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84418-31-5

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84418-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84418-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,1 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84418-31:
(7*8)+(6*4)+(5*4)+(4*1)+(3*8)+(2*3)+(1*1)=135
135 % 10 = 5
So 84418-31-5 is a valid CAS Registry Number.

84418-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[hydroxy(propan-2-yl)amino]-3-naphthalen-1-yloxypropan-2-ol

1.2 Other means of identification

Product number -
Other names N-Hydroxypropranolol

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:84418-31-5 SDS

84418-31-5Downstream Products

84418-31-5Relevant articles and documents

Comparative study on degradation of propranolol and formation of oxidation products by UV/H2O2 and UV/persulfate (PDS)

Yang, Yi,Cao, Ying,Jiang, Jin,Lu, Xinglin,Ma, Jun,Pang, Suyan,Li, Juan,Liu, Yongze,Zhou, Yang,Guan, Chaoting

, p. 543 - 552 (2019/01/05)

The frequent detection of propranolol, a widely used β-blocker, in wastewater effluents and surface waters has raised serious concern, due to its adverse effects on organisms. UV/hydrogen peroxide (UV/H2O2) and UV/persulfate (UV/PDS) processes are efficient in eliminating propranolol in various waters, but the formation of oxidation products in these processes, as well as the assessment of their toxicity, has not been systematically addressed. In this study, we identified and compared transformation products of propranolol produced by hydroxyl radical (?OH) and sulfate radical (SO4?-). The electrostatic attraction enhances the reaction between SO4?- and the protonated form of propranolol, while ?OH shows non-selectivity toward both protonated and neutral propranolol species. The hydroxylation of propranolol by ?OH occurs at either amine moiety or naphthalene group while SO4?- favors the oxidation of the electron-rich naphthalene group. Further oxidation by ?OH and SO4?- results in ring-opening products. Bicarbonate and chloride exert no effect on propranolol degradation. The generation of CO3?- and Cl-containing radicals is favorable to oxidizing naphthalene group. The acute toxicity assay of Vibrio fischeri suggests that SO4?- generates more toxic products than ?OH, while CO3?- and Cl-containing radicals produce similar toxicity as SO4?-. High concentrations of bicarbonate in UV/H2O2 increase the toxicity of treated solution.

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