Welcome to LookChem.com Sign In|Join Free

CAS

  • or

696-28-6

Post Buying Request

696-28-6 Suppliers

Recommended suppliersmore

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

696-28-6 Usage

Chemical Properties

Phenyldichloroarsine is a colorless or light yellow liquid or gas. Odorless.

General Description

A colorless odorless liquid. Density 1.654 g / cm3. Used as a lachrymator poison gas. Toxic by inhalation and skin absorption.

Air & Water Reactions

Reacts with water or with moist air to form hydrochloric acid [AAR 1991].

Reactivity Profile

PHENYL DICHLOROARSINE is incompatible with acids and bases. A reducing agents and therefore generally incompatible with oxidizing agents.

Health Hazard

Median lethal dosage 2600 mg-minute/m3. Mean incapacitating dosage 16 mg-minute/m3 as a vomiting agent and 1800 mg-minute/m3 as a blistering agent. 633 mg-minute/m3 produces eye injury. Poisonous; may be fatal if inhaled, swallowed, or absorbed through skin. Contact may cause burns to skin and eyes. Strong irritant to eyes, skin, and issue.

Fire Hazard

PHENYL DICHLOROARSINE may burn but does not ignite readily. Containers may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Upon decomposition hydrogen chloride and phenylarsenious oxide are emitted. Unstable. Decomposed by water.

Safety Profile

Poison by inhalation, ingestion, skin contact, and intravenous routes. See also ARSENIC. A lachrymator type of dtary poison gas. When exposed to heat, water, or steam it reacts to produce corrosive fumes of Cl-. When heated to decomposition it emits highly toxic fumes of arsenic.

Potential Exposure

Phenyldichloroarsine is an organoarsenic compound used in organic synthesis and as a solvent. PD has been used as a military tear gas, vesicant and blister agent.

Shipping

UN3280 Organoarsenic compound, liquid, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required, Potential Inhalation Hazard (Special Provision 5). UN1556 Arsenic compounds, liquid, n.o.s. inorganic, including arsenates, n.o.s.; arsenites, n.o.s.; arsenic sulfides, n.o.s.; and organic compounds of arsenic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. Military driver shall be given full and complete information regarding shipment and conditions in case of emergency. AR 50-6 deals specifically with the shipment of chemical agents. Shipments of agent will be escorted in accordance with AR 740-32.

Incompatibilities

Contact with water forms HCl. Heat produces fumes of arsenic and chlorine. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Attacks some metals in the presence of moisture

Check Digit Verification of cas no

The CAS Registry Mumber 696-28-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 696-28:
(5*6)+(4*9)+(3*6)+(2*2)+(1*8)=96
96 % 10 = 6
So 696-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H5AsCl2/c8-7(9)6-4-2-1-3-5-6/h1-5H

696-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloro(phenyl)arsane

1.2 Other means of identification

Product number -
Other names Phenyl dichloroarsine

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:696-28-6 SDS

696-28-6Relevant articles and documents

Geminally Substituted Tris(acenaphthyl) and Bis(acenaphthyl) Arsines, Stibines, and Bismuthine: A Structural and Nuclear Magnetic Resonance Investigation

Chalmers, Brian A.,Meigh, Christina B. E.,Nejman, Phillip S.,Bühl, Michael,Lébl, Tomá?,Woollins, J. Derek,Slawin, Alexandra M. Z.,Kilian, Petr

, p. 7117 - 7125 (2016)

