Product Name :
2,6-TDI (CAS 91-08-7)
Synonym :
Application :
CAS:
91-08-7
Purity:
Molecular Weight:
174.16
Formula :
C9H6N2O2
Physical state:
Liquid
solubility :
Shipping Condition :
Store at 4° C
Melting point:
20-22° C
SMILES:
CC1=C(C=CC=C1N=C=O)N=C=O
References:
:A comparative respiratory sensitization study of 2,4- and 2,6-toluene diisocyanate using guinea pigs. | Shiotsuka, RN., et al. 2000. Inhal Toxicol. 12: 605-15. PMID: 10880147Exposure to 2,4- and 2,6-toluene diisocyanate (TDI) during production of flexible foam: determination of airborne TDI and urinary 2,4- and 2,6-toluenediamine (TDA). (S)-1-(4-Bromopheny)ethylamine Order | Kääriä, K., et al. 2001. Analyst. 126: 1025-31. DABCO-Bis(sulfur dioxide) Price PMID: 11478630Development, validation and characterization of an analytical method for the quantification of hydrolysable urinary metabolites and plasma protein adducts of 2,4- and 2,6-toluene diisocyanate, 1,5-naphthalene diisocyanate and 4,4′-methylenediphenyl diisocyanate. | Sennbro, CJ., et al. 2003. Biomarkers. 8: 204-17. PMID: 12944173Improvement in the GC-MS method for determining urinary toluene-diamine and its application to the biological monitoring of workers exposed to toluene-diisocyanate. | Sakai, T., et al. 2005. Int Arch Occup Environ Health. 78: 459-66. PMID: 15918038Biological monitoring of isocyanates and related amines. IV. 2,4- and 2,6-toluenediamine in hydrolysed plasma and urine after test-chamber exposure of humans to 2,4- and 2,6-toluene diisocyanate. | Brorson, T., et al. 1991. Int Arch Occup Environ Health. 63: 253-9. PMID: 1660449The GSTP1 Ile105 Val polymorphism modifies the metabolism of toluene di-isocyanate. | Broberg, KE., et al. 2010. Pharmacogenet Genomics. 20: 104-11. PMID: 20032816Biological monitoring as a valid tool to assess occupational exposure to mixtures of 2,4-:2,6-toluene diisocyanate. | De Palma, G., et al. 2012. Med Lav. 103: 361-71. PMID: 23077796Development of a method for quantification of toluene diisocyanate and methylenediphenyl diisocyanate migration from polyurethane foam sample surface to artificial sweat by HPLC-UV-MS. | Donchenko, A., et al. 2020. J Chromatogr B Analyt Technol Biomed Life Sci. 1142: 122027. PMID: 32145637An Ab Initio Investigation on Relevant Oligomerization Reactions of Toluene Diisocyanate (TDI). | Thangaraj, R., et al. 2022. Polymers (Basel). 14: PMID: 36236129Determination of toluenediamine isomers by capillary gas chromatography and chemical ionization mass spectrometry with special reference to the biological monitoring of 2,4- and 2,6-toluene diisocyanate. | Skarping, G., et al. 1994. J Chromatogr A. 663: 199-210. PMID: 8173666Toxicokinetics of 2,4- and 2,6-toluenediamine in hydrolysed urine and plasma after occupational exposure to 2,4- and 2,6- toluene diisocyanate. | Lind, P., et al. 1996. Occup Environ Med. 53: 94-9. PMID: 8777457Formation, solvolysis, and transcarbamoylation reactions of bis(S-glutathionyl) adducts of 2,4- and 2,6-diisocyanatotoluene. | Day, BW., et al. 1997. Chem Res Toxicol. 10: 424-31. PMID: 9114980Albumin adducts in plasma from workers exposed to toluene diisocyanate. | Lind, P., et al. 1997. Analyst. 122: 151-4. PMID: 9124697
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