Gelatina - Grau de reagente , CAS No.9000-70-8

CAS: 9000-70-8 Cat. No.: G274269 Número CE: 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

Temperatura ambiente

Shipped In

Normal

Visão geral

Introdução ao produto

A gelatina actua como um elemento-chave numa variedade de géneros alimentícios e produtos farmacêuticos, incluindo geleias, aspics, sobremesas, cápsulas, comprimidos e substitutos do sangue. Normalmente, a maioria dos produtos de gelatina é fabricada a partir de pele de suíno.

Componentes

A gelatina é uma mistura heterogénea de proteínas hidrossolúveis de massas moleculares médias elevadas, presentes no colagénio. As proteínas são extraídas através da fervura da pele, tendões, ligamentos, ossos, etc. em água. A gelatina de tipo A é derivada de tecido curado com ácido. O tipo B é derivado de tecido curado com cal.

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

Especificações e pureza

Grau de reagente

Condições de armazenamento de armazenamento

Temperatura ambiente

Enviado em

Normal

Grau

Reagent Grade

Nota

tipo B (sangue, gripe, hepatite, etc.)

Nomes e identificadores

Pubchem Sid

508813666

Pubchem Sid Url

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

Sorrisos canónicos

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

SMILES isoméricas

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

WGK Alemanha

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
• Descrição: 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 ação