5466-22-8 Usage
Description
Aminoacetonitrile sulfate is an organic compound that exists as a yellow to brown watery solution. It is a versatile chemical intermediate used in various industrial applications due to its unique chemical properties.
Uses
Used in Organic Synthesis:
Aminoacetonitrile sulfate is used as a building block in the synthesis of various organic compounds. Its ability to react with different reagents makes it a valuable component in creating a wide range of products.
Used as a Catalytic Agent:
In the chemical industry, Aminoacetonitrile sulfate serves as a catalyst to accelerate chemical reactions. Its presence helps increase the efficiency and speed of these reactions, leading to improved production processes and reduced costs.
Used in Petrochemical Additives:
Aminoacetonitrile sulfate is also utilized as an additive in the petrochemical industry. It plays a crucial role in enhancing the performance and quality of various petrochemical products, contributing to their overall effectiveness and reliability.
Check Digit Verification of cas no
The CAS Registry Mumber 5466-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5466-22:
(6*5)+(5*4)+(4*6)+(3*6)+(2*2)+(1*2)=98
98 % 10 = 8
So 5466-22-8 is a valid CAS Registry Number.
InChI:InChI=1/2C2H4N2.H2O4S/c2*3-1-2-4;1-5(2,3)4/h2*1,3H2;(H2,1,2,3,4)
5466-22-8Relevant articles and documents
The Ion-exchange Chromatography of Imino Derivatives of Glycine
Kawashiro, Katsuhiro,Morimoto, Shiro,Yoshida, Hideyuki
, p. 792 - 795 (2007/10/02)
The resolution of the six imino derivatives of glycine (Gly) by ion-exchange chromatography is described.The imino compounds included iminodiacetonitrile (1), iminodiacetamide (2), iminodiacetic acid (3), α-(cyanomethylamino)acetamide (4), α-(cyanomethylamino)acetic acid (5), and α-(carbamoylmethylamino)acetic acid (6).A mixture of 1-6 was chromatographed along with Gly, glycinamide, aminoacetonitrile, and NH3 with an automatic amino acid analyzer using Aminex A-4 resin column (0.25φ x 50 cm) and sodium citrate buffers.When the initial buffer of pH 3.25 was changed to pH 6.50 15 min after beginning the analysis, these ten components were completely resolved.The analysis was completed in about 4.5 h.The stability of 1, 4, and 5 in aqueous media at room temperature was also studied.