Sarcosine - UltraBio™, Ultra pure , CAS No.107-97-1

CAS: 107-97-1 Cat. No.: S431365 Formula: C₃H₇NO₂ Peso molecolare: 89.09 Beilstein Registry Number: 4345 Numero EC: 203-538-6 PubChem CID: 1088

QUALITÀ & PUREZZA UltraBio™, Ultra pure

Synonyms

GTPL4713 | N-Cocoyl sarcosine | (Methylamino)ethanoic acid | Me-Gly-OH | (methylamino)acetate | (methylamino)-Acetate | N-Cocoyl-N-methylglycine | sarcosinate | 2-Methylaminoethanoic acid | DTXSID1047025 | CH3NHCH2COOH | BBL009707 | MeGly | AC7804 | CH3NH

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifiche

Sinonimi

GTPL4713 | N-Cocoyl sarcosine | (Methylamino)ethanoic acid | Me-Gly-OH | (methylamino)acetate | (methylamino)-Acetate | N-Cocoyl-N-methylglycine | sarcosinate | 2-Methylaminoethanoic acid | DTXSID1047025 | CH3NHCH2COOH | BBL009707 | MeGly | AC7804 | CH3NH

Specifiche e purezza

UltraBio™, Ultra pure

Condizioni di conservazione di stoccaggio

Room temperature,Desiccated

Spedito in

Normal

Grado

Ultra pure, UltraBio™

Nomi e identificatori

Pubchem Sid

528774929

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528774929

Sorrisi canonici

CNCC(=O)O

IUPAC Name

2-(methylamino)acetic acid

InChIKey

FSYKKLYZXJSNPZ-UHFFFAOYSA-N

INCHI

1S/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6)

Isomeri SMILES

CNCC(=O)O

WGK Germania

1

RTECS

VQ2897000

PubChem CID

1088

Peso molecolare

89.09

Beilstein

4345

Reaxy-Rn

1699442

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe 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
• Classe: 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: Amino acids Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid - Amino acid - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
• Descrizione: 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-alkylglycine - 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

Obiettivi associati (umani)

POLI Tchem DNA polymerase iota (116820 Activities)

Discover Target: POLI

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)

Discover Target: SLC36A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TARDBP Tchem TAR DNA-binding protein 43 (40113 Activities)

Discover Target: TARDBP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

ampC Beta-lactamase AmpC (62480 Activities)

Discover Target: ampC

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc6a9 Glycine transporter 1 (255 Activities)

Discover Target: Slc6a9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: H2O: 1M, clear, colorless
• Sensibilità: Moisture sensitive
• Punto di fusione (°C): 208-212°C
• Peso molecolare: 89.090 g/mol
• XLogP3: -2.800
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 89.0477 Da
• Monoisotopic Mass: 89.0477 Da
• Topological Polar Surface Area: 49.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 52.800
• 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