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1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purine-7-butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52083-48-4

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52083-48-4 Usage

Derivative

Purine

Type

Xanthine alkaloid

Medical use

Bronchodilator

Conditions treated

Asthma, chronic bronchitis, emphysema, apnea in premature infants

Mechanism of action

Relaxes muscles in the airways for easier breathing

Administration methods

Oral, intravenous injection

Metabolism

Liver

Role

Management of respiratory conditions, improved lung function

Check Digit Verification of cas no

The CAS Registry Mumber 52083-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52083-48:
(7*5)+(6*2)+(5*0)+(4*8)+(3*3)+(2*4)+(1*8)=104
104 % 10 = 4
So 52083-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N4O4/c1-13-9-8(10(18)14(2)11(13)19)15(6-12-9)5-3-4-7(16)17/h6H,3-5H2,1-2H3,(H,16,17)/p-1

52083-48-4SDS

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 4-(1,3-dimethyl-2,6-dioxopurin-7-yl)butanoic acid

1.2 Other means of identification

Product number -
Other names 7-Theophyllinebutyricacid

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:52083-48-4 SDS

52083-48-4Downstream Products

52083-48-4Relevant academic research and scientific papers

1H NMR study of the complexation of aromatic drugs with dimethylxanthine derivatives

Hernandez Santiago,Gonzalez Flores,Rosas Castilla,Cervantes Tavera,Gutierrez Perez,Khomich,Ovchinnikov,Parkes,Evstigneev

, p. 139 - 145 (2012)

With an aim of searching efficient interceptors of aromatic drugs, the self- and hetero-association of dimethylxanthine derivatives with different structures, selected according to Strategy 1 (variation of the position of methyl groups) and Strategy 2 (variation of the length of (CH2) nCOOH group), with aromatic drug molecules: Ethidium Bromide, Proflavine and Daunomycin, were studied using 1H NMR spectroscopy. It was found that the association proceeds in a form of stacking-type complexation and its energetics is relatively independent on the structure of the dimethylxanthines. However, on average, the dimethylxanthines possess higher hetero-association constant and, hence, higher interceptor ability as compared to the trimethylxanthine, Caffeine, used during the past two decades as a typical interceptor molecule.

Antigen, antiserum and immunoassay for theophylline

-

, (2008/06/13)

By injecting a host animal with a member of a particular group of antigens [a theophylline-(7)-alkanecarboxylic acid covalently bonded to an immunogenic carrier (IGC) via the carboxyl group], antibodies, advantageously employed in determining small amounts of theophylline in biological liquids by immunoassay methods, are obtained.

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