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PH 800/20 is a specialized chemical mixture formulated to regulate and maintain the pH level in industrial water systems. It is composed of a synergistic blend of organic and inorganic acids, corrosion inhibitors, and dispersants, which work collectively to manage alkalinity and pH, safeguard metal surfaces from corrosion, and prevent scale formation and sedimentation. This formulation is crucial for the stability and optimal performance of water systems in various industrial applications.

176-02-3

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176-02-3 Usage

Uses

Used in Industrial Water Systems:
PH 800/20 is used as a pH control agent for maintaining the optimal pH level in industrial water systems, ensuring the prevention of corrosion and scale buildup.
Used in Boiler Systems:
In the context of boiler systems, PH 800/20 is used as a corrosion inhibitor to protect metal surfaces from degradation, thereby extending the equipment's lifespan and ensuring efficient operation.
Used in Cooling Towers:
PH 800/20 is utilized as a dispersant in cooling towers to prevent scale buildup and sedimentation, which can hinder heat transfer and lead to system inefficiencies.
Used in Wastewater Treatment Systems:
Within wastewater treatment systems, PH 800/20 is employed to manage the pH level, which is critical for the biological processes involved in wastewater treatment, as well as to control the corrosiveness of the wastewater to the treatment infrastructure.

Check Digit Verification of cas no

The CAS Registry Mumber 176-02-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,7 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176-02:
(5*1)+(4*7)+(3*6)+(2*0)+(1*2)=53
53 % 10 = 3
So 176-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8S4/c1-5(2-7-6-1)3-8-9-4-5/h1-4H2

176-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,7,8-Tetrathiaspiro[4.4]nonane

1.2 Other means of identification

Product number -
Other names PH 800/20

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:176-02-3 SDS

176-02-3Relevant academic research and scientific papers

Molecular rods based on oligo-spiro-thioketals

Wessig,Gerngro?,Freyse,Bruhns,Przezdziak,Schilde,Kelling

, p. 1125 - 1136 (2016/02/19)

We report on an extension of the previously established concept of oligospiroketal (OSK) rods by replacing a part or all ketal moieties by thioketals leading to oligospirothioketal (OSTK) rods. In this way, some crucial problems arising from the reversible formation of ketals are circumvented. Furthermore, the stability of the rods toward hydrolysis is considerably improved. To successfully implement this concept, we first developed a number of new oligothiol building blocks and improved the synthetic accessibility of known oligothiols, respectively. Another advantage of thioacetals is that terephthalaldehyde (TAA) sleeves, which are too flexible in the case of acetals can be used in OSTK rods. The viability of the OSTK approach was demonstrated by the successful preparation of some OSTK rods with a length of some nanometers.

Synthesis and Thermal Stability of 4-Substituted 1,2-Dithiolanes

Teuber, Lene,Christophersen, Carsten

, p. 629 - 634 (2007/10/02)

Disodium 2-cyano-3,3-bis(sulfido)propenamide (6) has been used as a double synthon for SH- in the preparation of 1,3-dithiols.Oxidation of the dithiols gives 4-substituted 1,2-dithiolanes, e.g. asparagusic acid (3).The energy splits between the first and second ionization potantials in 3 and the other 1,2-dithiolanes (8-11) have been determined by ultraviolet photoelectron spectroscopy.The relative stability of these compounds do not correlate with the measured ΔE values.Hence, factors besides the S-S torsional angle must influence these stabilities.

SYNTHESIS OF NEW MACROCYCLIC POLYTHIAETHER

Fujihara, Hisashi,Imaoka, Koji,Furukawa, Naomichi,Oae, Shigeru

, p. 1701 - 1704 (2007/10/02)

Synthesis of a new macrocyclic polythiaether (12) which is easily obtained in a good yield via 2,6-dithia-4-spiroheptane (6) is described.Several reactions of pentaerythrityl bromide (1) with nucleophiles and a few ring opening reactions of 6 with methyl iodide are also described.

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