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5-Ethyl-5-(3-hydroxy-3-methylbutyl)barbituric acid is a complex organic compound belonging to the barbiturate class, characterized by its unique molecular structure. 5-Ethyl-5-(3-hydroxy-3-methylbutyl)barbituric acid is composed of a barbituric acid core, with an ethyl group at the 5-position and a 3-hydroxy-3-methylbutyl group also attached at the 5-position. The presence of the hydroxyl and methyl groups in the butyl chain contributes to its distinct chemical properties. 5-Ethyl-5-(3-hydroxy-3-methylbutyl)barbituric acid is primarily used in pharmaceutical applications, particularly as a sedative or hypnotic agent, due to its ability to depress the central nervous system. Its chemical formula is C11H20N2O4, and it exhibits specific physical and chemical characteristics that make it suitable for these medical purposes.

1421-07-4

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1421-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1421-07:
(6*1)+(5*4)+(4*2)+(3*1)+(2*0)+(1*7)=44
44 % 10 = 4
So 1421-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O4/c1-4-11(6-5-10(2,3)17)7(14)12-9(16)13-8(11)15/h17H,4-6H2,1-3H3,(H2,12,13,14,15,16)

1421-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyl-5-(3-hydroxy-3-methylbutyl)-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names Faktor I

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:1421-07-4 SDS

1421-07-4Relevant academic research and scientific papers

Relationship between polymorphism and bioavailability of amobarbital in the rabbit

Kato,Kohketsu

, p. 268 - 272 (2007/10/02)

The effect of the polymorphic form of amobarbital on its bioavailability was examined by measurement of the dissolution rate and in vivo absorption of two forms (Form I and Form II). The dissolution rate of Form II was faster than that of Form I. In in vivo absorption experiments using rabbits, two crystal forms of amobarbital were administered orally and the resulting blood time-level curves were compared with the dissolution rates. It appeared that the polymorphic form of the drug appreciably affected the absorption process from the digestive tract. Hydroxyamobarbital was confirmed to be the main metabolite of amobarbital.

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