Acrylic acid - ≥95% , CAS No.79-10-7

CAS: 79-10-7 Cat. No.: A615488 Formule: C₃H₄O₂ Poids moléculaire: 72.06 Beilstein Registry Number: 635743 Numéro CE: 201-177-9

QUALITÉ & PURETÉ ≥95%

Synonyms

ACRYLIC ACID|2-Propenoic acid|79-10-7|prop-2-enoic acid|Vinylformic acid|Propenoic acid|Acroleic acid|Ethylenecarboxylic acid|Propene acid|ACRYLATE|Propenoate|Glacial acrylic acid|Kyselina akrylova|Acrylic acid, glacial|9003-01-4|RCRA waste number U008|Ac

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

Vue d’ensemble

Usually used in preparing monodispersed poly (N-isopropylacryamide) (PNIPAM)/AAc microgels.And also used primarily as an intermediate in the production of acrylates.

Spécifications

Synonymes

ACRYLIC ACID | 2-Propenoic acid | 79-10-7 | prop-2-enoic acid | Vinylformic acid | Propenoic acid | Acroleic acid | Ethylenecarboxylic acid | Propene acid | ACRYLATE | Propenoate | Glacial acrylic acid | Kyselina akrylova | Acrylic acid, glacial | 9003-01-4 | RCRA waste number U008 | Ac

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Protected from light,Room temperature,Argon charged

Expédié en

FedEx DG Service

Pureté

≥95%

Product Line

A615488-500g

Noms et identifiants

Pubchem Sid

508811677

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811677

Sourires canoniques

C=CC(=O)O

IUPAC Name

prop-2-enoic acid

InChIKey

NIXOWILDQLNWCW-UHFFFAOYSA-N

INCHI

1S/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)

Isomères SMILES

C=CC(=O)O

WGK Allemagne

1

RTECS

AS4375000

Numéro ONU

2218

Groupe d'emballage

II

Poids moléculaire

72.06

Beilstein

635743

Reaxy-Rn

635743

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635743&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as acrylic acids. These are organic compounds containing acrylic acid CH2=CHCO2H.
• External Descriptors: Unsaturated 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

Cibles associées (humaines)

CHAT Tchem Choline acetylase (63 Activities)

Discover Target: CHAT

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water, chloroform, ethanol, methanol, and DMF.
• Sensibilité: Hygroscopic,Light & Air sensitive.
• Indice de réfraction: 1.4192-1.4212
• Point d'éclair (°F): 119.3 °F - closed cup
• Point d'éclair (°C): 48.5 °C - closed cup
• Point d'ébullition (°C): 139°C
• Point de fusion (°C): 13°C
• Poids moléculaire: 72.060 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 72.0211 Da
• Monoisotopic Mass: 72.0211 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 55.900
• 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

Foire aux questions

What is the purity of this product?

This product is supplied at ≥95% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 79-10-7, the molecular formula is C3H4O2 , and the molecular weight is 72.06 g/mol. InChIKey NIXOWILDQLNWCW-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.