Abstract: A method of reducing malodor on surfaces including providing an apparatus in an environment including a surface wherein the surface has a malodor containing compound selected from: amine-containing compound and thiol-containing compound. The apparatus includes a volatile material having a volatile carbonyl containing compound. The volatile material is exposed to the environment such that the volatile carbonyl containing compound vaporises and deposits on the surface. The carbonyl containing compound undergoes a nucleophilic addition in the presence of the malodor containing compound.

Abstract: Provided herein are methods, chemical library and simulation system for performing in situ patterned chemistry. Methods, systems and assays comprising the use of the synthesized chemical libraries, which increase explored protein space in a knowledge-based manner, are also provided for characterizing antibody-target interactions including: identifying target proteins of antibodies, characterizing antibody-binding regions in target proteins, identifying linear and structural epitopes in target proteins, and determining the propensity of antibody binding to target proteins.

Abstract: Provided herein are molecules and salts thereof, arrays containing molecules and salts thereof, solid supports containing molecules and salts thereof, kits containing molecules or salts thereof, and methods of determining alignment of photolithographic masks comprising molecules or salts thereof.

Abstract: Methods, computer systems, and computer storage media are provided that enables clinicians to create and interact with snapshots of critical clinical/non-clinical information that is readily accessible in future visits. Initially, an indication to create a key note corresponding to a clinical note of a patient encounter for a patient is received. A selection of a key note section that will be associated with the key note is also received. Upon the clinical note being signed, the key note is created and saved. Upon receiving a request from a user, a key note window is provided in a user interface. The user interface enables the user to expand a header corresponding to a particular key note to display details associated with the corresponding encounter. A hyperlink to original summary notes from which the particular key note was created may be provided by the user interface.

Abstract: Molecules or salts thereof are provided, having the structure in Formula I, wherein n2 and n4 are the same or different and are independently 1, 2, or 3, and n3 is 1 to 20; X is oxygen, nitrogen, or sulfur; wherein R1, R2, R3, R4, R5, R6, and R7 are as described herein. Methods are also provided for the synthesis of and use of the provided molecules in applications for diagnostic testing.

Abstract: Provided herein are molecules and salts thereof, arrays containing molecules and salts thereof, solid supports containing molecules and salts thereof, kits containing molecules or salts thereof, and methods of determining alignment of photolithographic masks comprising molecules or salts thereof.

Abstract: Molecules or salts thereof are provided, having the structure in Formula I, wherein n2 and n4 are the same or different and are independently 1, 2, or 3, and n3 is 1 to 20; X is oxygen, nitrogen, or sulfur; wherein R1, R2, R3, R4, R5, R6, and R7 are as described herein. Methods are also provided for the synthesis of and use of the provided molecules in applications for diagnostic testing.

Abstract: The gel compositions as described herein, are less affected by changes in humidity, are readily formed into complex shapes, and can contain high loadings of the hydrophobic material, even when the material is not highly hydrophobic, and provide a more controlled release of the hydrophobic material.

Abstract: A volatile composition having: (i) greater than 30% of a scented hydrophobic material by weight of the volatile composition, wherein the scented hydrophobic material comprises one or more volatile compounds; and (ii) greater than 20% of a regulating scent intensity (RIS) composition by weight of the volatile composition. The RIS composition has at least two of: a first regulating scent intensity component (RIS component) having a high average vapor pressure (VP); a second RIS component having a medium average VP; and a third RIS component having a low average VP; The average VP of each of said one or more volatile compounds is lower than at least one of the high, medium and low average VPs of the first, second and third RIS components at the same temperature.

Abstract: A scent intensity regulating composition (RIS composition). The RIS composition includes at least two of: a first scent intensity regulating component (RIS component) having an average vapor pressure (VP) greater than 0.3 Torr at 25° C.; a second RIS component having an average VP from 0.07 to 0.3 Torr at 25° C.; and a third RIS component having an average VP from 0.0099 to 0.07 Torr at 25° C. Each of the first, second, and third RIS components is characterized by an Odor Detection Threshold (ODT) of greater than 20 ppb.

Abstract: The gel compositions as described herein, are less affected by changes in humidity, are readily formed into complex shapes, and can contain high loadings of the hydrophobic material, even when the material is not highly hydrophobic, and provide a more controlled release of the hydrophobic material. It is believed that the slow release is achieved by forming the gel to have a tight cross-linked network with small pore-size. The pore size is correlated to the average correlation length as measured using Small Angle X-Ray Scattering (SAXS). By limiting the average correlation length to less than 8 nm, preferably from 0.3 nm to 8 nm, more preferably from 0.3 nm to 4 nm, a long lasting release of the hydrophobic material is achieved, rather than a blooming effect, whereby the hydrophobic material is released in a short burst.

