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ChemicalBook--->CAS DataBase List--->83130-01-2

83130-01-2

83130-01-2 Structure

83130-01-2 Structure
IdentificationBack Directory
[Name]

ALANYCARB
[CAS]

83130-01-2
[Synonyms]

ORION
ok135
ALANYCARB
Mianlingwei
Alanycarb [iso]
Orion【pesticide】
ALANYCARB STANDARD
ALANYCARB USP/EP/BP
ethylester,(z)-ylmethyl)
Alanycarb Solution in Acetonitrile, 1000μg/mL
5-oxa-2,8-dithia-4,7,9-triazadodec-3-en-12-oicacid,3,7-dimethyl-6-oxo-9-(phen
(Z)-ethyl-3,7-dimethyl-6-oxo-9-(phenyl methyl)-5-oxa-2,8-dithia-4,7,9-triazadodec-3-en-12-oate
6,10-Dimethyl-7-oxo-4-(phenylmethyl)-8-oxa-5,11-dithia-4,6,9-triazadodec-9-enoic acid ethyl ester
(Z)-9-Benzyl-3,7-dimethyl-6-oxo-5-oxa-2,8-dithia-4,7,9-triazadodecan-3-en-12-oic acid ethyl ester
Ethyl=(Z)-3-[N-benzyl-N-[[methyl(1-methylthioethylidenaminooxycarbonyl)amino]thio]amino]propionate
8-Oxa-5,11-dithia-4,6,9-triazadodec-9-enoic acid, 6,10-dimethyl-7-oxo-4-(phenylmethyl)-, ethyl ester, (9Z)-
5-Oxa-2,8-dithia-4,7,9-triazadodec-3-en-12-oic acid, 3,7-dimethyl-6-oxo-9-(phenylmethyl)-, ethyl ester, (Z)-
[Molecular Formula]

C17H25N3O4S2
[MDL Number]

MFCD00274585
[MOL File]

83130-01-2.mol
[Molecular Weight]

399.53
Chemical PropertiesBack Directory
[Melting point ]

47~52℃
[Boiling point ]

506.2±60.0 °C(Predicted)
[density ]

1.18
[vapor pressure ]

﹤4.7×10-6pa at 20°C
[storage temp. ]

2-8°C
[solubility ]

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

neat
[pka]

0.37±0.70(Predicted)
[Water Solubility ]

20 mg l-1 in water (20 °C)
Safety DataBack Directory
[Hazard Codes ]

T+,N
[Risk Statements ]

22-26-50
[Safety Statements ]

28-36/37-45-61
[RIDADR ]

UN2811 - class 6.1 - PG 2 - EHS - Toxic solids, organic, n.o.s., HI: all
[WGK Germany ]

3
[RTECS ]

RO0965000
Hazard InformationBack Directory
[Uses]

Alanycarb is a broad spectrum oxime carbamate insecticide with both contact and oral toxicity to a wide variety of insect pests, especially Lepidoptera, Coleoptera, Hemiptera and Thysanoptera, in/on grapes, pome fruits, tobacco and vegetables. Alanycarb can be applied as foliar, soil or seed treatments.
[Uses]

Alanycarb is a oxime carbamate inseciticide with acetylcholinesterase inhibitor activity.
[Uses]

Alanycarb may be used as an analytical reference standard for the determination of the analyte in:
  • Olive oil samples by fast liquid chromatography-electrospray time-of-flight mass spectrometry (LC-TOFMS).
  • Vegetables and fruit juices by LC coupled to tandem mass spectrometry (MS/MS).

[Definition]

ChEBI: Alanycarb is a carbamate ester and an ethyl ester. It has a role as a carbamate insecticide, an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an agrochemical and a nematicide.
[General Description]

Alanycarb is classified under the oxime carbamate group of insecticides. Its mode of action involves the inhibition of cholinesterase enzyme.
[Metabolic pathway]

Alanycarb is a pro-insecticide which transforms either chemically or biologically into the active substance methomyl. Alanycarb metabolism in soil, plants and animals follows a common pathway that is consistent with methomyl. The primary metabolic pathway involves the initial cleavage of the N-S bond of alanycarb to yield methomyl and ethyl N-benzyl-β-alaninate. Methomyl is further metabolised to S-methyl-N-hydroxythioacetimidate and ultimately to acetonitrile, acetic acid and carbon dioxide (Scheme 1). See also the methomyl entry.
[Degradation]

Alanycarb (1) was stable to hydrolytic degradation in neutral and weakly basic solutions (pH 7 and 9) at 30 °C with DT50 of 49 hours and 130 hours, respectively. It degraded rapidly (DT50 0.5 hours) in acidic solution (pH 5) at 20 °C (Yagi and Kawata, 1992). In acidic buffer solution (pH 4.0), the major hydrolytic degradation product was methomyl (2). The disulfide derivative (3) of alanycarb was observed as a minor product. In pH 7 and 9 solutions, hydrolysis of methomyl [S-methyl-N-hydroxythioacetimidate (4)] occurred and polar unknown products were found as major degradation products (Kawata, 1994).
Alanycarb degraded rapidly under xenon lamp irradiation (light intensity: 280-300 μEm-2 s-1) in distilled water with a DT50 of 9.3 hours (Yagi and Kawata, 1993).
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