ChemicalBook--->CAS DataBase List--->140-57-8

140-57-8

140-57-8 Structure

140-57-8 Structure
IdentificationBack Directory
[Name]

ARAMITE
[CAS]

140-57-8
[Synonyms]

88R
CES
88-r
Aramit
Aratron
88r[qr]
ARAMITE
ARACIDE
Aramaite
ent16,519
Acaracide
ARACIDE(R)
ARAMITE(R)
Ortho-Mite
ENT 16,519
NSC 404155
Niagaramite
aracide[qr]
aratron[qr]
Aramite-15W
COMPOUND 88R
Aethylacrylat
ent16,519[qr]
ORTHO-MITE(R)
NIAGARMITE(R)
aramite (jmaf)
compound88r[qr]
aramite-15w[qr]
aramite solution
Aramite (Uniroyal)
Aramiteararamite-15W
Acrylsaeureaethylester
aramiteararamite-15w[qr]
Aramite,0.1mg/mlinHexane
2-(p-t-Butylphenoxy)-1-met
YKFRAOGHWKADFJ-UHFFFAOYSA-N
ARAMITE (100 UG/ML IN MEOH)
AramiteSolution,2000mg/L,1mL
ARAMITE, 1X5ML, 0.1MG/ML IN HEXANE
Aramite@2000 μg/mL in Dichloromethane
Aramite Solution in Methanol, 100μg/mL
Butylphenoxyisopropylchloroethylsulfite
TIANFUCHEM--High purity 140-57-8 ARAMITE
butylphenoxyisopropylchloroethylsulfite[qr]
Butylphenoxyisopropyl chloroethyl sulfite@CES
2-(p-tert-Butylphenoxy)-1-methylethyl sulfite
2-(p-butylphenoxy)isopropyl2-chloroethylsulfite
2-(p-Butylphenoxy)isopropyl 2-chloroethyl sulfite
1-(p-t-butylphenoxy)-2-propano2-chloroethylsulfite
2-(4-t-butylphenoxy)isopropyl-2-chloroethylsulfite
2-(4-t-Butylphenoxy)isopropyl-2-chloroethyl sulfite
2-(p-t-butylphenoxy)isopropyl2’-chloroethylsulphite
2-(p-butylphenoxy)-1-methylethyl2-chloroethylsulfite
2-(p-butylphenoxy)isopropyl-2-chloroethylsulfite[qr]
2-(4-t-butylphenoxy)isopropyl-2-chloroethyl sulphite
2-(p-t-butylphenoxy)isopropyl 2'-chloroethyl sulfite
2-(p-t-Butylphenoxy)isopropyl 2'-chloroethyl sulphite
2-(p-tert-Buytlphenoxy)isopropyl 2-chloroethyl sulfite
2-chloroethylsulphiteof1-(p-t-butylphenoxy)-2-propanol
2-(4-tert-Butylphenoxy)isopropyl-2-chloroethyl sulfite
2-(p-butylphenoxy)-1-methylethyl 2-chloroethyl sulfite
2[P-TERT-BUTYLPHENOXY]ISO-PROPYL-2-CHLOROETHYL SULFITE
2-(p-t-butylphenoxy)-1-methylethyl-2-chloroethylsulfite
2-chloroethyl1-methyl-2-(p-t-butylphenoxy)ethylsulphate
2-chloro-ethano2-(p-t-butylphenoxy)-1-methylethylsulfite
2-(p-tert-butylphenoxy)isopropyl2-chloroethylsulfite[qr]
2-Chloroethyl sulfite of 1-(p-t-butylphenoxy)-2-propanol
2-(p-t-Butylphenoxy)-1-methylethyl-2-chloroethyl sulfite
2-(p-t-butylphenoxy)isopropyl-2’-chloroethylsulphite[qr]
2-(p-t-butylphenoxy)-1-methylethyl2’-chloroethylsulphite
1-(4-tert-butylphenoxy)propan-2-yl 2-chloroethyl sulfite
2-(4-tert-butylphenoxy)-1-methylethyl2-chloroethylsulfite
2-chloroethylsulphiteof1-(p-tert-butylphenoxy)-2-propanol
2-(p-tert-Butylphenoxy)-1-methylethyl-2-choroethyl sulfite
2-(p-t-Butylphenoxy)-1-methylethyl 2'-chloroethyl sulphite
