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Ammonium 1-pyrrolidinedithiocarbamate

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Ammonium 1-pyrrolidinedithiocarbamate manufacturers

Ammonium 1-pyrrolidinedithiocarbamate Basic information
Product Name:Ammonium 1-pyrrolidinedithiocarbamate
Synonyms:1-Pyrrolidinecarbodithioic acid, ammonium salt,95%;Ammonium Pyrrolidine-N-dithiocarba;PDTC Pyrrolidinedithiocarbamate, ammonium derivative;Ammonium pyrrolidinedithiocarbamate,1-Pyrrolidinecarbodithioic acid ammonium salt, APDC, Ammonium pyrrolidinecarbodithioate, PDC, PDTC;Ammonium pyrrolidine;1-Pyrrolidinecarbodithioic acid, aMMoniuM salt, 98% 25GR;Ammonium Pyrrolidine-N-dithiocarbamate 1-Pyrrolidinecarbodithioic Acid Ammonium Salt Pyrrolidine-N-dithiocarbamic Acid Ammonium Salt;PYRROLIDINE-1-DITHIOCARBOXYLIC ACID AMMO
CAS:5108-96-3
MF:C5H9NS2.H3N
MW:164.3
EINECS:225-834-4
Product Categories:Nitric Oxide;5108-96-3
Mol File:5108-96-3.mol
Ammonium 1-pyrrolidinedithiocarbamate Structure
Ammonium 1-pyrrolidinedithiocarbamate Chemical Properties
Melting point 153-155 °C(lit.)
density 1.117 (estimate)
bulk density400kg/m3
refractive index 1.5300 (estimate)
storage temp. Store at +2°C to +8°C.
solubility 190g/l
form Powder/Solid
color White to off-white
PH6-7 (50g/l, H2O, 20℃)
biological sourcemicrobial
Water Solubility 50 g/L (20 ºC)
Sensitive Hygroscopic
BRN 3730472
Stability:Stable. Incompatible with strong oxidizing agents.
InChI1S/C5H9NS2.H3N/c7-5(8)6-3-1-2-4-6;/h1-4H2,(H,7,8);1H3
InChIKeyMDDIUTVUBYEEEM-UHFFFAOYSA-N
SMILESN.SC(=S)N1CCCC1
CAS DataBase Reference5108-96-3(CAS DataBase Reference)
EPA Substance Registry System1-Pyrrolidinecarbodithioic acid, ammonium salt (5108-96-3)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36-37/39
WGK Germany 3
F 3
TSCA TSCA listed
HS Code 29339990
Storage Class11 - Combustible Solids
MSDS Information
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Ammonium 1-pyrrolidinedithiocarbamate Usage And Synthesis
DescriptionPyrrolidinedithiocarbamic acid (PDTC) is a metal chelating compound that potently and reversibly inhibits NF-κB activation in vitro (100 μM). At 300 μM, it prevents TNF-α gene expression and protein production in human monocytes after LPS application. In vascular smooth muscle cells, PDTC (10 μM) arrests the cell cycle at the G1 phase with upregulation of p21Cip1 through the p38 MAPK pathway. PDTC (100 μM) also has antioxidant properties.
Chemical Propertiespale yellow crystalline solid
UsesAmmonium pyrrolidinedithiocarbamate has been used:
  • to inhibit nuclear factor κB (NF-κB) mobilization and TNF (tumor necrosis factor) production in human monocytes
  • to reduce neutrophil activity in rats
  • to prevent Ca2+ influx in adriamycin (ADR)-treated podocytes

to abrogate the microRNA-146a promoter luciferase reporter activity in human brain cells
Uses1-Pyrrolidinecarbodithioic Acid induces apoptosis in rat smooth muscle cells and inhibits apoptosis in leukemia HL-60 cells. It also prevents induction of nitric oxide synthetase by inhibiting translation of NOS mRNA;
General DescriptionAmmonium pyrrolidinedithiocarbamate is a nuclear factor κB (NF-κB) inhibitor. It functions as a chelating agent, which allows the preconcentration of trace metals from solution. Pyrrolidinedithiocarbamate (PDTC) has antioxidant properties. It inhibits apoptosis in lymphocytes, neurons and vascular endothelial cells.
Biochem/physiol ActionsPrevents induction of nitric oxide synthetase by inhibiting translation of NOS mRNA; induces apoptosis in rat smooth muscle cells and inhibits apoptosis in leukemia HL-60 cells.
Purification MethodsPurify the salt by recrystallising twice by dissolving in MeOH and adding Et2O. It has also been purified by recrystallisation from EtOH. It is used for the precipitation of As, Bi, Cd, Co, Cu, Fe, Mn, Ni, Pb, Sb, Su, V and Zn from acidic solutions [Kinrade & van Loon Anal Chem 46 1894 1974]. The ethyl ester has b 87-89o/0.01mm. [Synthesis and Polarography: Kitagawa & Taku Bull Chem Soc Jpn 64 2151 1973, Malissa & Sch.ffmann Mikrochim Acta 187 1955, Beilstein 20 III/IV 195, 20/1 V 331.]
References[1] R SCHRECK. Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells.[J]. Journal of Experimental Medicine, 1992, 175 5: 1181-1194. DOI: 10.1084/jem.175.5.1181
[2] H. ZIEGLER-HEITBROCK. Pyrrolidine dithiocarbamate inhibits NF-kappa B mobilization and TNF production in human monocytes.[J]. Journal of immunology, 1993, 151 12 1: 6986-6993. DOI: 10.4049/jimmunol.151.12.6986
[3] SUNG-KWON MOON. PDTC, metal chelating compound, induces G1 phase cell cycle arrest in vascular smooth muscle cells through inducing p21Cip1 expression: Involvement of p38 mitogen activated protein kinase[J]. Journal of Cellular Physiology, 2003, 198 2: 310-323. DOI: 10.1002/jcp.10728
[4] SUOWEN XU . Tanshinone II-A inhibits oxidized LDL-induced LOX-1 expression in macrophages by reducing intracellular superoxide radical generation and NF-κB activation[J]. Translational Research, 2012, 160 2: Pages 114-124. DOI: 10.1016/j.trsl.2012.01.008
Ammonium 1-pyrrolidinedithiocarbamate Preparation Products And Raw materials
Tag:Ammonium 1-pyrrolidinedithiocarbamate(5108-96-3) Related Product Information
Ammonium acetate Ammonium formate Phenyl chlorothionocarbonate N-Methyl-2-pyrrolidone Ammonium chloride Ammonium sulfate Polyvinylpyrrolidone Ammonium hydroxide 5-Pyrazolecarboxylic acid Thiobenzoic acid Ammonium nitrate AMMONIUM Ammonium dithiocarbamate AMMONIUM CARBAMATE Ammonium 1-pyrrolidinedithiocarbamate 2-Oxo-2-(3-oxotetrahydro-1H-pyrazol-1-yl)ethyl 1-pyrrolidinecarbodithioate (3-Chloro-5-(trifluoromethyl)(2-pyridylthio))pyrrolidinylmethane-1-thione (2,6-Dichloro-4-pyridyl)methyl pyrrolidine-1-carbodithioate