Tris(acenaphthyl)- and bis(acenaphthyl)-substituted pnictogens (iPr2P-Ace)3E (2-4) (E = As, Sb, or Bi; Ace = acenaphthene-5,6-diyl) and (iPr2P-Ace)2EPh (5 and 6) (E = As or Sb) were synthesized and fully characterized by multinuclear nuclear magnetic resonance (NMR), high-resolution mass spectrometry, elemental analysis, and single-crystal X-ray diffraction. The molecules adopt propeller-like geometries with the restricted rotational freedom of the sterically encumbered iPr2P-Ace groups resulting in distinct NMR features. In the tris(acenaphthyl) species (2-4), the phosphorus atoms are isochronous in the 31P{1H} NMR spectra, and the rotation of the three acenaphthyl moieties around the E-Cipso bond is locked. On the other hand, the bis(acenaphthyl) species show a fluxional behavior, resulting in an AX to A2 spin system transition in the 31P{1H} variable-temperature NMR spectra. This allowed elucidation of remarkable through-space couplings (8TSJPP) of 11.5 Hz (for 5) and 25.8 Hz (for 6) at low temperatures. In addition, detailed line shape analysis of the thermodynamic parameters of the restricted rotation of the "propeller blades" in 5 was performed in the intermediate temperature region and also at coalescence. The lone pairs on the pnictogen atoms in 2-6 are oriented such that they form a bowl-shaped area that is somehow buried within the molecule.

(2-Pyridyloxy)arsines as ligands in transition metal chemistry: a stepwise As(iii) → As(ii) → As(i) reduction

Gericke, Robert,Wagler, J?rg

, p. 10042 - 10051 (2020)

Neutral inherently tri- and tetradentate ligands of the type Ph3-xAs(PyO)x (x = 2 (1), 3 (2)) have been synthesized and characterized. Reaction of 1 with [RuCl2(PPh3)3] affords complex [PhAs(μ-PyO)2RuCl2(PPh3)] (3), whereas 2 and [RuCl2(PPh3)3] react with formation of [As(μ-PyO)2RuCl(PPh3)2] (5) and [Ph3P(PyO)]Cl (6). Treatment of complex 5 with [AuCl(tht)] (tht = tetrahydrothiophene) results in liberation of tht and formation of [AuCl(As(PyO)2)RuCl(PPh3)2] (7), featuring an (Au-As-Ru) core. For compounds 3, 5, and 7 the As-Ru and As-Au bond situation has been investigated using NBO, AIM and ELF analysis, allowing the assignment of pronounced canonical forms of σ-(AsIII→RuII) to 3, σ-(AsII-RuI) to 5 and σ-(AuI←AsI→RuII) to 7. This journal is

Oral administration of diphenylarsinic acid, a degradation product of chemical warfare agents, induces oxidative and nitrosative stress in cerebellar Purkinje cells

Kato, Koichi,Mizoi, Mutsumi,An, Yan,Nakano, Masayuki,Wanibuchi, Hideki,Endo, Ginji,Endo, Yoko,Hoshino, Mikio,Okada, Shoji,Yamanaka, Kenzo

, p. 1518 - 1525 (2008/03/14)

A new clinical syndrome with prominent cerebellar symptoms in patients living in Kamisu City, Ibaraki Prefecture, Japan, is described. Since the patients ingested drinking water containing diphenylarsinic acid (DPA), a stable degradation product of both diphenylcyanoarsine and diphenylchloroarsine, which were developed for use as chemical weapons and cause severe vomiting and sneezing, DPA was suspected of being responsible for the clinical syndrome. The purpose of the present study was to elucidate prominent cerebellar symptoms due to DPA. The aim of the study was to determine if single (15 mg/kg) or continuous (5 mg/kg/day for 5 weeks) oral administration of DPA to ICR-strain mice induced oxidative and/or nitrosative stress in their brain. Significantly positive staining with malondialdehyde (MDA) and 3-nitrotyrosine (3-NT) was observed in the cerebellar Purkinje cells by repeated administration (5 mg/kg/day) with DPA for 5 weeks that led to the cerebellar symptoms from a behavioral pharmacology standpoint and by single administration of DPA (15 mg/kg). Furthermore, it is possible that the production of 3-NT was not caused by peroxynitrite formation. The present results suggest the possibility that arsenic-associated novel active species may be a factor underlying the oxidative and nitrosative stress in Purkinje cells due to exposure to DPA, and that the damage may lead to the cerebellar symptoms.