Ammonium lactate solution - 60 wt. % in H₂O , CAS No.515-98-0

CAS: 515-98-0 Cat. No.: A303861 Peso molecular: 107.11 Número EC: 208-214-8

GRADE & PURITY 60 wt. % in H₂O

Synonyms

Ammonium lactate [USAN] | LacHydrin | Lac-hydrin | RZOBLYBZQXQGFY-UHFFFAOYSA-N | Lactic acid ammonium salt | azanium;2-hydroxypropanoate | Propanoic acid, 2-hydroxy-, monoammonium salt, (+-)- | AMMONIUM LACTATE [MART.] | ()-Ammonium lactate; BMS 186091; L

Storage

Room temperature,Desiccated

Shipped In

Normal

Descripción general

Ammonium lactate is an ammonium salt of lactic acid. It is generally used as a feedstock for ethyl lactate and as a component of moisturizers. 

Application：

Ammonium lactate solution has been used in the ammonium lactate fermentation broth for the concentration of organic acid salts by conventional electrodialysis (EDC).

Specifications

Sinónimos

Ammonium lactate [USAN] | LacHydrin | Lac-hydrin | RZOBLYBZQXQGFY-UHFFFAOYSA-N | Lactic acid ammonium salt | azanium;2-hydroxypropanoate | Propanoic acid, 2-hydroxy-, monoammonium salt, (+-)- | AMMONIUM LACTATE [MART.] | ()-Ammonium lactate; BMS 186091; L

Especificaciones y pureza

60 wt. % in H₂O

Condiciones de almacenamiento de almacenamiento

Room temperature, Desiccated

Enviado en

Normal

Nombres e identificadores

• Sonrisas canónicas: CC(C(=O)[O-])O.[NH4+]
• IUPAC Name: azanium;2-hydroxypropanoate
• InChIKey: RZOBLYBZQXQGFY-UHFFFAOYSA-N
• INCHI: 1S/C3H6O3.H3N/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);1H3
• Isómeros SMILES: CC(C(=O)[O-])O.[NH4+]
• WGK Alemania: 3
• Peso molecular: 107.11
• Reaxy-Rn: 13648497
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13648497&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid salts
• Alternative Parents: Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic salts Organic oxides Organic nitrogen compounds Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - Carboxylic acid salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic zwitterion - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acid salts. These are ionic derivatives of carboxylic acid.
• External Descriptors: Not available

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

Propiedades químicas y físicas

• Índice de refracción: n20/D 1.363
• Peso molecular: 107.110 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 107.058 Da
• Monoisotopic Mass: 107.058 Da
• Topological Polar Surface Area: 61.400 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 53.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

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