N,N-Dimethylglycine - 10mM in Water , CAS No.1118-68-9

CAS: 1118-68-9 Cat. No.: N420632 Peso molecular: 103.12 Beilstein Registry Number: 1700260 Número EC: 214-267-8

GRADE & PURITY 10mM in Water

Synonyms

bmse000241 | dimethylglycine | s6056 | 2-(dimethylammonio)acetate | Z235580496 | 2-(dimethylamino)acetic acid | AKOS003590893 | dimethylaminoacetic acid | dimethylamino-acetic acid | glycine, N,N-dimethyl- | N,N-dimethyglycine | N,N-Dimethylaminoacetate |

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

N,N-Dimethylglycine (DMG) is a natural N-methylated glycine that is used in comparative analysis with other N-methylated glycines such as sarcosine and βine. N,N-Dimethylglycine is used in the development of glycine-based ionic liquids and emulsifiers. N,N-Dimethylglycine is potentially useful as a biomarker of protein degradation in COPD patients. DMG is used as a substrate to identify, differentiate and characterize amino acid methyltransferase(s).

Specifications

Sinónimos

bmse000241 | dimethylglycine | s6056 | 2-(dimethylammonio)acetate | Z235580496 | 2-(dimethylamino)acetic acid | AKOS003590893 | dimethylaminoacetic acid | dimethylamino-acetic acid | glycine, N, N-dimethyl- | N, N-dimethyglycine | N, N-Dimethylaminoacetate |

Especificaciones y pureza

10mM in Water

Mecanismos bioquímicos y fisiológicos

N, N-Dimethylglycine (DMG) is a natural N-methylated glycine used in combination with other N-methylated glycines such as sarcosine and β-meso. N, N-dimethylglycine is used with For the development of glycine-based ionic liquids and emulsifiers. N, N-Dimethy

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

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Nombres e identificadores

• Sonrisas canónicas: CN(C)CC(=O)O
• IUPAC Name: 2-(dimethylamino)acetic acid
• InChIKey: FFDGPVCHZBVARC-UHFFFAOYSA-N
• INCHI: 1S/C4H9NO2/c1-5(2)3-4(6)7/h3H2,1-2H3,(H,6,7)
• Isómeros SMILES: CN(C)CC(=O)O
• WGK Alemania: 3
• RTECS: MB9865000
• CAS alternativo: 2491-06-7
• Peso molecular: 103.12
• Beilstein: 1700260
• Reaxy-Rn: 1700261
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1700261&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase 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
• Clase: 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: Trialkylamines Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid - Tertiary amine - Tertiary aliphatic amine - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
• Descripción: 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: N-methyl-amino acid - N-methylglycines

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.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 179-183 °C
• Peso molecular: 103.120 g/mol
• XLogP3: -2.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 103.063 Da
• Monoisotopic Mass: 103.063 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 70.100
• 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: 1

Referencias

1. Hongrui Yang, Chen Wang, Wenjuan Zhu, Pingning Jin, Fei Li, Jing Fan.  (2023)  A Carboxyl Group-Functionalized Ionic Liquid Hybrid Adsorbent for Solid-Phase Extraction and Determination of Trace Diclofenac Sodium in Milk Samples.  MOLECULES,  28  (17): (6216).  [PMID:37687045] [10.3390/molecules28176216]

2. Qi Zuo, Zhihui Wang, Peng Li, Luyuan Yang, Zhaozheng Song.  (2023)  Studies on the Synthesis and Application Properties of a Betaine Surfactant with a Benzene Ring Structure.  Applied Sciences-Basel,  13  (7): (4378).  [PMID:] [10.3390/app13074378]

3. Xia Qiu, Jiamin Zhang, Lilong Cao, Qin Jiao, Junhao Zhou, Lijun Yang, Hong Zhang, Yuping Wei.  (2021)  Antifouling Antioxidant Zwitterionic Dextran Hydrogels as Wound Dressing Materials with Excellent Healing Activities.  ACS Applied Materials & Interfaces,      [PMID:33543622] [10.1021/acsami.0c17744]

4. Luyao Su, Jie Mao, Sui Wang, Yufang Hu.  (2020)  A bimodal electrochemiluminescence method based on dual-enhancement Ru(bpy)32+/CQDs/AA system combined with magnetic field enhanced solid-phase microextraction for the direct determination of ascorbic acid.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2020.114376]

5. Yuhua Song, Ru Yan, Rui Dong, Ping Wen, Mingjin Fan.  (2025)  Atomic anchoring and friction-induced graphitization in nitrilotriacetate esters for customizable lubrication.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2025.129166]

6. Xiao Huang, Taisong Pan, Taiqi Hu, Runming Zeng, Siqi Chen, Jiaqi Wang, Yang Xiao, Bo Zhao, Bao Zhang, Wei Sun, Yuan Lin.  (2026)  Supramolecularly Engineered Flexible Zinc-Iodine Batteries for Wearable Electronics.  ADVANCED MATERIALS,      [PMID:41618534] [10.1002/adma.202521374]