Gelatin - Reagent Grade , CAS No.9000-70-8

CAS: 9000-70-8 Cat. No.: G274269 Número EC: 232-554-6

GRADE & PURITY Reagent Grade

Synonyms

GINGI-PAK MAX Z-TWIST NO 2 | HY-W011910 | Adrenaline chloride | Adrenalin chloride | Epinephrine hydrochloride (JAN) | Q27107122 | GINGI-PAK MAX 2-PLY | epinephrine-hcl-adrenaline | ADRENALINE CHLORHYDRATE | GINGI-PAK MAX Z-TWIST NO 3 | Tonogen | CCRIS 23

Storage

Room temperature,Desiccated

Shipped In

Normal

Descripción general

Gelatin acts as a key element in a variety of foodstuffs and pharmaceutical products, including jellies, aspics, desserts, capsule, tablets and blood substitutes. Usually, most gelatin products have been manufactured from porcine skin.

Components

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.

Specifications

Sinónimos

GINGI-PAK MAX Z-TWIST NO 2 | HY-W011910 | Adrenaline chloride | Adrenalin chloride | Epinephrine hydrochloride (JAN) | Q27107122 | GINGI-PAK MAX 2-PLY | epinephrine-hcl-adrenaline | ADRENALINE CHLORHYDRATE | GINGI-PAK MAX Z-TWIST NO 3 | Tonogen | CCRIS 23

Especificaciones y pureza

Reagent Grade

Condiciones de almacenamiento de almacenamiento

Room temperature,Desiccated

Enviado en

Normal

Grado

Reagent Grade

Nota

A Type

Nombres e identificadores

Pubchem Sid

508813666

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813666

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