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Trimethyl (phosphorothioyltrimethanediyl)triscarbamate is a chemical compound synthesized by the combination of three units of trimethyl phosphorodithioate with one unit of carbon dioxide. It is characterized by its potent insecticidal and acaricidal properties, which are utilized in agricultural settings to manage a broad spectrum of pests.

63833-14-7

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63833-14-7 Usage

Uses

Used in Agricultural Industry:
Trimethyl (phosphorothioyltrimethanediyl)triscarbamate is used as an insecticide and acaricide for controlling a variety of pests such as mites, aphids, and caterpillars. It operates by disrupting the nervous system of the target pests, resulting in paralysis and ultimately death. Recognized for its high toxicity to insects and comparatively low toxicity to mammals, trimethyl (phosphorothioyltrimethanediyl)triscarbamate offers an effective and relatively safe method for pest management in agriculture. However, adherence to label instructions and safety guidelines is crucial to mitigate any potential risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 63833-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,3 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63833-14:
(7*6)+(6*3)+(5*8)+(4*3)+(3*3)+(2*1)+(1*4)=127
127 % 10 = 7
So 63833-14-7 is a valid CAS Registry Number.

63833-14-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-[bis[(methoxycarbonylamino)methyl]phosphinothioylmethyl]carbamate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63833-14-7 SDS

63833-14-7Downstream Products

63833-14-7Relevant academic research and scientific papers

Process for the preparation of tris(N-carbalkoxylaminomethyl)phosphine oxides and sulfides

-

, (2008/06/13)

The title compounds, having the formula (RO2 CNHCH2)3 PY where Y=oxygen or sulfur, are prepared by reacting a tetrakis(N-carbalkoxylaminomethyl)phosphonium salt having the formula (RO2 CNHCH2)4 P+ X- with ammonia or a primary or secondary amine, followed by an oxidizing or sulfurizing agent. The products, after methylolation with formaldehyde, are useful as finishing agents for imparting flame retardant properties to cotton fabrics.

Tris(N-carbalkoxylaminomethyl)phosphine oxides and sulfides

-

, (2008/06/13)

The title compounds, having the formula (RO2 CNHCH2)3 PY where Y=oxygen or sulfur, are prepared by reacting a tris(N-carbalkoxylaminomethyl)phosphine, having the formula (RO2 CNHCH2)3 P, with an oxidizing or sulfurizing agent. The products, after methylolation with formaldehyde, are useful as finishing agents for imparting flame retardant properties to cotton fabrics.

Synthesis of tris(aminomethyl)phosphine oxide and its carbon dioxide adduct from tetrakis(hydroxymetyl)phosphonium salts via their methyl carbamate derivatives

Frank, Arlen W.

, p. 27 - 33 (2007/10/02)

Tris(aminomethyl)phosphine oxide (6) can be synthesized from octakis(hydroxymethyl)diphosphonium sulfate (1b) in an overall yield of 54.6percent via the methyl carbamate derivatives 2b, 3, and 4.On a preparative scale, the last step is complicated by the formation of a cyclic by-product 8 in amounts up to 20percent of the total.The triamine 6 forms a 1:1 adduct (11) with carbon dioxide, whose structure, established by 1H and 13C nmr, consists of equimolar amounts of carbamate A and dicarbamate BC.The components A, B, and C can be separated by ion exchange.Thjermolysis of 11 regenerates 6 smoontly, providing a convenient method for purifying the triamine.

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