ChemicalBook > CAS DataBase List > CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE

Product Name
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE
CAS No.
555-60-2
Chemical Name
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE
Synonyms
CCCP;Carbonyl Cyanide;(3-CHLOROPHENYL)HYDRAZONOMALONONITRILE;MESOXALONITRILE 3-CHLOROPHENYLHYDRAZONE;CCCP;CCCPH;M-CL-CCP;m-Cl-CCP (CCCP);BUTTPARK 91\04-41;TIMTEC-BB SBB003506;CCCP apoptosis inducer;3-chlorophenylhydrazone
CBNumber
CB0421559
Molecular Formula
C9H5ClN4
Formula Weight
204.62
MOL File
555-60-2.mol
More
Less

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Property

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
pka
6.00±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 limits
NIOSH: IDLH 25 mg/m3
InChIKey
UGTJLJZQQFGTJD-UHFFFAOYSA-N
CAS DataBase Reference
555-60-2(CAS DataBase Reference)
EPA Substance Registry System
Propanedinitrile, [(3-chlorophenyl)hydrazono]- (555-60-2)
More
Less

Safety

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
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C2759
Product name
Carbonyl cyanide 3-chlorophenylhydrazone
Purity
≥97% (TLC), powder
Packaging
1g
Price
$176
Updated
2024/03/01
Sigma-Aldrich
Product number
215911
Product name
Carbonyl Cyanide
Packaging
250mg
Price
$130
Updated
2024/03/01
Alfa Aesar
Product number
L06932
Product name
Carbonyl cyanide 3-chlorophenylhydrazone, 98%
Packaging
100mg
Price
$25.4
Updated
2024/03/01
Alfa Aesar
Product number
L06932
Product name
Carbonyl cyanide 3-chlorophenylhydrazone, 98%
Packaging
500mg
Price
$67.3
Updated
2024/03/01
Cayman Chemical
Product number
25458
Product name
CCCP
Purity
≥98%
Packaging
100mg
Price
$32
Updated
2024/03/01
More
Less

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Chemical Properties,Usage,Production

Description

CCCP 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 Properties

yellow to orange-brown crystalline powder

Uses

Carbonyl cyanide 3-chlorophenylhydrazone is a widely used uncoupler of oxidative phosphorylation.

Uses

Carbonyl 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

Definition

ChEBI: CCCP is a member of the class of monochlorobenzenes that is benzene substituted by 2-(1,3-dinitrilopropan-2-ylidene)hydrazinyl and chloro groups at positions 1 and 3, respectively. It is a mitochondrial depolarizing agent that induces reactive oxygen species mediated cell death. It has a role as a geroprotector, an antibacterial agent and an ionophore. It is a nitrile, a hydrazone and a member of monochlorobenzenes. It is functionally related to a hydrazonomalononitrile.

Biological Activity

Widely used uncoupler of oxidative phosphorylation.

Biochem/physiol Actions

Carbonyl 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 vitro

a 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.

