Gelatin - PharmPure™, USP, BP, Ph.Eur., gel strength ~240 g Bloom , CAS No.9000-70-8

CAS: 9000-70-8 Cat. No.: G108396 EG-Nummer: 232-554-6

QUALITÄT & REINHEIT PharmPure™, USP, BP, Ph.Eur., gel strength ~240 g Bloom

Synonyms

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Storage

Room temperature,Desiccated

Shipped In

Normal

Übersicht

Gelatin is a heterogeneous mixture of water-soluble proteins of high average molecular masses, present in collagen. Proteins are extracted by boiling the relevant skin, tendons, ligaments, bones, etc. in water. Type A gelatin is derived from acid-cured tissue. Type B is derived from lime-cured tissue.
A hydrophilic chemical useful in histochemistry, bacterial culture media and light microscope autoradiography

Spezifikationen

Synonyme

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Spezifikationen & Reinheit

PharmPure™, USP, BP, Ph.Eur., gel strength ~240 g Bloom

Storage

Room temperature,Desiccated

Verschickt in

Normal

Note

BP, Ph.Eur., PharmPure™, USP

Namen und Kennungen

Pubchem Sid

508813665

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813665

Kanonisches Lächeln

CNCC(C1=CC(=C(C=C1)O)O)O.Cl

IUPAC Name

4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol;hydrochloride

InChIKey

ATADHKWKHYVBTJ-FVGYRXGTSA-N

INCHI

1S/C9H13NO3.ClH/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;/h2-4,9-13H,5H2,1H3;1H/t9-;/m0./s1

Isomere SMILES

CNC[C@@H](C1=CC(=C(C=C1)O)O)O.Cl

WGK Deutschland

3

RTECS

LX8580000

Reaxy-Rn

4019338

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4019338&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Phenols
      • Subclass Benzenediols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Phenols
• Subclass: Benzenediols
• Intermediate Tree Nodes: Not available
• Direct Parent: Catechols
• Alternative Parents: Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Secondary alcohols 1,2-aminoalcohols Dialkylamines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Monocyclic benzene moiety - 1,2-aminoalcohol - Secondary alcohol - Secondary aliphatic amine - Secondary amine - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic alcohol - Hydrochloride - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as catechols. These are compounds containing a 1,2-benzenediol moiety.
• External Descriptors: hydrochloride

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water, glycerol and acetic acid.