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41063-31-4

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41063-31-4 Usage

Type of compound

Tertiary amine alcohol

Common uses

Raw material in the synthesis of pharmaceuticals, pesticides, and other organic compounds

Role in asymmetric synthesis

Chiral auxiliary

Primary use

Precursor in the production of pharmaceuticals such as propranolol

Medical application

Treatment of high blood pressure, angina, and other cardiovascular conditions

Potential applications

Anti-inflammatory agent, inhibition of certain cancer cell growth

Check Digit Verification of cas no

The CAS Registry Mumber 41063-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,6 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41063-31:
(7*4)+(6*1)+(5*0)+(4*6)+(3*3)+(2*3)+(1*1)=74
74 % 10 = 4
So 41063-31-4 is a valid CAS Registry Number.

41063-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(isopropylamino)-2-propanol

1.2 Other means of identification

Product number -
Other names β-Isopropylamino-isopropylalkohol

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:41063-31-4 SDS

41063-31-4Upstream product

41063-31-4Relevant articles and documents

Removal of metoprolol by means of photo-oxidation processes

Avilés-García, Osmín,Brewer, Sharon,Donkor, Kingsley,Espino-Valencia, Jaime,Mendoza-Zepeda, Arisbeht,Natividad, Reyna,Romero, Rubi

, (2021/07/07)

In this study, β-blocker metoprolol was degraded by photocatalysis and photo-Fenton catalyzed by doped TiO2. The effect of two main variables was elucidated, content and type of doping cation (Fe or Cu). The catalysts were synthesized by Evaporation-Induced Self-Assembly (EISA) method and their performance was compared with typical Degussa P25. All synthesized materials were found to be mesoporous with a specific surface in the range of 121–242 m2/g, they all exhibited anatase phase, and crystallites in the range of 6–10 nm. The use of X-ray photoelectron spectroscopy (XPS) allowed to establish not only the presence of the expected Ti4+ but also Ti3+ species. Cu2+ and Fe3+ species were also identified in the doped catalysts. It was found that the addition of Cu and Fe diminished the energy band gap of synthesized TiO2, from 3.20 eV to 2.58 and 2.64, respectively. The content of Cu is directly correlated with this effect. In photocatalysis, the doping of TiO2 did not have an effect of metoprolol degradation rate. This was improved, however, approximately 60% by the synthesized TiO2 compared to Degussa P25. On the other hand, the photo-Fenton-like process catalyzed by Cu-TiO2 exhibited the highest degradation (total removal) and mineralization extent (90%), being faster than the photocatalytic process and the UV-H2O2 system. Another difference between both methods, was the amount and type of intermediates generated. These were identified by LC-MS. Photo-Fenton catalyzed by Cu/TiO2 can be considered as an effective process with high oxidative power in the metoprolol degradation.

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