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

CAS: 9000-70-8 Cat. No.: G108396 Numero EC: 232-554-6

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

Synonyms

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Storage

Room temperature,Desiccated

Shipped In

Normal

Panoramica

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

Specifications

Sinonimi

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Specifiche e purezza

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

Condizioni di conservazione di stoccaggio

Room temperature,Desiccated

Spedito in

Normal

Grado

BP, Ph.Eur., PharmPure™, USP

Nomi e identificatori

Pubchem Sid

508813665

Pubchem Sid Url

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

Sorrisi canonici

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

Isomeri SMILES

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

WGK Germania

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
    • Classe Phenols
      • Subclass Benzenediols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Descrizione: 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

Meccanismi d'azione

Proprietà chimiche e fisiche

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