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7214-08-6

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7214-08-6 Usage

Description

Zinc glycinate is a compound formed by the combination of zinc and glycine, an amino acid. It is known for its role in various biological processes and its ability to chelate with zinc, making it a popular choice for supplementation and various applications in different industries.

Uses

Used in Pharmaceutical Industry:
Zinc glycinate is used as a dietary supplement for its essential role in immune function, protein synthesis, and cell division. It helps maintain overall health and well-being.
Used in Cosmetics Industry:
Zinc glycinate is used as an active ingredient in skin care products for its anti-aging, acne treatment, and skin whitening properties. It is also used in the preparation of hydroxy acid complexes, which are beneficial for skin health.
Used in Food Industry:
Zinc glycinate is used as a nutrient fortifier to enhance the mineral content of various food products, contributing to better health and nutrition.
Used in Agriculture:
Zinc glycinate is utilized as a micronutrient supplement in the agricultural industry to improve crop growth, yield, and overall plant health.

Check Digit Verification of cas no

The CAS Registry Mumber 7214-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7214-08:
(6*7)+(5*2)+(4*1)+(3*4)+(2*0)+(1*8)=76
76 % 10 = 6
So 7214-08-6 is a valid CAS Registry Number.
InChI:InChI=1/2C2H5NO2.Zn/c2*3-1-2(4)5;/h2*1,3H2,(H,4,5);/q;;+2/p-2

7214-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Zinc glycinate

1.2 Other means of identification

Product number -
Other names zinc aminoacetate

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:7214-08-6 SDS

7214-08-6Synthetic route

glycine
56-40-6

glycine

zinc(II) hydroxide

zinc(II) hydroxide

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
In water at 50℃;85%
glycine
56-40-6

glycine

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
With zinc dioxide In water at 70℃; for 14h;
calcium Glycinate
33242-26-1, 35947-07-0

calcium Glycinate

A

calcium sulfate

calcium sulfate

B

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
With zinc(II) sulfate Product distribution / selectivity;
glycine
56-40-6

glycine

zinc(II) sulfate
7733-02-0

zinc(II) sulfate

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
With sodium carbonate In water at 90℃; for 0.333333h;
copper(II) glycinate
32817-15-5

copper(II) glycinate

zinc sulfide

zinc sulfide

A

copper(II) sulfide

copper(II) sulfide

B

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
In water shaken for 24 h at 25.0°C; filtration, trituration with ethanol;
glycine
56-40-6

glycine

zinc(II) oxide

zinc(II) oxide

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
With sodium glycinate In water mixing powder of ZnO and glycine in boiling water; recrystd. from sodium glycinate soln.;
zinc(II) sulfate monohydrate
100685-55-0

zinc(II) sulfate monohydrate

glycine
56-40-6

glycine

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

Conditions
ConditionsYield
With water at 28 - 57℃; for 0.466667h;
sodium glycinate
6000-44-8

sodium glycinate

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

tris(glycinato)zincate(II) ion
15841-51-7, 1141016-91-2

tris(glycinato)zincate(II) ion

Conditions
ConditionsYield
In water mixing bis(glycinato)zinc(II) and sodium glycinate in water; not isolated; detected by X-ray diffraction;
zinc(II) nitrate
10196-18-6

zinc(II) nitrate

zinc(II) glycinate
7214-08-6

zinc(II) glycinate

A

zinc(II) hexahydrate
15906-01-1

zinc(II) hexahydrate

B

tetraaquaglycinatozinc(II) ion
934182-06-6, 337967-62-1

tetraaquaglycinatozinc(II) ion

Conditions
ConditionsYield
With glycine In water dissolving crystals of bis(glycinato)zinc(II) in Zn(NO3)2 aq. soln. contg. small amt. of glycine; not isolated; detected by X-ray diffraction;

7214-08-6Downstream Products

7214-08-6Relevant articles and documents

Zinc(II) complexes with amino acids for potential use in dermatology: Synthesis, crystal structures, and antibacterial activity

Abendrot, Micha?,Ch?cińska, Lilianna,Felczak, Aleksandra,Kalinowska-Lis, Urszula,Kusz, Joachim,Lisowska, Katarzyna,Zawadzka, Katarzyna

