2,4,6-Triiodophenol

Names

[ CAS No. ]:
609-23-4

[ Name ]:
2,4,6-Triiodophenol

[Synonym ]:
2,6-Triiodophenol
2,4,6-Triiodophenol
Phenol,4,6-triiodo
2,4,6-Trijodfenol
triiodo-2,4,6 phenol
2,3-DIHYDROXYL QUINOXALINE
Phenol, 2,4,6-triiodo-
Phenol,2,4,6-triiodo
EINECS 210-186-7
2,4,6-Trijodfenol [Czech]
2,4,6-triIPhOH
MFCD00002179
2,4,6-triiodo-phenol

Biological Activity

[Description]:

2,4,6-Triiodophenol is an orally active and potent leukotriene B4 (LTB4) synthesis inhibitor. 2,4,6-Triiodophenol can induce mouse blastocysts apoptosis[1][2].

[Related Catalog]:

Signaling Pathways >> Apoptosis >> Apoptosis

Research Areas >> Others

[In Vitro]

2,4,6-Triiodophenol (5-50 μM; 0-100 h) impairs the quality of pre-implantation mouse embryos in a dose-dependent manner, inducing decline of both total and trophectoderm cell numbers[2]. 2,4,6-Triiodophenol (5 μM; 85 h) shows increasement of apoptotic cells in mouse pre-implantation embryos[2]. 2,4,6-Triiodophenol (5-50 μM; 100 h) induces oxidative stress in mouse pre-implantation embryos[2]. Apoptosis Analysis[2] Cell Line: Mouse blastocyst cells Concentration: 5 μM Incubation Time: 85 hours Result: Showed signals of activated Caspase-3/7. Immunofluorescence[2] Cell Line: Mouse blastocyst cells Concentration: 5-50 μM Incubation Time: 100 hours Result: Resulted in marked increase of oxygen species (ROS) treated with high dose of 2,4,6-Triiodophenol.

Chemical & Physical Properties

[ Density]:
3.1±0.1 g/cm3

[ Boiling Point ]:
316.3±42.0 °C at 760 mmHg

[ Melting Point ]:
157-159 °C(lit.)

[ Molecular Formula ]:
C₆H₃I₃O

[ Molecular Weight ]:
471.801

[ Flash Point ]:
145.1±27.9 °C

[ Exact Mass ]:
471.731781

[ PSA ]:
20.23000

[ LogP ]:
3.88

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.816

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: SN2800000

CHEMICAL NAME :: Phenol, 2,4,6-triiodo-

CAS REGISTRY NUMBER :: 609-23-4

BEILSTEIN REFERENCE NO. :: 2046861

LAST UPDATED :: 199701

DATA ITEMS CITED :: 3

MOLECULAR FORMULA :: C6-H3-I3-O

MOLECULAR WEIGHT :: 471.79

WISWESSER LINE NOTATION :: QR BI DI FI

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: >4 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: PHARAT Pharmazie. (VEB Verlag Volk und Gesundheit, Neue Gruenstr. 18, Berlin DDR-1020, Ger. Dem. Rep.) V.1- 1946- Volume(issue)/page/year: 18,642,1963

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 180 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#03493

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
SN2800000

[ HS Code ]:
2908199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2908199090

[ Summary ]:
HS: 2908199090. derivatives of polyphenols or phenol-alcohols containing only halogen substituents and their salts. VAT:17.0%. tax rebate rate:9.0%. supervision conditions:None. MFN tariff:5.5%. general tariff:30.0%

Articles

Distribution of dehalogenation activity in subseafloor sediments of the Nankai Trough subduction zone.

Philos. Trans. R. Soc. Lond., B, Biol. Sci. 368(1616) , 20120249, (2013)

Halogenated organic matter buried in marine subsurface sediment may serve as a source of electron acceptors for anaerobic respiration of subseafloor microbes. Detection of a diverse array of reductive...

Comparative developmental toxicity of new aromatic halogenated DBPs in a chlorinated saline sewage effluent to the marine polychaete Platynereis dumerilii.

Environ. Sci. Technol. 47(19) , 10868-76, (2013)

Using seawater for toilet flushing may introduce high levels of bromide and iodide into a city's sewage treatment works, and result in the formation of brominated and iodinated disinfection byproducts...

Fast speciation analysis of iodophenol compounds in river waters by capillary electrophoresis-inductively coupled plasma-mass spectrometry with off-line solid-phase microextraction.

Electrophoresis 25(12) , 1843-51, (2004)

An analytical methodology for the fast separation and determination of iodophenol species in natural water samples was developed using capillary electrophoresis (CE) coupled to inductively coupled pla...

Related Compounds

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