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1445-76-7

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1445-76-7 Usage

Description

2-Propyl methylphosphonochloridate, also known as cyclosarin (GF), is a liquid nerve agent belonging to the organophosphate class and contains fluoride. It is a colorless liquid with an odor that is variously described as nondescript, sweet, or fruit-like. The odor threshold for cyclosarin is approximately 12 milligrams per cubic meter.

Uses

Used in Military Applications:
2-Propyl methylphosphonochloridate is used as a chemical warfare agent due to its high toxicity and rapid onset of effects. It is designed to incapacitate and potentially kill enemy personnel by disrupting the nervous system, leading to symptoms such as muscle twitching, difficulty breathing, and seizures.
Used in Research and Development:
In the field of chemical research, 2-propyl methylphosphonochloridate serves as a starting material or reagent for the synthesis of various organophosphate compounds. It is also used to study the effects of nerve agents on biological systems and to develop countermeasures and antidotes for potential exposure.
Used in Detection and Protection:
2-Propyl methylphosphonochloridate is utilized in the development of detection systems and protective equipment for military and civilian applications. These systems are designed to identify the presence of nerve agents, such as cyclosarin, and provide protection against their harmful effects.

Potential Exposure

A quick-acting and lethal cholinester- ase inhibitor and casualty agent. Females appear to be more susceptible to nerve agent effects. Small percentages of general population have genetic traits that may increase susceptibility.

Shipping

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatibilities

Fairly stable. Cyclo-sarin (GF) is hydro- lyzed by water; rapidly hydrolyzed in the presence of heat and alkalies; by dilute solution of aqueous sodium hydrox- ide. Contact with alkaline conditions produce isopropyl alcohol and polymer substances. Contact with acid condi- tions produce HF; alkaline conditions produce isopropyl alcohol and polymers. Reasonably stable when stored in steel at normal temperatures; slightly corrosive to steel when heated.

Waste Disposal

Principles and methods for destruction of chemical weapons: “Destruction of chemical weapons” means a process by which chemicals are con- verted in an essentially irreversible way to a form unsuitable for production of chemical weapons, and which in an irreversible manner renders munitions and other devices unusable as such. Each nation shall determine how it shall destroy chemical weapons, except that the following processes may not be used: dumping in any body of water, land burial or open-pit burning. It shall destroy chemical weapons only at specifically designated and appropriately designed and equipped facilities. Each nation shall ensure that its chemical weapons destruction facilities are con- structed and operated in a manner to ensure the destruction of the chemical weapons; and that the destruction process can be verified under the provisions of this Convention. (Organization for the Prohibition of Chemical Weapons; Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons and Their Destruction). Grossly liquid-contaminated materials should be decontaminated and containerized and labeled in accordance with DOT and EPA requirements as a hazwaste. Wastewater solution from decon should be analyzed to ensure no residual agent is present. The National Response Plan, ESF-3 designates United States Army Corps of Engineers (USACE) as the primary agency to manage con- taminated debris. USACE and the Department of Defence (DOD) typically use safety procedures prior to transport that include “head space” (off gas) monitoring around containers prior to shipment to ensure no leakage/off-gassing. Typically waste will be transported in accordance with state require- ments to a designated disposal facility, such as a RCRA- permitted hazardous waste facility (typically an incinerator). Wastewater solution from the decontamination process will be analyzed to ensure no residual agent is present. It is likely that the solution will not contain residual agents and there- fore not need to be classified as a hazardous waste but sam- pling must be used to verify. Chlorinated wastewater may need to be treated/neutralized prior to disposal . United States munitions stockpiles of G-agent are/have undergone destruction/disposal in the states of Utah, Oregon, Arkansas, Alabama, and Kentucky. State/local plans to address poten- tial releases from United States Army properties are in place at these sites.

Check Digit Verification of cas no

The CAS Registry Mumber 1445-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1445-76:
(6*1)+(5*4)+(4*4)+(3*5)+(2*7)+(1*6)=77
77 % 10 = 7
So 1445-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H10ClO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3

1445-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methylethyl methylphosphonochloridate

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:1445-76-7 SDS

1445-76-7Relevant articles and documents

Analogues with fluorescent leaving groups for screening and selection of enzymes that efficiently hydrolyze organophosphorus nerve agents

Brise?o-Roa, Luis,Hill, Jim,Notman, Stuart,Sellers, David,Smith, Andy P.,Timperley, Christopher M.,Wetherell, Janet,Williams, Nichola H.,Williams, Gareth R.,Fersht, Alan R.,Griffiths, Andrew D.

, p. 246 - 255 (2006)

Enzymes that efficiently hydrolyze highly toxic organophosphorus nerve agents could potentially be used as medical countermeasures. As sufficiently active enzymes are currently unknown, we synthesized twelve fluorogenic analogues of organophosphorus nerve agents with the 3-chloro-7-oxy-4- methylcoumarin leaving group as probes for high-throughput enzyme screening. This set included analogues of the pesticides paraoxon, parathion, and dimefox, and the nerve agents DFP, tabun, sarin, cyclosarin, soman, VX, and Russian-VX. Data from inhibition of acetylcholinesterase, in vivo toxicity tests of a representative analogue (cyclosarin), and kinetic studies with phosphotriesterase (PTE) from Pseudomonas diminuta, and a mammalian serum paraoxonase (PON1), confirmed that the analogues mimic the parent nerve agents effectively. They are suitable tools for high-throughput screens for the directed evolution of efficient nerve agent organophosphatases.

Synthesis of the Tripeptides Tyr-Thr-Lys Phosphorylated with Isopropyl Methyl- and (Deuteromethyl)phosphonochloridates as Reference Standards for the Analysis of Biomedical Samples

Rodin,Baygildiev,Krylov,Osipov,Krylov,Yashkir,Rybalchenko

, p. 2103 - 2107 (2019/11/29)

A procedure for the phosphorylation of the tripeptide Tyr-Thr-Lys with isopropyl methyl- or (deuteromethyl)phosphonochloridate is developed. The phosphorylated tripeptides are intended for use as reference standards in the analysis of blood samples of people suspected to have been exposed to acetylcholinesterase inhibitors. Conditions of hromatographic separation and purification of the synthesized compounds are determined and optimized, which ensures the preparation of high-purity phosphorylated tripeptides.

New method for synthesizing substituted phosphinate

-

Paragraph 0022; 0025-0026, (2017/12/27)

The invention discloses a new method for synthesizing substituted phosphinate. The method comprises the step of generating the substituted phosphinate by reducing halogenated phosphonate under the effect of a reducing agent. The optimal preparation method for the substituted phosphinate is screened through a large number of experiments according to the invention; the whole process is reasonably designed; the technological operation is simple and efficient; especially, the optimal reaction conditions are screened, including reaction solvent, reaction temperature, reaction time and optimal reaction pH value; the reaction yield is obviously increased; the yield reaches up to 85-95%; the side reaction is less; the production cost is greatly lowered; the industrial production can be realized; and the method has a wide application prospect.

Phosphylated tyrosine in albumin as a biomarker of exposure to organophosphorus nerve agents

Williams, Nichola H.,Harrison, John M.,Read, Robert W.,Black, Robin M.

, p. 627 - 639 (2008/03/13)

The organophosphorus nerve agents sarin, soman, cyclosarin and tabun phosphylate a tyrosine residue on albumin in human blood. These adducts may offer relatively long-lived biological markers of nerve agent exposure that do not 'age' rapidly, and which ar

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