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1 linkage, which provide identification of the diisocyanate.
2 subsequently cross-linked with hexamethylene diisocyanate.
3 ted a strong positive reaction to isophorone diisocyanate.
4 d low molecular weight diols and unsymmetric diisocyanates.
5 ts a novel route to fully renewable aromatic diisocyanates.
6  by a strong positive reaction to isophorone diisocyanate, 1.0%, in petrolatum.
7 thesis reaction with 4,4'-methylene diphenyl diisocyanate (4,4'-MDI) circumvents harsh reaction condi
8 onamide (PTSA), (iii) 4,4'-methylenediphenyl diisocyanate (4,4'-MDI), (iv) toluenediisocyanate (TDI),
9                             Treatment of the diisocyanate 43 with 2 equiv of the iminophosphorane 7 f
10 nd skin proteins that become conjugated with diisocyanate after in vitro and in vivo exposure.
11 rate gram-scale preparation of 1,4-phenylene diisocyanate and 2,5-toluene diisocyanate and formulatio
12 by condensation polymerization between hexyl-diisocyanate and Boc-protected serinol in the presence o
13 f 1,4-phenylene diisocyanate and 2,5-toluene diisocyanate and formulation of these monomers to prepar
14                        Mixing of equal molar diisocyanate and hindered diamine leads to formation of
15 cromolecular alcohols with excess isophorone diisocyanate and subsequent derivatization of the isocya
16 t were used in polymerizations with aromatic diisocyanates and short chain diols.
17                                              Diisocyanates are asthma-causing chemicals used in the c
18                                              Diisocyanates are considered as skin and respiratory sen
19                                              Diisocyanates are highly reactive chemical compounds wid
20                                              Diisocyanates are the leading cause of occupational asth
21 boxylic acid azo-calix[4]arene using toluene diisocyanate as a linker and characterized by FT-IR, TGA
22  against the clinical visit rates identified diisocyanates as the strongest predictor of AD.
23 ntly associated with a clinical diagnosis of diisocyanate asthma (DA).
24 n (56-kD) differed from the predominant lung diisocyanate-conjugated keratin (47-kD).
25 to liquid-phase HDI, although the major skin diisocyanate-conjugated protein (56-kD) differed from th
26 samples, whereas albumin was the predominant diisocyanate-conjugated protein in bronchoalveolar lavag
27 in 18 was also identified as the predominant diisocyanate-conjugated protein in human endobronchial b
28 Keratin was also identified as a predominant diisocyanate-conjugated protein in human skin biopsy sam
29 nase, and actin were identified as prominent diisocyanate-conjugated proteins through use of a combin
30         Introducing an oil-soluble polymeric diisocyanate cross-linker into the oil phase prior to ho
31                                    Moreover, diisocyanate cross-linking at the oil/water interface le
32                                              Diisocyanates disrupted the production of beneficial lip
33 o be an important step in the development of diisocyanate (dNCO)-specific allergic sensitization; how
34           Urinary diamines are biomarkers of diisocyanate exposure.
35 h cross-linking of iohexol and hexamethylene diisocyanate followed by coprecipitation of the resultin
36 ute to renewable terephthalates and aromatic diisocyanates from D-galactose via Eastwood olefination
37  this work, gamma-cyclodextrin-hexamethylene diisocyanate (gamma-CD-HDI), gamma-cyclodextrin-epichlor
38                                     Although diisocyanates have been identified as causative agents o
39 ins can become conjugated with hexamethylene diisocyanate (HDI) and may be biologically important in
40     The isocyanate monomer 1,6-hexamethylene diisocyanate (HDI) and one of its trimers, HDI isocyanur
41 on test (DLST) for isocyanate (hexamethylene diisocyanate [HDI]) reagent was positive in blood and th
42 hyde (MDA), glutaraldehyde and hexamethylene diisocyanate (HMDC).
43                  We previously reported that diisocyanate-human serum albumin (DIISO-HSA) stimulated
44 nking, diisocyanate self-polymerization, and diisocyanate hydrolysis.
45 on of poly(ethylene glycol) to hexamethylene diisocyanate in solution has been performed.
46 d other proteins as potential "carriers" for diisocyanates in vivo, and suggest that HDI conjugation
47 teins may play a role in the pathogenesis of diisocyanate-induced asthma.
48 e (HDI) and may be biologically important in diisocyanate-induced asthma.
49                                     Aromatic diisocyanates, invaluable commodity chemicals for polyme
50 tafluoro-1,6-hexanediol (16F) and isophorone diisocyanate (IPDI).
51 cal improvements that differed by study site diisocyanate levels.
52                 Oligomer ions containing the diisocyanate linkage are also observed in the spectrum,
53  observation of oligomer ions containing the diisocyanate linkage, which provide identification of th
54 ustrial intermediate 4,4'-methylene diphenyl diisocyanate (MDI) is thought to be an important step in
55 ustrial MDA mixtures, and methylene diphenyl diisocyanate (MDI) mixtures used in polyurethane synthes
56 ltimeric MDA species, and methylene diphenyl diisocyanate (MDI) mixtures.
57     MDA is a precursor to methylene diphenyl diisocyanate (MDI), a hard block component in polyuretha
58                              Diphenylmethane diisocyanate (MDI), the chemical commonly used as a cros
59 ally important isomers, 2,4- and 2,6-toluene diisocyanate, on human serum albumin at varying diisocya
60      Preparation of these renewable aromatic diisocyanates proceeds without the use of high-pressure
61                                              Diisocyanate-protein conjugation results in a variety of
62                               At a low (1:2) diisocyanate/protein ratio, five binding sites are ident
63 socyanate, on human serum albumin at varying diisocyanate/protein ratios.
64 nderstand the chemical species produced when diisocyanates react with protein, tandem mass spectromet
65 ding intra- and intermolecular crosslinking, diisocyanate self-polymerization, and diisocyanate hydro
66                                   Therefore, diisocyanates show temporospatial and epidemiological as
67                          Exposure to toluene diisocyanate (TDI), an industrially important crosslinki
68     Inhalation of irritants, such as toluene diisocyanate (TDI), stimulates substance P (SP) release
69 p and characterize a murine model of toluene diisocyanate (TDI)-induced rhinitis.
70 GP) molecules are reacted with hexamethylene diisocyanate trimer (HDI) and polyethylene glycol (PEG)
71 ctrum, providing a means for identifying the diisocyanate used for PUR syntheses.
72 alates, which were transformed into aromatic diisocyanates via Curtius rearrangement in flow.
73 ized from poly(vinyl alcohol) and isophorone diisocyanate was performed by covalent attachment to fre
74 ment of exposure to the most common aromatic diisocyanates within targeted groups as well as larger p