SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.

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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

≥99.5%

Informazioni legali

产品生产厂家：巴斯夫

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

FedEx DG Service

Purezza

≥99.5%

Nomi e identificatori

Pubchem Sid

508811719

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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📊 Scheda tecnica

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

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

Slc22a6 Solute carrier family 22 member 6 (141 Activities)

Discover Target: Slc22a6

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

SARS-CoV-2 (38078 Activities)

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

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.

16 results found

Lot Number	Certificate Type	Data	Oggetto
H2621114	Certificate of Analysis	Aug 14, 2026	P301795
H2621115	Certificate of Analysis	Aug 14, 2026	P301795
H2621116	Certificate of Analysis	Aug 14, 2026	P301795
K2210338	Certificate of Analysis	Aug 04, 2026	P301795
F2520199	Certificate of Analysis	Jun 05, 2025	P301795
F2520200	Certificate of Analysis	Jun 05, 2025	P301795
F2520201	Certificate of Analysis	Jun 05, 2025	P301795
E2526036	Certificate of Analysis	Nov 01, 2022	P301795
I2425206	Certificate of Analysis	Nov 01, 2022	P301795
I2523060	Certificate of Analysis	Nov 01, 2022	P301795
K2210337	Certificate of Analysis	Nov 01, 2022	P301795
K2210354	Certificate of Analysis	Nov 01, 2022	P301795
L2423510	Certificate of Analysis	Nov 01, 2022	P301795
L2427205	Certificate of Analysis	Nov 01, 2022	P301795
L2427206	Certificate of Analysis	Nov 01, 2022	P301795
L2427215	Certificate of Analysis	Nov 01, 2022	P301795

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

Citations of This Product

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