SODIUM GLYCINATE

Base Information

• Chemical Name: SODIUM GLYCINATE
• CAS No.: 6000-44-8
• Molecular Formula: C2H4NNaO2
• Molecular Weight: 97.049
• Hs Code.: 2922.49 Oral rat LD50 7930 mg/kg
• Mol file: 6000-44-8.mol

Synonyms:Glycine,monosodium salt (8CI,9CI);Glycine sodium;Glycine sodium salt;Sodiumaminoacetate;Sodium glycinate;Sodium glycine;Sodium glycocollate;

Chemical Property of SODIUM GLYCINATE

Chemical Property:

• Appearance/Colour: white to off-white crystalline powder
• Vapor Pressure: 5.55E-05mmHg at 25°C
• Melting Point: 290oC decomposes
• Refractive Index: 1.491
• Boiling Point: 240.9 °C at 760 mmHg
• PKA: 4.3[at 20 ℃]
• Flash Point: 99.5 °C
• PSA: 66.15000
• Density: 1.014g/cm3
• LogP: -1.60470
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 98.02179768
• Heavy Atom Count: 6
• Complexity: 42.9

Purity/Quality:

99% ^*data from raw suppliers

SodumGlycinate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C(=O)O)N.[Na]
• Description: Sodium glycinate is a non-essential amino acid. It is found primarily in gelatin and silk fibroin and used therapeutically as a nutrient. It is also a fast inhibitory neurotransmitter.
• Uses: Sodum glycinate is a useful research chemical. It Inhibits spinal cord neurotransmitter, allosteric regulator of NMDA receptors.

Technology Process of SODIUM GLYCINATE

There total 10 articles about SODIUM GLYCINATE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

glycine (56-40-6,18875-39-3,25718-94-9) → sodium glycinate (6000-44-8)

Guidance literature:

With sodium hydroxide; In glycerol; at 120 ℃; for 1h;

Reference yield: 96.7%

(2-hydroxyethyl)(methyl)amine (109-83-1) → sodium glycinate (6000-44-8)

Guidance literature:

With sodium hydroxide; Pd-doped copper catalyst on active carbon; In water; at 160 ℃; under 9000.9 Torr;

Reference yield:

ethanolamine (141-43-5) → sodium glycinate (6000-44-8)

Guidance literature:

With sodium hydroxide; oxygen; Au-Ir/ZrO₂; In water; at 110 ℃; for 3h; under 7500.75 Torr; Product distribution / selectivity;

upstream raw materials:

glycine

Sodium; ((Z)-2-ethoxycarbonyl-1-methyl-vinylamino)-acetate

ethanolamine

zirconyl chloride

Downstream raw materials:

2-[(Benzyloxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-pent-4-enoic acid ethyl ester

N-stearoylglycine

N-myristoylglycine

[6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydrofuran-2-yl)-9H-purin-8-ylamino]-acetic acid

Refernces

• 1、 Gao, Sheng,Gong, Xinjian,Lu, Zaijun,Song, Kun,Wang, Zheng,Yao, Shu,Zhang, Sujuan. "A bio-based benzoxazine surfactant from amino acids". . p. 3481 - 3488. Retrieved 2020.
• 2、 -. "MANUFACTURING METHOD OF AMINOCARBOXYLIC ACID SALT". Paragraph 0076. . Retrieved 2017/06/15.