p-Phenylene diisothiocyanate

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
1,4-Diisothiocyanatobenzene, Bitoscanate, PDITC
Nonfluorochemicals
KUMI0F350
4044-65-9
MFCD00004811
19958
2414340
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Melting Point
Packaging
Storage
p-Phenylene diisothiocyanate
C8H4N2S2
192.26
≥98%
White to Beige Solid
129-131°C
5g,10g,20g,50g,100g,500g,1kg and 25kg
Store at 2-8°C temp.
p-Phenylene diisothiocyanate (also named as 1,4-Diisothiocyanatobenzene, Bitoscanate, PDITC) was previously used as an organic chemical in the treatment of hookworms. Recently, it has been extended in various applications in organic synthesis.
A ratiometric fluorescent chemosensor for Hg2+ based on FRET and its application in living cells. [1]
Rational design and synthesis of polythioureas as capacitor dielectrics. [2]
New tris(hydroxypyridinone) bifunctional chelators containing isothiocyanate groups provide a versatile platform for rapid one-step labeling and PET imaging with 68Ga3+. [3]
Multifunctional Desferrichrome Analogues as Versatile 89Zr (IV) Chelators for ImmunoPET Probe Development. [4]
Design, synthesis and evaluation of novel bifunctional tetrahydroxamate chelators for PET imaging of 89Zr-labeled antibodies. [5]
References:
[1] C.Wang, et al, Sensor Actuat. B-Chem., 2014, 198(31), pp 33-40.
[2] R.Ma, et al, J. Mater. Chem. A, 2015, 3(28), pp 14845-14852.
[3] M.T.Ma, et al, Bioconjugate Chem., 2016, 27(2), pp 309-318.
[4] C.J.Adams, et al, Mol. Pharm., 2017, 14(8), pp 2831-2842.
[5] J.Rousseau, et al, Bioorg. Med. Chem. Lett., 2017, 27(4), pp 708-712.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Danger
H301,H315,H319,H334,H335
P261,P301+P310,P305+P351+P338,P342+P311
2930909899
UN 2811 6.1/PG III

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