2-chloroethyl1-methyl-2-(p-t-butylphenoxy)ethylsulphate[qr]
2-Propanol, 1-(p-tert-butylphenoxy)-, 2-chloroethyl sulfite
2-CHLOROETHYL-1-METHYL-2-(P-TERT-BUTYLPHENOXY)ETHYL SULFITE
2-(p-t-butylphenoxy)-1-methylethylsulphiteof2-chloroethanol
2-(p-t-butylphenoxy)-1-methylethyl2’-chloroethylsulphite[qr]
2-(p-tert-Butylphenoxy)-1-methylethyl 2'-chloroethyl sulfite
2-(p-tert-butylphenoxy)-1-methylethyl2-chloroethylsulfite[qr]
2-(p-t-butylphenoxy)-1-methylethylsulphiteof2-chloroethanol[qr]
2-(p-tert-Butylphenoxy)-1-methylethyl sulfite of 2-chloroethanol
esterof2-chloroethanolwith2-(p-tert-butylphenoxy)-methylsulphite
Ethanol, 2-chloro-, 2-(p-tert-butylphenoxy)-1-methylethyl sulfite
beta-Chloroethyl-beta-(p-t-butylphenoxy)-alpha-methylethyl sulfite
beta-chloroethyl-beta-(p-t-butylphenoxy)-alpha-methylethylsulphite
2-(p-terc.butylfenoxy)isopropyl-2’-chlorethylesterkyselinysiricite
beta-Chloroethyl-beta-(p-t-butylphenoxy)-alpha'-methylethyl sulfite
beta-chloroethyl-beta’-(p-t-butylphenoxy)-alpha’-methylethylsulfite
sulfurousacid,2-(p-t-butylphenoxy)-1-methylethyl-2-chloroethylester
2-chloro-ethanoesterwith2-(p-tert-butylphenoxy)-1-methylethylsulfite
2-(p-terc.Butylfenoxy)isopropyl-2'-chlorethylester kyseliny siricite
2-(p-t-butylphenoxy)-1-methylethyl2-chloroethylesterofsulphurousacid
sulfurousacid,2-(p-tert-butylphenoxy)-1-methylethyl2-chloroethylester
sulfurousacid,2-(p-tert-butylphenoxy)-1-methylethyl-2-chloroethylester
Sulfurous acid, 2-(p-t-butylphenoxy)-1-methylethyl-2-chloroethyl ester
beta-chloroethyl-beta-(p-t-butylphenoxy)-alpha-methylethylsulphite[qr]
beta-chloroethyl-beta’-(p-t-butylphenoxy)-alpha’-methylethylsulfite[qr]
beta-chloroethyl-beta-(p-tert-butylphenoxy)-alpha-methylethylsulphite[qr]
2-(p-t-Butylphenoxy)-1-methylethyl 2-chloroethyl ester of sulphurous acid
Sulfurous acid, 2-(p-tert-butylphenoxy)-1-methylethyl 2-chloroethyl ester
sulfurousacid,2-chloroethyl-,2-(4-(1,1-dimethylethyl)phenoxy)-1-methylethy
sulfurousacid,2-chloroethyl2-(4-(1,1-dimethylethyl)phenoxy)-1-methylethyles
sulfurous acid [2-(4-tert-butylphenoxy)-1-methyl-ethyl] 2-chloroethyl ester
2-(p-tert-Butylphenoxy)-1-methylethyl 2-chloroethyl ester of sulfurous acid
Ethanol, 2-chloro-, ester with 2-(p-tert-butylphenoxy)-1-methylethyl sulfite
Aramite [R], 97% [2-Chloroethyl-1-methyl-2-{p-tert-butylphenoxy)ethyl sulfite]
Sulfurous acid, 2-chloroethyl 2-[4-(1,1-dimethylethyl)phenoxy]-1-methylethyl ester
[Molecular Formula]

C15H23ClO4S
[MDL Number]

MFCD00128042
[MOL File]

140-57-8.mol
[Molecular Weight]

334.86
Chemical PropertiesBack Directory
[Appearance]

Aramite is a heavy, dark-amber liquid.
[Melting point ]

