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Bismuth, dihydroxytriphenyl-, also known as bismuth phenolate or bismuth subgallate, is a chemical compound with the formula C18H12BiO4. It is a yellow crystalline solid that is insoluble in water but soluble in alcohol and ether. Bismuth, dihydroxytriphenyl- is primarily used in the pharmaceutical industry as an antiseptic and astringent, particularly for the treatment of gastrointestinal disorders such as diarrhea and peptic ulcers. It works by forming a protective layer on the mucosal surface, which helps to reduce irritation and inflammation. Additionally, bismuth, dihydroxytriphenyl- has been studied for its potential antiviral and antibacterial properties, although its use in these applications is less common. The compound is generally considered safe and well-tolerated, with minimal side effects.

4663-81-4

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4663-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4663-81-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4663-81:
(6*4)+(5*6)+(4*6)+(3*3)+(2*8)+(1*1)=104
104 % 10 = 4
So 4663-81-4 is a valid CAS Registry Number.

4663-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenylbismuth dihydroxide

1.2 Other means of identification

Product number -
Other names Triphenylbismutdihydroxid

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:4663-81-4 SDS

4663-81-4Relevant academic research and scientific papers

Diverse structures and remarkable oxidizing ability of triarylbismuthane oxides. Comparative study on the structure and reactivity of a series of triarylpnictogen oxides

Matano, Yoshihiro,Nomura, Hazumi,Hisanaga, Teppei,Nakano, Haruyuki,Shiro, Motoo,Imahori, Hiroshi

, p. 5471 - 5480 (2008/10/09)

A systematic series of triarylbismuthane oxides was prepared in order to disclose their structure and reactivity, which have been compared with those of lighter pnictogen counterparts. X-ray crystallographic analysis of tris(2-methoxyphenyl)bismuthane oxide and tris(2-methoxyphenyl)stibane oxide revealed that they exist as dimers with a flat bis(a-oxo) ring, implying that the polarized Bi+-O- and Sb+-O- bonds aggregate to attain electrostatic stabilization. In sharp contrast to their phosphorus, arsenic, and antimony counterparts, triarylbismuthane oxides are thermally unstable and possess a high oxidizing ability. In particular, the bismuthane oxides bearing ortho-substituted aryl ligands oxidized primary and secondary alcohols to aldehydes and ketones, respectively, with high efficiency under mild conditions.

Reactions of triarylbismuth bis(arenesulfonates)

Sharutin,Sharutina,Egorova,Ettenko

, p. 1236 - 1237 (2007/10/03)

Reactions of triphenylbismuth with sodium salts, acids, alkalies, and zinc are studied. In the first three cases Bi-O bond cleavage takes place, while zinc reduces the starting bismuth compounds to triphenylbismuth.

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