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Phenylmercury, a class of organomercury compounds, is characterized by the presence of a phenyl group (C6H5) bonded to a mercury atom. These compounds are typically used as catalysts, fungicides, and disinfectants due to their ability to inhibit microbial growth. However, they are also known for their neurotoxicity and potential to cause severe health issues, including damage to the nervous system and kidneys. As a result, their use has been restricted or banned in many countries due to environmental and health concerns. Phenylmercury compounds are persistent in the environment and can accumulate in the food chain, posing a risk to both wildlife and human populations.

5980-94-9

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5980-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5980-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,8 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5980-94:
(6*5)+(5*9)+(4*8)+(3*0)+(2*9)+(1*4)=129
129 % 10 = 9
So 5980-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H6S.C6H5.Hg/c7-6-4-2-1-3-5-6;1-2-4-6-5-3-1;/h1-5,7H;1-5H;/q;;+1/p-1/rC6H5Hg.C6H6S/c2*7-6-4-2-1-3-5-6/h1-5H;1-5,7H/q+1;/p-1

5980-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl(phenylsulfanyl)mercury

1.2 Other means of identification

Product number -
Other names phenylmercury (1+),thiophenolate

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:5980-94-9 SDS

5980-94-9Downstream Products

5980-94-9Relevant academic research and scientific papers

Mercury(II) and organomercury(II) complexes of thiols and dithiols, including british anti-lewisite

Canty,Kishimoto

, p. 109 - 122 (2008/10/09)

The dithiols 2,3-dimercapto-1-propanol (British anti-Lewisite) and1,3-dimercapto-2propanol form complexes RHgS～SHgR (R = Me, Ph). The PhHg(II) complexes decompose in benzene and methanol at ambient temperature to form diphenylmercury. A 1:1 complex of Hg(II) with 1,3-dimercapto-2-propanol is dimeric in pyridine. Infrared, Raman, and 1H NMR spectra of RHg(II) and Hg(II) dithiol complexes are compared with those of PhHgSR (R = Me, Et, Pri, But, Ph, CH2CH2OH) and Hg(SR′)2 (R′ = Me, Et,But′, Ph, CH2CH2OH). Phenylmercury(II) thiolates have the coupling constant J(orthoH-199Hg) within the range 144-155 Hz. The complexes PhHgSR and Hg(SR″)2 (R″ = Et, But, Ph) are monomeric in chloroform; the chloroform insoluble complexes Hg(SR?)2 (R? = Me,CH2CH2OH) and organomercury(II) dithiolates are monomeric in pyridine. Aspects of the use of British anti-Lewisite as an antidote for mercury poisoning are discussed.

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