, (2020)

The multifunctional profile of Zn2+ has influenced its great popularity in various pharmaceutical, food, and cosmetic products. Despite the use of different inorganic and organic zinc derivatives, the search for new zinc-containing compounds with a safer skin profile still remains an open issue. The present paper describes the synthesis, structural characterization, and antibacterial activity of zinc(II) complexes with proteinogenic amino acids as potential candidates for dermatological treatments. The obtained complexes are of the general formula [Zn(AA)2], where AA represents an amino acid (L-Glu, Gly, L-His, L-Pro, L-Met, and L-Trp). Their synthesis was designed in such a way that the final bis(aminoacidate) zinc(II) complexes did not contain any counter-ions such as Cl-, NO3-, or SO42- that can cause some skin irritations. The chemical structure and composition of the compounds were identified by 1H NMR spectroscopy and elemental analysis, and four were also characterized by single-crystal X-ray diffraction. The Hirshfeld surface analysis for the Zn2+ metallic center helped to determine its coordination number and geometry for each complex. Finally, the antibacterial properties of the complexes were determined with respect to three Gram-positive strains, viz. Staphylococcus aureus ATCC 6538, Staphylococcus epidermidis ATCC 12228, and Streptococcus pyogenes ATCC 19615, and two Gram-negative bacteria, viz. Escherichia coli ATCC 25992 and Pseudomonas aeruginosa ATCC 27853, and were compared with the activity of zinc 2-pirrolidone 5-carboxylate (ZnPCA), commonly applied in dermatology. It was found that the Zn(II) complexes with methionine and glycine exhibited a higher antibacterial activity than the tested standard, and the antimicrobial properties of complex with Trp were satisfactory. The results of the antimicrobial activity examination allow us to postulate that the obtained zinc complexes might become new active substances for use in dermatological products.

ENERGY-EFFICIENT SOLVENT-FREE METHOD FOR PRODUCING METAL CHELATES

-

Paragraph 0083; 0090, (2021/10/11)

The invention relates to a method for producing, amongst other things, amino-acid and/or hydroxycarboxylic-acid metal chelates, a solvent-free mixture of at least one metal oxide, metal hydroxide, metal carbonate or oxalate, and the solid organic acid is subjected to intensive mechanical stress. According to the invention, this is done in that the reaction partners are introduced in particle form into a fluid stream of a fluid-bed countercurrent mill operating without grinding elements, wherein mechanical activation of at least one of the reaction partners is effected by collision processes within a reaction chamber formed in a region of the fluid stream, and a solid body reaction to form the metal chelate is triggered. The novel method operates very energy-efficiently and with a high specific yield. It leads to a product having compact particles in the small, single-digit micrometer range having a comparatively narrow particle size distribution and a large surface. The product is homogenous and very pure. Thermal loading or decomposition of the organic chelate ligands, in particular of the amino acids, is likewise avoided, as are contaminants from milling and grinding element abrasion.

METHOD FOR THE PRODUCTION OF METAL CARBOXYLATES AND THE METAL AMINOATE OR METAL HYDROXY ANALOGUE METHIONATE DERIVATIVES THEREOF, AND USE OF SAME AS GROWTH PROMOTERS IN ANIMAL FEED

-

Page/Page column 6-7, (2008/06/13)

A method of production of metal carboxylates and of their metal carboxylate-aminoate or metal carboxylate-methioninate hydroxy analog derivatives, and their use as growth promoters in animal nutrition. It comprises mixing stoichiometric quantities of formic or butyric acid and oxide and of the dry basic salt of divalent metal, the oxide or hydroxide of Zn2+ or Cu2+, to give an exothermic reaction, without addiction of solvents, giving rise to a dry carboxylate of divalent metal that is easy to use. It also describes the use of a stage of mixing with metal aminoates or hydroxy analogs of methionine in the process, for forming either a carboxylate-aminoate of divalent metal or a carboxylate-methioninate hydroxy analog of divalent metal, products that are finally obtained in a dry form that is easy to use. Finally it describes the use of the compounds that can be obtained in the feeding of monogastric animals for improving the productivity, the bioavailability of the metals, and achieve a reduction of their emission to the environment, owing to the growth-promoting effect that they all display.

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