Acetate - high-purity, ≥99.8% , CAS No.64-19-7

CAS: 64-19-7 Cat. No.: A298827 Formula: CH₃CO₂H Peso molecolare: 60.05 Beilstein Registry Number: 506007 Numero EC: 200-580-7

GRADE & PURITY High-purity, ≥99.8%

Synonyms

Acetasol | Ethanoat | FEMA Number 2006 | HSDB 40 | Octowy kwas | Orthoacetic acid | Acetasol (TN) | Methanecarboxylic acid | 10.Methanecarboxylic acid | Acetic acid, ACS reagent, >=99.7% | Acido acetico [Italian] | HOOCCH3 | Acetic | Acido acetico | AI3-0

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Panoramica

Acetic acid is used in biochemical and molecular biological as a buffer when combined with sodium acetate in a specific buffering range fo pH 3.6 - 5.6. Acetic acid also is used in organic synthesis for the production of different acetates and acetyl compounds and as a precursor of polyvinylacetate and cellulose acetate.
Widely used in research and industrial uses.

Specifications

Sinonimi

Acetasol | Ethanoat | FEMA Number 2006 | HSDB 40 | Octowy kwas | Orthoacetic acid | Acetasol (TN) | Methanecarboxylic acid | 10.Methanecarboxylic acid | Acetic acid, ACS reagent, >=99.7% | Acido acetico [Italian] | HOOCCH3 | Acetic | Acido acetico | AI3-0

Specifiche e purezza

high-purity, ≥99.8%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Grado

High-purity

Purezza

≥99.8%

Nomi e identificatori

Pubchem Sid

508811888

Sorrisi canonici

CC(=O)O

IUPAC Name

acetic acid

InChIKey

QTBSBXVTEAMEQO-UHFFFAOYSA-N

INCHI

1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)

Isomeri SMILES

CC(=O)O

WGK Germania

1

RTECS

AF1225000

Numero UN

2789

Gruppo di imballaggio

II

Peso molecolare

60.05

Beilstein

506007

Reaxy-Rn

506007

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506007&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 Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - 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: Straight chain fatty acids

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

Obiettivi associati (umani)

FFAR2 Tchem Free fatty acid receptor 2 (0 Activities)

Discover Target: FFAR2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

FFAR3 Tchem Free fatty acid receptor 3 (0 Activities)

Discover Target: FFAR3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)

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FYN Tclin Tyrosine-protein kinase FYN (5308 Activities)

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HCT-116 (91556 Activities)

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FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

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FFAR2 Tchem Free fatty acid receptor 2 (545 Activities)

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POLK Tbio DNA polymerase kappa (8653 Activities)

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POLL Tbio DNA polymerase lambda (184 Activities)

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SLCO2B1 Tchem Solute carrier organic anion transporter family member 2B1 (580 Activities)

Discover Target: SLCO2B1

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water, ethanol, ether, glycerol, most organic solvents, and carbon tetrachloride. Insoluble in carbon disulfide
• Sensibilità: Moisture sensitive
• Indice di rifrazione: 1.37-1.373
• Punto di infiammabilità (°C): 40℃
• Punto di ebollizione (°C): 117-118°C
• Punto di fusione (°C): 16-16.5°C
• Peso molecolare: 60.050 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 60.0211 Da
• Monoisotopic Mass: 60.0211 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 31.000
• 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: 1