Ammonium lactate solution - 10mM in DMSO , CAS No.515-98-0

CAS: 515-98-0 Cat. No.: A424432 Molecular Weight: 107.11 EC Number: 208-214-8

GRADE & PURITY 10mM in DMSO

Synonyms

Ammonium lactate|515-98-0|LacHydrin|Lac-hydrin|Ammonium (+-)-lactate|Amlactin|Laclotion|Kerasal AL|Ammonium lactate [USAN]|ammonium 2-hydroxypropanoate|Propanoic acid, 2-hydroxy-, monoammonium salt|Lac hydrin|Lactic acid ammonium salt|azanium;2-hydroxypro

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview

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

Synonyms

Ammonium lactate | 515-98-0 | LacHydrin | Lac-hydrin | Ammonium (+-)-lactate | Amlactin | Laclotion | Kerasal AL | Ammonium lactate [USAN] | ammonium 2-hydroxypropanoate | Propanoic acid, 2-hydroxy-, monoammonium salt | Lac hydrin | Lactic acid ammonium salt | azanium;2-hydroxypro

Specifications & Purity

10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

• Canonical Smiles: 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
• Isomeric SMILES: CC(C(=O)[O-])O.[NH4+]
• WGK Germany: 3
• Molecular Weight: 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
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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
• Description: 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

Chemical and Physical Properties

• Refractive Index: n20/D 1.363
• Molecular Weight: 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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