44:
793:
toxicological properties of this compound have not been investigated, so all health effects are unknown. To best prevent bodily harm or injury it is recommended that all direct contact be avoided and the compound be kept under extremely strict environmentally controlled conditions. In case of spillage it is recommended that a local fire department be called in advance prior to any attempt at cleaning. In case of fire it is recommended that the material be left to burn and the surrounding area be evacuated. If fire fighting is required it is recommended that a fully positive pressure
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35:
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The primary hazard of working with 2,4,6-trinitrobenzenesulfonic acid is the risk of instantaneous explosion. 2,4,6-Trinitrobenzenesulfonic acid is an extremely sensitive compound especially when mixed with other compounds, exposed to heat, or exposed to rapid temperature or pressure changes. The
760:
even in the presence of water or organic solvents because of the explosive tendencies of aromatic nitro compounds which increase in the presence of multiple nitro groups. Not much is known about this compound, but it is used as a peptide terminal amino group neutralizer and is currently being
820:"Treatment of Experimental (Trinitrobenzene Sulfonic Acid) Colitis by Intranasal Administration of Transforming Growth Factor (Tgf)-β1 Plasmid: TGF-β1–Mediated Suppression of T Helper Cell Type 1 Response Occurs by Interleukin (Il)-10 Induction and IL-12 Receptor β2 Chain Downregulation"
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883:
Antoniou, Efstathios; Margonis, Georgios
Antonios; Angelou, Anastasios; Pikouli, Anastasia; Argiri, Paraskevi; Karavokyros, Ioannis; Papalois, Apostolos; Pikoulis, Emmanouil (2016-08-19).
769:
Its primary usage is primarily to neutralize peptide terminal amino groups in scientific research. Occasionally it is used as a detonator for certain other explosive compounds.
559:
692:
614:
752:, it may begin a vigorous reaction that culminates in almost immediate detonation. The aromatic nitro compounds may explode in the presence of a base such as
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Atsushi Kitani; Ivan J. Fuss; Kazuhiko
Nakamura; Owen M. Schwartz; Takashi Usui; Warren Strober (2000).
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InChI=1S/C6H3N3O9S/c10-7(11)3-1-4(8(12)13)6(19(16,17)18)5(2-3)9(14)15/h1-2H,(H,16,17,18)
148:
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819:
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InChI=1/C6H3N3O9S/c10-7(11)3-1-4(8(12)13)6(19(16,17)18)5(2-3)9(14)15/h1-2H,(H,16,17,18)
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740:. Due to its extreme oxidative properties, if mixed with reducing agents including
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Except where otherwise noted, data are given for materials in their
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in the colon of laboratory animals in order to model
885:"The TNBS-induced colitis animal model: An overview"
70:
Picrylsulfonic acid; Trinitrobenzene sulfonate; TNBS
761:investigated for its effects on the immune system.
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8:
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26:
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788:Health concerns and safety precautions
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352:Key: NHJVRSWLHSJWIN-UHFFFAOYSA-N
167:
147:
61:2,4,6-Trinitrobenzene-1-sulfonic acid
7:
824:The Journal of Experimental Medicine
797:be used along with either foam or CO
28:2,4,6-Trinitrobenzene Sulfonic Acid
871:Comparative Toxicogenomics Database
362:Key: NHJVRSWLHSJWIN-UHFFFAOYAG
252:
795:self-contained breathing apparatus
383:O=S(=O)(O)c1c(cc(cc1()=O)()=O)()=O
25:
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416:
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42:
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673:(at 25 °C , 100 kPa).
889:Annals of Medicine and Surgery
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1:
867:Trinitrobenzenesulfonic Acid
712:Trinitrobenzenesulfonic acid
18:Trinitrobenzenesulfonic acid
1002:
901:10.1016/j.amsu.2016.07.019
778:inflammatory bowel disease
772:It is also used to induce
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41:
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976:Nitrobenzene derivatives
782:irritable bowel syndrome
534:Precautionary statements
609:
981:Benzenesulfonic acids
608:
836:10.1084/jem.192.1.41
780:and post-infectious
591:(fire diamond)
57:Preferred IUPAC name
971:Explosive chemicals
758:potassium hydroxide
443: g·mol
129:Beilstein Reference
29:
700:Infobox references
647:Related compounds
610:
27:
986:Liquid explosives
954:, cameochemicals.
708:Chemical compound
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705:
653:Related compounds
516:Hazard statements
305:CompTox Dashboard
117:Interactive image
16:(Redirected from
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201:ECHA InfoCard
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169:ChEMBL3586251
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830:(1): 41–52.
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76:Identifiers
68:Other names
658:Picric acid
502:Signal word
453:0.955 g/cm
392:Properties
207:100.017.925
149:CHEBI:53063
965:Categories
805:References
476:Pictograms
436:Molar mass
283:8T3HQG2ZC4
180:ChemSpider
104:3D model (
83:CAS Number
909:2049-0801
735:oxidizing
732:nitroaryl
572:P342+P311
568:P333+P313
560:P304+P341
556:P302+P352
467:labelling
294:UN number
228:219-717-7
220:EC Number
93:2508-19-2
927:27656280
895:: 9–15.
854:10880525
750:nitrides
746:sulfides
742:hydrides
730:S) is a
588:NFPA 704
458:Hazards
243:1051138
918:5021709
845:1887715
774:colitis
693:what is
691: (
449:Density
250:PubChem
134:572358
952:savety
925:
915:
907:
852:
842:
748:, and
688:verify
685:
508:Danger
441:293.16
376:SMILES
160:ChEMBL
51:Names
341:InChI
298:0386
263:11045
189:10577
140:ChEBI
106:JSmol
940:MSDS
923:PMID
905:ISSN
850:PMID
765:Uses
738:acid
580:P501
576:P363
564:P321
552:P285
548:P280
544:P272
540:P261
526:H334
522:H317
274:UNII
913:PMC
897:doi
840:PMC
832:doi
828:192
756:or
465:GHS
310:EPA
253:CID
967::
921:.
911:.
903:.
893:11
891:.
887:.
869:,
848:.
838:.
826:.
822:.
784:.
744:,
714:(C
636:OX
578:,
574:,
570:,
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550:,
546:,
542:,
524:,
469::
929:.
899::
873:.
856:.
834::
799:2
728:9
726:O
724:3
722:N
720:3
718:H
716:6
683:N
629:4
622:4
615:2
429:S
426:9
423:O
420:3
417:N
414:3
411:H
408:6
405:C
312:)
308:(
108:)
20:)
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