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1809326-44-0

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1809326-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1809326-44-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,9,3,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1809326-44:
(9*1)+(8*8)+(7*0)+(6*9)+(5*3)+(4*2)+(3*6)+(2*4)+(1*4)=180
180 % 10 = 0
So 1809326-44-0 is a valid CAS Registry Number.

1809326-44-0Downstream Products

1809326-44-0Relevant articles and documents

Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts

Jakimska, Anna,?liwka-Kaszyńska, Magdalena,Nagórski, Piotr,Namies?nik, Jacek,Kot-Wasik, Agata

, (2014)

Nowadays, monitoring focuses on the primary compounds and does not include degradation products formed during various biological and chemical processes. Transformation products may have the same effects to human health and the environment or sometimes they can be more toxic than the parent compound. Unfortunately, knowledge about the formation of degradation products is still limited, however, can be very important for the environmental risk assessment. Firstly, the photodegradation kinetic of amlodipine was investigated in two experimental conditions: during the exposure to solar radiation and during the exposure to the light emitted by the xenon lamp. In all cases degradation of amlodipine followed a pseudo-first-order kinetics. In the next step, identification of transformation products of amlodipine formed during the exposure to xenon lamp irradiation was performed using ultra high performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTOF-MS). As a result sixteen photoproducts were identified, their structures were elucidated and ultimately the transformation pathway was proposed. Fifteen compounds (out of 16 photoproducts) were newly identified and reported here for the first time; some of those compounds were formed from the first photoproduct, amlodipine pyridine derivative. Several analytes were formed only in acidic or basic conditions. Furthermore, the occurrence of amlodipine and its identified degradation products was investigated in environmental waters. Only one out of 16 compounds was found in wastewater effluent. The possibility of the sorption of examined analytes to sewage sludge particles was discussed based on QSAR.

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