IP Library Granted Patent US 11,318,083
Granted Patent B2
US 11,318,083 · App. 16/812,700 · Granted May 3, 2022

Compositions and methods for reshaping keratin-rich substrates and forming adherent flexible films

Inventors: Barry C. Arkles (Pipersville, PA); Jonathan D. Goff (Philadelphia, PA); Alison Ane Phillips (Feasterville, PA); Kerry Campbell Demella (Philadelphia, PA)
Assignee: GELEST, INC.
A61K8/892A61K8/362A61K8/41A61K8/585A61Q5/002A61Q5/06
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Quick Facts
Patent No.
US 11,318,083
App. No.
16/812,700
Granted
May 3, 2022
Kind
B2
Abstract

Compositions and methods for reshaping keratin-rich substrates while forming adherent flexible films contain emulsified or soluble mixtures of silanols and hemiaminals or the reaction products of silanols and hemiaminals including silylated hemiaminals. A method for treating split-ends in hair is also described.

Claims (16)

1. A method for relaxing and reshaping a keratin-rich substrate comprising:

(a) applying a substrate-activating composition to the substrate;

(b) warming and drying the substrate;

(c) applying a fixative composition to the substrate; and

(d) warming and drying the substrate;

wherein the fixative composition comprises a silylated hemiaminal which is formed in situ by the reaction of at least one silanol and at least one organic hemiaminal in the presence of at least one siloxane without formation formaldehyde; and

wherein the substrate-activating component is an aqueous solution having a pH of about 1 to 4 or a pH of about 10 to 13.

2. The method according to claim 1 , wherein steps (b) and (c) are performed simultaneously.

3. The method according to claim 1 , wherein the at least one organic hemiaminal is a linear hemiaminal ether.

4. The method according to claim 1 , wherein the at least one organic hemiaminal is selected from the group consisting of a hemiaminal silyl ether and a hemiacetal silyl ether.

5. The method according to claim 1 , wherein the at least one organic hemiaminal is selected from the group consisting of imidazolidinyl urea, diazolidinyl urea, and polyoxymethylene urea.

6. The method according to claim 1 , wherein the at least one silanol is a monomeric, polymeric, or resinous organosilanol.

7. The method according to claim 1 , wherein the at least one silanol is a hydroxy-terminated polymeric diorganosiloxane.

8. The method according to claim 1 , wherein the at least one silanol is an organosilanetriol or diorganosilanediol.

9. The method according to claim 1 , wherein the fixative composition further comprises an amine bound to a polymeric siloxane.

10. The method according to claim 1 , wherein the fixative composition comprises an organosilanetriol and a diorganosiloxane.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2024
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 068467/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2022
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 058668/0350 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2021
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 058595/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2021
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 056272/0183 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2020
From: ARKLES, BARRY C., PHD; GOFF, JONATHAN D.; PHILLIPS, ALISON ANE; DEMELLA, KERRY CAMPBELL
To: GELEST TECHNOLOGIES, INC.
Reel/Frame 052053/0420 →
Continuity (2)
Provisional Application 62838691 · Apr 25, 2019
Related Publication 20200337983A1 · Oct 29, 2020