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Calcium glycinate - 98%, high purity , CAS No.35947-07-0

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Calcium glycinate - 98%, high purity , CAS No.35947-07-0

7 Citations

COA

Grade & Purity:

≥98%

Cas Number: 35947-07-0
Molecular Weight: 188.2
PubChem CID: 10130287

In stock

Item Number

C303536

Grouped product items
SKU	Size	Availability	Price
C303536-5g	5g	2	$29.90
C303536-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$99.90
C303536-100g	100g	2	$289.90
C303536-500g	500g	1	$999.90

View related series

Amino acids (98) Calcium (4)

Basic Description

Synonyms	Calcium glycinate \| 35947-07-0 \| calcium bisglycinate \| calcium;2-aminoacetate \| Calcium glycinate (1:2) \| Glycine, Calcium Salt (2:1) \| 33242-26-1 \| 567R60Z85R \| 56960-17-9 \| Calcium 2-aminoacetate \| UNII-567R60Z85R \| calcium aminoacetate \| EINECS 251-422-9 \| EINECS 252-809-5 \| CAL
Specifications & Purity	≥98%
Storage Temp	Room temperature
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Alpha amino acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Alpha amino acids
Alternative Parents	Carboxylic acid salts Amino acids Organic calcium salts Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Not available
Substituents	Alpha-amino acid - Carboxylic acid salt - Amino acid - Organic calcium salt - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic salt - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	calcium;2-aminoacetate
INCHI	InChI=1S/2C2H5NO2.Ca/c23-1-2(4)5;/h21,3H2,(H,4,5);/q;;+2/p-2
InChIKey	OFNJDDJDXNMTHZ-UHFFFAOYSA-L
Smiles	C(C(=O)[O-])N.C(C(=O)[O-])N.[Ca+2]
Isomeric SMILES	C(C(=O)[O-])N.C(C(=O)[O-])N.[Ca+2]
Molecular Weight	188.2
Reaxy-Rn	3704066
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3704066&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number	Certificate Type	Date	Item
F2420118	Certificate of Analysis	May 28, 2024	C303536
F2420180	Certificate of Analysis	May 28, 2024	C303536
F2420181	Certificate of Analysis	May 28, 2024	C303536
F2420182	Certificate of Analysis	May 28, 2024	C303536
F2420183	Certificate of Analysis	May 28, 2024	C303536
F2420184	Certificate of Analysis	May 28, 2024	C303536
F2420185	Certificate of Analysis	May 28, 2024	C303536
F2420186	Certificate of Analysis	May 28, 2024	C303536

Chemical and Physical Properties

Molecular Weight	188.200 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	0
Exact Mass	188.011 Da
Monoisotopic Mass	188.011 Da
Topological Polar Surface Area	132.000 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	37.400
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	3

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Xijun Li, Luna Ruan, Lihua Zhu, Jun Liu, Huan Zhang. (2023) Electron synergy effect in the PtCo/CNTs bimetallic catalysts for promoting highly selective and stable hydrogenation of crotonaldehyde. MICROPOROUS AND MESOPOROUS MATERIALS, 362 (112769).
2. Xiqiang Tian, Muhammad Zahid, Jiang Li, Wang Sun, Xiaoyu Niu, Yujun Zhu. (2020) Pd/Mo2N-TiO2 as efficient catalysts for promoted selective hydrogenation of 4-nitrophenol: A green bio-reducing preparation method. JOURNAL OF CATALYSIS, 391 (190).
3. Mengting Li, Changgui Li, You Zhou, Hua Tian, Qiaoyuan Deng, Haifang Liu, Li Zhu, Xueqiong Yin. (2020) Optimization of cinnamaldehyde microcapsule wall materials by experimental and quantitative methods. JOURNAL OF APPLIED POLYMER SCIENCE, 138 (2): (49667).
4. Penghui Li, Yingyong Wang, Yunwei Wang, Guoqiang Jin, Xiang-Yun Guo, Xili Tong. (2020) Silicon Carbide Supported Palladium-Iridium Bimetallic Catalysts for Efficient Selective Hydrogenation of Cinnamaldehyde. CHINESE JOURNAL OF CHEMISTRY, 38 (4): (367-371).
5. Shiying Han, Yunfei Liu, Jiang Li, Rui Li, Fulong Yuan, Yujun Zhu. (2018) Improvement Effect of Ni to Pd-Ni/SBA-15 Catalyst for Selective Hydrogenation of Cinnamaldehyde to Hydrocinnamaldehyde. Catalysts, 8 (5): (200).
6. Zhengbin Tian, Chao Liu, Qingyang Li, Juying Hou, Yan Li, Shiyun Ai. (2015) Nitrogen- and oxygen-functionalized carbon nanotubes supported Pt-based catalyst for the selective hydrogenation of cinnamaldehyde. APPLIED CATALYSIS A-GENERAL, 506 (134).
7. Jinle Ma, Jianan Liu, Junya Zhu, Hongman Hou, Jingran Bi, Hongshun Hao, Gongliang Zhang. (2025) Synergistic antimicrobial effects of allyl isothiocyanate and cinnamaldehyde on Pseudomonas fluorescens and their application in chilled beef. LWT-FOOD SCIENCE AND TECHNOLOGY, (117447).

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