Ammonium acetate - UltraPureChrom™, for LC-MS, ≥99% , CAS No.631-61-8

CAS: 631-61-8 Cat. No.: A112060 Formula: C₂H₇NO₂ Peso molecolare: 77.08 Beilstein Registry Number: 4186741 Numero EC: 211-162-9

QUALITÀ & PUREZZA UltraPureChrom™, for LC-MS, ≥99%

Synonyms

ammonia acetate salt | AMMONIUM ACETICUM [HPUS] | NH4OAc | DTXSID5023873 | E 264 | UNII-RRE756S6Q2 | CH3CO2NH4 | Acetic acid, ammonium salt (1:1) | E264 | E-264 | USFZMSVCRYTOJT-UHFFFAOYSA-N | AMMONIUM ACETATE | ammonium acetate- | EINECS 211-162-9 | AMMO

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Panoramica

Ammonium acetate exists as a white crystal. It is prepared from acetic acid and ammonia by neutralization to pH 7.0. It is widely used in analytical chemistry, drugs and in textile dyeing.

Specifiche

Sinonimi

ammonia acetate salt | AMMONIUM ACETICUM [HPUS] | NH4OAc | DTXSID5023873 | E 264 | UNII-RRE756S6Q2 | CH3CO2NH4 | Acetic acid, ammonium salt (1:1) | E264 | E-264 | USFZMSVCRYTOJT-UHFFFAOYSA-N | AMMONIUM ACETATE | ammonium acetate- | EINECS 211-162-9 | AMMO

Specifiche e purezza

UltraPureChrom™, for LC-MS, ≥99%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

Normal

Grado

for LC-MS, UltraPureChrom™

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

508811976

Sorrisi canonici

CC(=O)[O-].[NH4+]

IUPAC Name

azanium;acetate

InChIKey

USFZMSVCRYTOJT-UHFFFAOYSA-N

INCHI

1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3

Isomeri SMILES

CC(=O)[O-].[NH4+]

WGK Germania

1

RTECS

AF3675000

Peso molecolare

77.08

Beilstein

4186741

Reaxy-Rn

10774525

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10774525&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Organic nitrogen compounds Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: ammonium salt - acetate salt

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

Proprietà chimiche e fisiche

• Sensibilità: Miosture sensitive
• Punto di fusione (°C): 114°C
• Peso molecolare: 77.080 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 77.0477 Da
• Monoisotopic Mass: 77.0477 Da
• Topological Polar Surface Area: 41.100 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 25.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3