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L-Methionine-(methyl-d3) - 98 atom % D, high purity , CAS No.13010-53-2
Basic Description
Synonyms
L-Methionine-methyl-D3 | l-Methionine-d3 | 13010-53-2 | L-Methionine-(methyl-d3) | (2S)-2-amino-4-(trideuteriomethylsulfanyl)butanoic acid | Cymethion-d3 | L-Methionine-d3 (S-methyl-d3) | L-(~2~H_3_)Methionine | (S)-2-Amino-4-(methylthio-d3)butanoic Acid | DTXSID90574088 | C
Specifications & Purity
≥98 atom% D
Storage Temp
Protected from light
Shipped In
Normal
Product Description
L-Methionine-d3 is labelled L-Methionine, an essential amino acid for human development. Hepatoprotectant; antidote (acetominophen poisoning); urinary acidifier.
Taxonomic Classification
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
Methionine and derivatives
Alternative Parents
L-alpha-amino acids Thia fatty acids Amino acids Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Methionine or derivatives - Alpha-amino acid - L-alpha-amino acid - Thia fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Organic oxygen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors
Not available
Data sources
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.
Names and Identifiers
Pubchem Sid
488198917
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488198917
IUPAC Name
(2S)-2-amino-4-(trideuteriomethylsulfanyl)butanoic acid
INCHI
InChI=1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1/i1D3
InChIKey
FFEARJCKVFRZRR-OSIBIXDNSA-N
Smiles
CSCCC(C(=O)O)N
Isomeric SMILES
[2H]C([2H])([2H])SCC[C@@H](C(=O)O)N
Molecular Weight
152.23
Reaxy-Rn
636185
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636185&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water
Sensitivity
Air & Moisture & Light sensitive
Melt Point(°C)
284 °C
Molecular Weight
152.230 g/mol
XLogP3
-1.900
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
4
Exact Mass
152.07 Da
Monoisotopic Mass
152.07 Da
Topological Polar Surface Area
88.600 Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
97.000
Isotope Atom Count
3
Defined Atom Stereocenter Count
1
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
1
Citations of This Product
1.
You Xue-Jiao, Zhang Shan, Chen Juan-Juan, Tang Feng, He Jingang, Wang Jie, Qi Chu-Bo, Feng Yu-Qi, Yuan Bi-Feng.
(2022)
Formation and removal of 1,N6-dimethyladenosine in mammalian transfer RNA. NUCLEIC ACIDS RESEARCH,
50
(17):
(9858-9872).
2.
Qing-Yun Cheng, Jun Xiong, Cheng-Jie Ma, Yi Dai, Jiang-Hui Ding, Fei-Long Liu, Bi-Feng Yuan, Yu-Qi Feng.
(2020)
Chemical tagging for sensitive determination of uridine modifications in RNA. Chemical Science,
11
(7):
(1878-1891).
3.
Zhijian Zha, Ruihua Wang, Qian Wang, Fahui Chen, Ziyang Ye, Yafeng Li.
(2024)
A fast and efficient liquid chromatography–tandem mass spectrometry method for measuring l- and d-amino acids in the urine of patients with immunoglobulin A nephropathy. BIOMEDICAL CHROMATOGRAPHY,
38
(6):
(e5866).
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3 Citations
C23021082