-temperature indicator of claim 1 , wherein the crystallized diacetylenic compound has a monoclinic crystal structure.

6. The time-temperature indicator of claim 1 , wherein the crystallized diacetylenic compound has a purity of at least about 99 percent by weight.

7. The time-temperature indicator of claim 1 comprising at least one non-acetylenic compound in a crystal phase of the diacetylenic compound.

8. A time-temperature indicator comprising a crystallized diacetylenic compound according to claim 1 wherein the crystallized diacetylenic compound is 2,4-hexadiyn-1,6-bis(ethylurea).

9. A time-temperature indicator comprising a crystallized diacetylenic compound according to claim 1 wherein the crystallized diacetylenic compound is 2,4-hexadiyn-1,6-bis(propylurea).

10. A time-temperature indicator comprising a solid phase composition including a crystallized diacetylenic compound disposed on a substrate; wherein a change in appearance of the crystallized diacetylenic compound is detectable; having the structural formula

R 3 NHCONH—R 4 —C≡C—C≡C—R 4 —NHCONHR 3

wherein R 4 is methylene, ethylene, propylene or butylene, R 3 is ethyl or propyl; and

the solid phase comprises a triclinic space group P-1;

the crystallized diacetylenic compound being capable of polymerizing to provide a color change in response to ambient heat and comprising two hydrogen bonds for each NHCONH urea group, each one of the two hydrogen bonds extending between one of the two NH groups in a urea group in one polymerizable diacetylenic molecule and a C═O group in an adjacent polymerizable diacetylenic molecule.

11. A time-temperature indicator comprising a solid phase composition including a crystallized diacetylenic compound and a substrate, wherein the crystallized diacetylenic compound has the structural formula

R 3 NHCONH—R 4 —C≡C—C≡C—R 4 —NHCONHR 3

wherein R 4 is methylene, ethylene, propylene or butylene, R 3 is ethyl or propyl; and

the solid phase comprises a monoclinic space group P2 1/a or space group P2 1/c wherein, in each space group, the b axis is the 2 1 axis;

the crystallized diacetylenic compound molecule being capable of polymerizing to provide a color change in response to ambient heat and comprising two hydrogen bonds for each NHCONH urea group, each one of the two hydrogen bonds extending between one of the two NH groups in a urea group in one polymerizable diacetylenic molecule and a C═O group in an adjacent polymerizable diacetylenic molecule.

12. The time temperature indicator of claim 1 , wherein the crystallized diacetylenic compound is crystallized from a mixture of water and ethanol.

13. The time temperature indicator of claim 10 , wherein the crystallized diacetylenic compound is crystallized from a mixture of 25% water in ethanol.

14. The time temperature indicator of claim 10 , wherein the crystallized diacetylenic compound is crystallized from a mixture of water and ethanol.

Assignments (9)
MERGER Recorded May 29, 2025
From: TEMPTIME CORPORATION
To: ZEBRA TECHNOLOGIES CORPORATION
Reel/Frame 071548/0054 →
RELEASE OF SECURITY INTEREST - 364 - DAY Recorded Mar 5, 2021
From: JPMORGAN CHASE BANK, N.A.
To: ZEBRA TECHNOLOGIES CORPORATION; LASER BAND, LLC; TEMPTIME CORPORATION
Reel/Frame 056036/0590 →
SECURITY INTEREST Recorded Sep 1, 2020
From: ZEBRA TECHNOLOGIES CORPORATION; LASER BAND, LLC; TEMPTIME CORPORATION
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053841/0212 →
SECURITY INTEREST Recorded Apr 25, 2019
From: TEMPTIME CORPORATION
To: JPMORGAN CHASE BANK, N.A, AS COLLATERAL AGENT
Reel/Frame 048995/0241 →
RELEASE OF SECURITY AGREEMENT Recorded Feb 28, 2019
From: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
To: TEMPTIME CORPORATON
Reel/Frame 048462/0325 →
RELEASE OF SECURITY INTEREST Recorded Feb 28, 2019
From: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
To: TEMPTIME CORPORATION
Reel/Frame 048462/0163 →
SECURITY INTEREST Recorded Dec 11, 2014
From: TEMPTIME CORPORATION
To: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
Reel/Frame 034483/0143 →
SECURITY AGREEMENT Recorded Sep 13, 2013
From: TEMPTIME CORPORATION
To: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
Reel/Frame 031265/0599 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2013
From: BAUGHMAN, RAY H.; HALL, LEE J.; KOZLOV, MIKHAIL; SMITH, DAWN E.; PRUSIK, THADDEUS
To: TEMPTIME CORPORATION
Reel/Frame 031061/0095 →