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

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

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

Synonyms

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Storage

Room temperature,Desiccated

Shipped In

Normal

Descripción general

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

Especificaciones

Sinónimos

Gelfoam | Gelatinfoam | Galfoam | Absorbablegelatinsponge | Gelatine

Especificaciones y pureza

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

Condiciones de almacenamiento de almacenamiento

Room temperature,Desiccated

Enviado en

Normal

Grado

BP, Ph.Eur., PharmPure™, USP

Nombres e identificadores

Pubchem Sid

508813665

Pubchem Sid Url

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

Sonrisas canónicas

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

Isómeros SMILES

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

WGK Alemania

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
    • Clase Phenols
      • Subclass Benzenediols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: 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
• Descripción: 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

Mecanismos de acción

Propiedades químicas y físicas

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