storage

Store at RT

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

Raw materials

Preparation Products

More
Less

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE Suppliers

ATK CHEMICAL COMPANY LIMITED
Tel
3429815786 13301662590
Fax
+86-21-51619052
Email
sales@atkchemical.com
Country
China
ProdList
10006
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7583
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
Advantage
57
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11714
Advantage
57
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4647
Advantage
58
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
ShangHai Caerulum Pharma Discovery Co., Ltd.
Tel
18149758185
Email
sales-cpd@caerulumpharma.com
Country
China
ProdList
3421
Advantage
58
Shanghai Meishui Chemical Technology Co., Ltd
Tel
021-60549325 18616193163
Fax
021-33250306
Country
China
ProdList
4528
Advantage
56
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Shanghai CanSpecsci Instrument Co., Ltd.
Tel
400-6087598 15021221957
Fax
4006087598-8012
Email
order@canspecsci.com
Country
China
ProdList
2071
Advantage
56
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Fax
+86-21-52996696
Country
China
ProdList
4121
Advantage
55
Chengdu Chuangkecheng Biological Technology Co., Ltd.
Tel
028-028-0000000 13008177686
Fax
15928581901
Email
sales@ckcbiotech.com
Country
China
ProdList
736
Advantage
55
Shanghai Qiao Chemical Science Co., Ltd
Tel
021-58892003
Email
info@qiaochem.com
Country
China
ProdList
5881
Advantage
65
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
27322
Advantage
60
ShangHai Biochempartner Co.,Ltd
Tel
17754423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8011
Advantage
62
Beijing Solarbio Science & Tecnology Co., Ltd.
Tel
010-50973130 4009686088
Email
3193328036@qq.com
Country
China
ProdList
29797
Advantage
68
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19806
Advantage
60
Wuxi AppTec
Tel
022-59987777 13552403979
Email
jia_guoqiang@wuxiapptec.com
Country
China
ProdList
22346
Advantage
58
Aikon International Limited
Tel
025-66028182 18112977050
Fax
(3)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
15820
Advantage
58
Rhawn Reagent
Tel
400-400-1332688 18019345275
Fax
400-133-2688
Email
amy@rhawn.cn
Country
China
ProdList
15503
Advantage
58
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400-6387771-6038 18902104717
Email
sales@heowns.com
Country
China
ProdList
20512
Advantage
60
UHN Shanghai Research & Development Co., Ltd.
Tel
021-58958002 18930822973
Fax
021-58958618
Email
xiaoyangw@gmail.com
Country
China
ProdList
2129
Advantage
58
Henan Alfachem Co.,Ltd.
Tel
0371-0371-55051623 18137891487
Fax
QQ:2853979817
Email
2853979817@qq.com
Country
China
ProdList
9968
Advantage
58
Angel Pharmatech, Ltd.
Tel
17317130613
Fax
QQ3358272972
Email
3358272972@qq.com
Country
China
ProdList
3238
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
400-400-400-9004166 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52712
Advantage
58
Beijing OKA biological technology co., LTD
Tel
010-62971590 18548936886
Fax
010-62340519
Email
3462612863@qq.com
Country
China
ProdList
6912
Advantage
58
Hefei Bomei Biotechnology Co., Ltd.
Tel
13739298932
Email
531626407@qq.com
Country
China
ProdList
2999
Advantage
58
DC Chemicals
Tel
021-58447131 13564518121
Email
sales@dcchemicals.com
Country
China
ProdList
9414
Advantage
58
Changzhou Chenhong Biotechnology Co., Ltd.
Tel
0519-85788828 13775037613
Email
sales@chemrenpharm.com
Country
China
ProdList
3553
Advantage
58
Chengdu Peter-like Biotechnology Co., Ltd.
Tel
028-81700200 18108052721
Email
2850505130@qq.com
Country
China
ProdList
5182
Advantage
58
Chongqing Chemdad Co., Ltd
Tel
+86-023-61398051 +8613650506873
Email
sales@chemdad.com
Country
China
ProdList
39916
Advantage
58
Absin Bioscience Inc.
Tel
021-38015121 15000105423
Email
chenjw@absin.cn
Country
China
ProdList
24734
Advantage
58
Shanghai hongqu biomedical technology co. LTD
Tel
88888888888
Email
hongquchem@qq.com
Country
China
ProdList
5132
Advantage
58
ShangHai ChuanQian Chemcial Technique Centre
Tel
15869524721
Email
3525679403@qq.com
Country
China
ProdList
3864
Advantage
58
MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8141
Advantage
58
NORANA GROUP
Tel
027-027-59209883 17386169806
Fax
027-59209883
Email
service@nornachem.com
Country
China
ProdList
4604
Advantage
58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.
Tel
021-51816796-820 13611835272
Fax
021-5161 3951
Email
sales2@sunwaypharm.com
Country
China
ProdList
44490
Advantage
58
More
Less

View Lastest Price from CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE 555-60-2
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-11
Career Henan Chemical Co
Product
CCCP 555-60-2
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200kg
Release date
2018-12-25

555-60-2, CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONERelated Search:


  • (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
  • CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZONE
  • CCCP
  • 3-chlorophenylhydrazone
  • [(3-CHLOROPHENYL)HYDRAZONO]PROPANEDINITRILE
  • [(3-chlorophenyl)hydrazono]malononitrile
  • CARBONYL CYANIDE M-CHLOROPHENYL &
  • Carbonylcyanide3-chlorophenylhydrazone,98%
  • Carbonyl cyanide 3-chlorophenylhydrazone, 99+%
  • Carbonylcyanid-m-chlorphenylhydrazon
  • m-Cl-CCP, Carbonyl cyanide 3-chlorophenylhydrazone, CCCP, Mesoxalonitrile (3-chlorophenyl)hydrazone, Mesoxalonitrile 3-chlorophenylhydrazone
  • m-Cl-CCP, CCCP, Mesoxalonitrile 3-chlorophenylhydrazone
  • Carbonyl cyanide m-chlorophenylhydrazone, 99+%
  • 2-[(3-Chlorophenyl)hydrazono]propanedinitrile
  • CCCPH
  • Carbonyl cyanide 3-chlorophenylhydrazone,m-Cl-CCP, CCCP, Mesoxalonitrile 3-chlorophenylhydrazone
  • (3-chlorophenyl)carbonohydrazonoyl dicyanide
  • Carbonyl Cyanide
  • TIMTEC-BB SBB003506
  • ((3-chlorophenyl)hydrazono)-propanedinitril
  • Carbonyl Cyanide m-Chlorophenylhydrazone - CAS 555-60-2 - Calbiochem
  • Propanedinitrile, 2-[2-(3-chlorophenyl)hydrazinylidene]-
  • 2-[2-(3-Chlorophenyl)hydrazinylidene]propanedinitrile
  • CCCP apoptosis inducer
  • m-Cl-CCP (CCCP)
  • 2-[(3-chlorophenyl)hydrazinylidene]propanedinitrile
  • N-(3-chlorophenyl)carbonohydrazonoyldicyanide
  • CCCP,Mesoxalonitrile 3-chlorophenylhydrazone
  • 555-60-2
  • C9H5ClN4
  • C9H5CIN4
  • ClC6H4NHNCCN2
  • Organic Covalent Modifiers
  • Enzyme Inhibitors
  • Enzymes, Inhibitors, and Substrates
  • Enzyme Inhibitors by Type
  • BioChemical
  • Biochemicals and Reagents
  • Caspases/Apoptosis