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1825-21-4

1825-21-4 Structure

1825-21-4 Structure
IdentificationBack Directory
[Name]

PENTACHLOROANISOLE
[CAS]

1825-21-4
[Synonyms]

NCI-C56520
Pentachloroani
PENTACHLORANISOLE
PCP, Methyl ether
PENTACHLOROANISOLE
FivechloroMethyl ether
methylpentachlorophenate
pentachloromethoxy-benzen
Pentachloromethoxybenzene
Methyl pentachlorophenate
2,3,4,5,6-PENTACHLOROANISOLE
2,3,4,5,6-pentachloro-anisol
Benzene, pentachloromethoxy-
pentachlorophenylmethylether
methylpentachlorophenylester
methylpentachlorophenylether
Pentachloroanisole (100μg/mL)
PENTACHLOROANISOLE, 1GM, NEAT
ether,methylpentachlorophenyl
Methyl pentachlorophenyl ester
Methyl pentachlorophenyl ether
Pentachlorophenol methyl ether
PENTACHLOROPHENOL METHYL ESTER
Pentachlorophenyl methyl ether
Pentachloroanisole 1g [1825-21-4]
Pentachloroanisole@100 μg/mL in MeOH
PentachloroanisoleSolution,200ug/L,1ml
PentachloroanisoleSolution,100mg/L,1ml
PentachloroanisoleSolution,200mg/L,1ml
1-Methoxy-2,3,4,5,6-pentachlorobenzene
1,2,3,4,5-Pentachloro-6-methoxybenzene
1,2,3,4,5-Pentachloro-6-methoxy-benzene
Benzene, 1,2,3,4,5-pentachloro-6-methoxy-
[Molecular Formula]

C7H3Cl5O
[MDL Number]

MFCD00129711
[MOL File]

1825-21-4.mol
[Molecular Weight]

280.36
Chemical PropertiesBack Directory
[Melting point ]

108-110℃
[Boiling point ]

309℃ (760 Torr)
[density ]

1.6178 (estimate)
[storage temp. ]

0-6°C
[solubility ]

Chloroform, Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
[EPA Substance Registry System]

Pentachloroanisole (1825-21-4)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

2811
[RTECS ]

BZ8820000
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[Hazardous Substances Data]

1825-21-4(Hazardous Substances Data)
Hazard InformationBack Directory
[Uses]

2,3,4,5,6-Pentachloroanisole is a pesticide. One of the new POPs under the Stockholm Convention
[General Description]

Needles or white crystals.
[Air & Water Reactions]

Insoluble in water.
[Reactivity Profile]

A halogenated ether derivative. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert. Simple aromatic halogenated organic compounds are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms.
[Fire Hazard]

Flash point data for PENTACHLOROANISOLE are not available; however, PENTACHLOROANISOLE is probably combustible.
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