CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE
  • CAS No.:555-60-2
Other grades of this product :
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Basic information
Product Name:CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE
Synonyms:(3-CHLOROPHENYL)HYDRAZONOMALONONITRILE;MESOXALONITRILE 3-CHLOROPHENYLHYDRAZONE;CCCP;[(3-chlorophenyl)hydrazono]-propanedinitril;m-chlorophenylcarbonylcyanidehydrazone;mesoxalonitrile,(m-chlorophenyl)hydrazone;M-CL-CCP;MESOXALONITRILE (3-CHLOROPHENYL)HYDRAZONE;BUTTPARK 91\04-41;CARBONYL CYANIDE M-CHLOROPHENYL-HYDRAZONE
CAS:555-60-2
MF:C9H5ClN4
MW:204.62
EINECS:209-103-7
Product Categories:Caspases/Apoptosis
Mol File:555-60-2.mol
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Chemical Properties
Melting point 170-175 °C (dec.)
Boiling point 333.84°C (rough estimate)
density 1.3807 (rough estimate)
refractive index 1.6110 (estimate)
storage temp. -20°C
solubility methanol: 10 mg/mL, clear, very deep yellow
form powder
pka6.00±0.10(Predicted)
color yellow to orange
Water Solubility Insoluble in water. Soluble in DMSO (5 mg/ml), ethanol (1 mg/ml) and methanol (10 mg/ml).
BRN 1842102
Exposure limitsNIOSH: IDLH 25 mg/m3
InChIKeyUGTJLJZQQFGTJD-UHFFFAOYSA-N
CAS DataBase Reference555-60-2(CAS DataBase Reference)
EPA Substance Registry SystemPropanedinitrile, [(3-chlorophenyl)hydrazono]- (555-60-2)
Safety Information
Hazard Codes T
Risk Statements 23/24/25-36/37/38
Safety Statements 26-36/37-45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS FG5600000
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29280090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Usage And Synthesis
DescriptionCCCP is a protonophore mitochondrial uncoupler that increases membrane permeability to protons, leading to a disruption in the mitochondrial membrane potential. It inhibits mitochondrial respiration and ATPase activity when used at concentrations of 110 and 35 nM, respectively. CCCP inhibits activation of stimulation of interferon genes (STING), decreasing the expression of downstream STING targets, including IFN-β, TBK1, and IRF3 when used at a concentration of 50 μM in RAW 264.7 cells. It induces mitochondrial fission in a manner dependent on the GTPase Drp1. CCCP (4 mg/kg) increases body temperature as well as left ventricular systolic and diastolic dimensions and decreases fractional shortening in rats. It also increases myocardial glucose and fatty acid uptake in rats.
Chemical Propertiesyellow to orange-brown crystalline powder
UsesCarbonyl cyanide 3-chlorophenylhydrazone is a widely used uncoupler of oxidative phosphorylation.
UsesCarbonyl cyanide 3-chlorophenylhydrazone (CCCP) has been used:
  • in the inhibition of efflux pump in clinical Pseudomonas aeruginosa
  • to inhibit oxidative phosphorylation activity of mitochondria in human Beas-2B bronchial epithelial cells
  • to prepare carbonyl cyanide m-chlorophenylhydrazone solution for oxidative and mitochondrial stress assay and mitophagy induction in Caenorhabditis elegans
Biological ActivityWidely used uncoupler of oxidative phosphorylation.
Biochem/physiol ActionsCarbonyl cyanide 3-chlorophenylhydrazone (CCCP) induces mitophagy in mammalian cells. CCCP suppresses the expression of few electron transport chain (ETC) proteins. Protonophore (H+ ionophore) and uncoupler of oxidative phosphorylation in mitochondria. Shown to have a number of effects on cellular calcium. Inhibits secretion of hepatic lipase and partially inhibits the pH gradient-activated Cl- uptake and Cl-/Cl- exchange activities in brush-border membrane vesicles.
in vitroa genetic β-galactoside reporter system with a disk diffusion assay on macconkey lactose agar petri plates to monitor maintenance of the bacteriophage λ prophage state and viral induction in escherichia coli k-12. it presented evidence that the phage λ major lytic promoters, pl and pr, are activated via cells containing the reporters following exposure to the energy poison cccp. requirement of expression of the λ lytic promoters in response to cccp is host reca function and an auto-cleavable ci repressor, as does sos induction of the λ prophage occurring by a dna damage-dependent pathway. cccp-mediated activation of the λ lytic promoters required λ cro function. cccp does not modulate an sfi-lacz sos reporter [1]. the uncoupler cccp blocks oxidative phosphorylation by damaging the proton gradient. an anion cccp can bind a proton. but cccp with a delocalized negative charge allows it to cross the lipid bilayer in the unprotonated form, while weak acids cross the hydrophobic membrane only when protonated. many protons can be transported by one molecule of cccp across the inner membrane. it is described that a genetic reporter system to monitor maintenance of the λ prophage state and viral induction, and evidence is presented that it activates the major leftward and rightward lytic promoters of the λ prophage that cells are exposed to the energy poison cccp.
references[1]. thomason lc, court dl. evidence that bacteriophage λ lysogens may induce in response to the proton motive force uncoupler cccp. fems microbiol lett. 2016 feb;363(3).
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Preparation Products And Raw materials

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