Abstract: Methods, computer systems, and computer storage media are provided that enables clinicians to create and interact with snapshots of critical clinical/non-clinical information that is readily accessible in future visits. Initially, an indication to create a key note corresponding to a clinical note of a patient encounter for a patient is received. A selection of a key note section that will be associated with the key note is also received. Upon the clinical note being signed, the key note is created and saved. Upon receiving a request from a user, a key note window is provided in a user interface. The user interface enables the user to expand a header corresponding to a particular key note to display details associated with the corresponding encounter. A hyperlink to original summary notes from which the particular key note was created may be provided by the user interface.

Abstract: An antibacterial air freshening product for an interior environment. The product includes a container containing 1 ml to 50 ml of a freshening composition in fluid communication with a membrane. The composition is substantially free of a surfactant and has from 0.5% to 20% of a volatile aldehyde mixture, by weight of the composition. The volatile aldehyde mixture includes a C5 to C8 unbranched unsubstituted linear alkenal and a C9 to C14 unbranched unsubstituted linear alkenal. A weight ratio of the C5 to C8 unbranched unsubstituted linear alkenal to the C9 to C14 unbranched unsubstituted linear alkenal is from 3:1 to 1:3.

Abstract: Molecules compounds are provided having the structure in Formula I, or a salt thereof, wherein n1 is independently 0, 1, 2, or 3; n2 is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20; n3 is from 0, 1, 2, or 3; n4 is 0 or 1; and n5 is 0, 1, 2, or 3; and wherein X is O, N, or S; Y, Z, XX, and YY are the same or different and are independently O or S; ZZ comprises nitrogen, oxygen, sulfur, or selenium; and wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12 are as described herein. Methods are also provided for the synthesis of and use of the provided molecules in applications for diagnostic testing.

Abstract: Molecules or salts thereof are provided, having the structure in Formula I, wherein n2 and n are the same or different and are independently 1, 2, or 3, and n is 1 to 20; X is oxygen, nitrogen, or sulfur; wherein R1, R2, R3, R4, R5, R6, and R7 are as described herein. Methods are also provided for the synthesis of and use of the provided molecules in applications for diagnostic testing.

Abstract: A method of reducing malodor on surfaces including providing an apparatus in an environment including a surface wherein the surface has a malodor containing compound selected from: amine-containing compound and thiol-containing compound. The apparatus includes a volatile material having a volatile carbonyl containing compound. The volatile material is exposed to the environment such that the volatile carbonyl containing compound vaporises and deposits on the surface. The carbonyl containing compound undergoes a nucleophilic addition in the presence of the malodor containing compound.

Abstract: Provided herein are methods, chemical library and simulation system for performing in situ patterned chemistry. Methods, systems and assays comprising the use of the synthesized chemical libraries, which increase explored protein space in a knowledge-based manner, are also provided for characterizing antibody-target interactions including: identifying target proteins of antibodies, characterizing antibody-binding regions in target proteins, identifying linear and structural epitopes in target proteins, and determining the propensity of antibody binding to target proteins.

Abstract: The gel compositions as described herein, are less affected by changes in humidity, are readily formed into complex shapes, and can contain high loadings of the hydrophobic material, even when the material is not highly hydrophobic, and provide a more controlled release of the hydrophobic material.

Abstract: The gel compositions as described herein, are less affected by changes in humidity, are readily formed into complex shapes, and can contain high loadings of the hydrophobic material, even when the material is not highly hydrophobic, and provide a more controlled release of the hydrophobic material. It is believed that the slow release is achieved by forming the gel to have a tight cross-linked network with small pore-size. The pore size is correlated to the average correlation length as measured using Small Angle X-Ray Scattering (SAXS). By limiting the average correlation length to less than 8 nm, preferably from 0.3 nm to 8 nm, more preferably from 0.3 nm to 4 nm, a long lasting release of the hydrophobic material is achieved, rather than a blooming effect, whereby the hydrophobic material is released in a short burst.

Abstract: Provided herein are molecules and salts thereof, arrays containing molecules and salts thereof, solid supports containing molecules and salts thereof, kits containing molecules or salts thereof, and methods of determining alignment of photolithographic masks comprising molecules or salts thereof.