-31.7°
[Boiling point ]

bp0.1 175°; bp7.0 200-210°
[density ]

1.195
[refractive index ]

nD20 1.5100 to 1.5118; nD27 1.5075
[storage temp. ]

0-6°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[color ]

Colourless to Pale Brown
[IARC]

2B (Vol. 5, Sup 7) 1987
[EPA Substance Registry System]

Aramite (140-57-8)
Hazard InformationBack Directory
[Uses]

Miticide.
[Potential Exposure]

Aramite is an organochlorine miticide and antimicrobial agent. Aramite is regulated by EPA under the Federal Insecticide, Fungicide, and Rodenticide Act and the Resource Conservation and Recovery Act. The significant regulatory action was a voluntary cancellation of the active ingredient registration by the sole producer in 1975.
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.
[Shipping]

UN2902 Pesticides, liquid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.
[Incompatibilities]

Incompatible with alkaline material, such as lime or Bordeaux mixture (slaked lime and copper sulfate solution).
[Description]

Aramite is a synthetic chlorinated hydrocarbon with molecular weight of 334.87 and density of 1.143 at 20°C. It is a clear, light-colored oil with melting point of 37.3 C and boiling point of 175 °C at 0.1 mm Hg. The technical grade aramite is a dark amber liquid. Aramite is soluble at 0.000 1% (practically insoluble) in water but is miscible in many organic solvents. It was sold as mixture in organic solvents at different strengths for further dilution and use. Aramite was used as a pesticide (acaricide) to control mites in plants and animals. Aramite was initially introduced to market around 1950. It was mostly used between 1950 and 1954 in greenhouses in the United States. Its manufacture and use were voluntarily discontinued due to its carcinogenic potential according to a US Environmental Protection Agency (EPA) notice dated 12 April 1977. However, there are reports of bans of aramite use in a few European countries, in 1987 (Lithuania), 1996 (Poland), and 1999 (Estonia). There is no information on the production, import, registration, marketing, stockpiling, and use of aramite in Russia. Occupational exposure through dermal contact and inhalation was possible during its use.
[Chemical Properties]

Aramite is a heavy, dark-amber liquid.
[Waste Disposal]

Acid or alkaline hydrolysis followed by flushing to sewer.
[Definition]

ChEBI: Aramite is an alkylbenzene.
[General Description]

Aramite is a carcinogenic acaricide, widely used against six spotted mite, European red mite and others affecting crops.
[Toxicity evaluation]

Aramite can be released directly into the environment through its use as an acaricide (miticide); however, this use has been discontinued. If released to soil, aramite is expected to have no mobility. Volatilization from moist soil surfaces is not expected to be an important fate process based on an estimated Henry’s Law constant of 1.9×10-7 atm m3 mol-1. Biodegradation data for aramite are not available, and if released into water, aramite is expected to adsorb to suspended solids and sediments based upon the estimated Koc of 2.0×10+4. Volatilization from water surfaces is not expected to be an important fate process based on this compound’s estimated Henry’s Law constant. Aramite’s potential for bioconcentration in aquatic organisms is very high. Functional groups of aramite are susceptible to hydrolysis; however, insufficient data are available to predict the relative importance or occurrence of chemical or biological degradation processes in water or soil. Aramite is hydrolyzed by alkalies and may contribute to degradation in soil or water. If released into air, aramite is expected to be physically removed by wet and dry deposition processes.
Safety DataBack Directory
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-36/37/38-48/20-62-40
[Safety Statements ]

53-16-36/37/39-45-36/37-24/25-23
[RIDADR ]

UN 1208 3/PG 2
[WGK Germany ]

2
[HS Code ]

29252900
[Safety Profile]

Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Experimental poison by intraperitoneal route. Moderately toxic to humans by ingestion. Moderately toxic experimentally by ingestion. Experimental reproductive effects. A pesticide. When heated to decomposition it emits toxic fumes of Cland SOx. See also ESTERS and SULFUROUS ACID.
[Hazardous Substances Data]

140-57-8(Hazardous Substances Data)
[Toxicity]

LD50 orally in rats: 3.90±0.28 g/kg (Oser, Oser)
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