dextran sulfates - 100 kDa LS , CAS No.9011-18-1

CAS: 9011-18-1 Cat. No.: D397464 Numéro CE: 618-471-1 PubChem CID: 2337

QUALITÉ & PURETÉ 100 kDa LS

Synonyms

4-aminobenzoic acid-ethyl ester | Anaesthesinum | Benzoak | ETHYL4-AMINOBENZOATE | Norcaine | Norcainum | Aethoform | Anaesthin | Bensokain | HSDB 7225 | BENZOCAINE [USP MONOGRAPH] | CAS-94-09-7 | Benzoic acid, 4-amino-, ethyl ester | Chiggerex | Ethoform

Storage

Store at 2-8°C,Argon charged,Desiccated

Shipped In

Wet ice

Vue d’ensemble

Product Description：

Dextran sulfates are produced by sulfation of selected dextran fractions.

The dextran sulfate is supplied as the sodium salt and is stabilised by a small addition of phosphate salts. A certificate of analysis is supplied with each batch. The molecular weight range, sulfur content, moisture etc. are carefully controlled.

Structure

Dextran is a polysaccharide derived from the bacterium Leuconostoc mesenteroides B512F and consists of an α-D-(1 – 6) linear glucan with a low content (ca. 5%) of sidechains linked to the 3-carbon of glucose. Dextran sulfate is a sulfated derivative of selected dextran fraction. The sulfate content of our low sulfated dextran sulfates lies between 8 to 13 %.

Applications

Dextran sulfate have a wide range of applications areas and properties. Some examples are:

Anti-coagulation agent in cell media

Selective precipitation of lipoproteins

Acceleration of DNA hybridisation.

Releasing DNA from DNA-histones complexes

Inhibition tRNA-binding to ribosomes

Inhibition of ribonucleases

Anti-viral properties

Used in cosmetics for anti-inflammation properties and osmotic retention of water

Separation of microorganisms and macromolecules

Adjuvant in vaccines

Studies of perm selectivity of membranes

Spécifications

Synonymes

4-aminobenzoic acid-ethyl ester | Anaesthesinum | Benzoak | ETHYL4-AMINOBENZOATE | Norcaine | Norcainum | Aethoform | Anaesthin | Bensokain | HSDB 7225 | BENZOCAINE [USP MONOGRAPH] | CAS-94-09-7 | Benzoic acid, 4-amino-, ethyl ester | Chiggerex | Ethoform

Spécifications et pureté

100 kDa LS

Conditions de stockage de stockage

Store at 2-8°C,Argon charged,Desiccated

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Propriétés du produit

ALogP

1.9

Noms et identifiants

IUPAC Name

ethyl 4-aminobenzoate

InChIKey

BLFLLBZGZJTVJG-UHFFFAOYSA-N

INCHI

1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3

Isomères SMILES

CCOC(=O)C1=CC=C(C=C1)N

WGK Allemagne

2

RTECS

HH9290000

PubChem CID

2337

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoic acid esters
• Alternative Parents: Aminobenzoic acids and derivatives Benzoyl derivatives Aniline and substituted anilines Carboxylic acid esters Amino acids and derivatives Monocarboxylic acids and derivatives Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aminobenzoic acid or derivatives - Benzoate ester - Benzoyl - Aniline or substituted anilines - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
• External Descriptors: substituted aniline - benzoate ester

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

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: readily soluble in water
• Sensibilité: Moisture sensitive
• Rotation spécifique [α]: 93° (C=6,H2O)
• Poids moléculaire: 165.190 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 165.079 Da
• Monoisotopic Mass: 165.079 Da
• Topological Polar Surface Area: 52.300 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 151.000
• 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