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Prova documentale

Citato in 538 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Specifiche

Sinonimi

Specifiche e purezza

ACS, ≥99.5%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

FedEx DG Service

Grado

ACS

Purezza

≥99.5%

Nomi e identificatori

Pubchem Sid

508811720

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811720

Sorrisi canonici

CCC(=O)O

IUPAC Name

propanoic acid

InChIKey

XBDQKXXYIPTUBI-UHFFFAOYSA-N

INCHI

1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)

Isomeri SMILES

CCC(=O)O

WGK Germania

RTECS

UE5950000

CAS alternativo

79-09-4,68990-37-4,68937-68-8,557-28-8 (zinc salt)

Numero UN

3463

Gruppo di imballaggio

Termini MeSH

chromium propionate;ethylformic acid;lithium propanoate;Monoprop;potassium propionate;propionic acid;propionic acid, zinc salt;zinc propionate

Peso molecolare

74.08

Beilstein

506071

Reaxy-Rn

506071

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506071&ln=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

Documento completo su pericoli, manipolazione, stoccaggio e conformità normativa.

<<<<<<< HEAD Scarica SDS → ======= Scarica SDS → >>>>>>> release248-p3

✅ Certificato di analisi (COA)

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Riepilogo di riferimento rapido delle specifiche e applicazioni del prodotto.

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🔬 Scheda delle specifiche

Attributi di qualità completi e criteri di accettazione per questa qualità.

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Dati avanzati

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
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

Struttura 3D

Obiettivi associati (umani)

FFAR2 Tchem Free fatty acid receptor 2 (0 Activities)

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

FFAR3 Tchem Free fatty acid receptor 3 (0 Activities)

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

K562 (73714 Activities)

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

HCT-116 (91556 Activities)

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SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

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FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

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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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FIBCD1 Tbio Fibrinogen C domain-containing protein 1 (33 Activities)

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Obiettivi associati (non umani)

HD1 Histone deacetylase (38 Activities)

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

Saccharomyces cerevisiae (19171 Activities)

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Candida albicans (78123 Activities)

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Mus musculus (284745 Activities)

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RAW264.7 (28094 Activities)

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Slc22a20 Solute carrier family 22 member 20 (86 Activities)

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Slc22a6 Solute carrier family 22 member 6 (141 Activities)

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SARS-CoV-2 (38078 Activities)

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Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot Number	Certificate Type	Data	Oggetto
G2609149	Certificate of Analysis	Apr 06, 2026	P110447
C2613059	Certificate of Analysis	Apr 06, 2026	P110447
H2526086	Certificate of Analysis	Sep 06, 2025	P110447
B2605060	Certificate of Analysis	Sep 03, 2025	P110447
H2526088	Certificate of Analysis	Sep 03, 2025	P110447
H2526087	Certificate of Analysis	Sep 02, 2025	P110447
H2522157	Certificate of Analysis	Aug 08, 2024	P110447
I2404419	Certificate of Analysis	Aug 08, 2024	P110447
I2404434	Certificate of Analysis	Aug 08, 2024	P110447
I2404435	Certificate of Analysis	Aug 08, 2024	P110447
C2609084	Certificate of Analysis	Oct 24, 2023	P110447
A2417082	Certificate of Analysis	Oct 24, 2023	P110447
K2313395	Certificate of Analysis	Oct 24, 2023	P110447
K2313459	Certificate of Analysis	Oct 24, 2023	P110447
K2313486	Certificate of Analysis	Oct 24, 2023	P110447
K2209046	Certificate of Analysis	Nov 17, 2022	P110447
J2215157	Certificate of Analysis	Oct 18, 2022	P110447
C2209519	Certificate of Analysis	Mar 14, 2022	P110447

Proprietà chimiche e fisiche

Sensibilità	Moisture sensitive.
Indice di rifrazione	n20/D 1.386 (lit.)
Punto di infiammabilità (°C)	58℃
Punto di ebollizione (°C)	141.1°C
Punto di fusione (°C)	−24-−23 °C (lit.)
Peso molecolare	74.080 g/mol
XLogP3	0.300
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	74.0368 Da
Monoisotopic Mass	74.0368 Da
Topological Polar Surface Area	37.300 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	40.200
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

Domande frequenti e articoli

Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Fatty acids Long-chain carbon compounds

Inulin: Structural Features, Physicochemical Properties, Application Development, and Research Progress in Experimental Settings

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Inulin Fructan Soluble dietary fiber Prebiotic Degree of polymerization Short-chain fatty acids Inulin clearance

How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pharmaceuticals Organic Acids

Experimental Research on Candidate Probiotics: From Strain Identification and Mechanistic Evaluation to Product Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Probiotics Microorganism Strain specificity

Why Are Preservative Systems in Daily Chemical Products Effective? Common Types, Mechanisms of Action, and Factors Affecting Preservation Efficacy

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Preservatives

Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

skin care Probiotics

Potential Mechanisms of Succinic Acid in Acne Care: From Dicarboxylic Acid–Base Equilibria to Metabolic Antagonism Among Skin Microorganisms

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Succinic Acid Acne

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