Acide propionique - AR, ≥99,5%(GC) , CAS No.79-09-4

CAS: 79-09-4 Cat. No.: P110444 Formule: C3H6O2 Poids moléculaire: 74.08 Beilstein Registry Number: 506071 Numéro CE: 201-176-3
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥99.5%(GC)
Synonyms
EPA Pesticide Chemical Code 077702 | GTPL1062 | INS NO.280 | Tox21_304030 | LMFA01010003 | acide méthylacétique | PROPIONIC-2,2-D2 ACID | Acide propionique, pour synthèse, 99,5% | ACIDE PROPIONIQUE [FCC] | Acide propionique conservateur de grains | EINECS
Storage
Room temperature
Shipped In
FedEx DG Service
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Taille
Allemagne (EU)
USA*
Prix
Qté
500ml
P110444-500ml
7 En stock
En stock ≥10

19,00€

21,61€
Enregistrer 2,60 € (12.05%)
12×500ml
P110444-12×500ml
Sur commande · 8–12 semaines

176,06€

233,34€
Enregistrer 57,27 € (24.54%)
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Pourquoi cette qualité

AR, ≥99,5%(GC) AR pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Room temperature Expédition FedEx DG Service. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 538 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

There is a slightly pungent odor. Can be miscible with water and soluble in ethanol, chloroform, and ether. Flammable. Low toxicity, median lethal dose (rat, oral) 4.29g/kg. Corrosive. Explosion limit 2.1% -12%. Determination of aromatic diamines, gas chromatography analysis standard. Insect cell culture grade is used to inhibit the growth of fungi in insect cell culture.

Spécifications

Synonymes
EPA Pesticide Chemical Code 077702 | GTPL1062 | INS NO.280 | Tox21_304030 | LMFA01010003 | acide méthylacétique | PROPIONIC-2,2-D2 ACID | Acide propionique, pour synthèse, 99,5% | ACIDE PROPIONIQUE [FCC] | Acide propionique conservateur de grains | EINECS
Spécifications et pureté
AR, ≥99,5%(GC)
Conditions de stockage de stockage
Room temperature
Expédié en
FedEx DG Service
Grade
AR
Pureté
≥99.5%(GC)
Noms et identifiants
Pubchem Sid
Sourires canoniques
CCC(=O)O
IUPAC Name
propanoic acid
InChIKey
XBDQKXXYIPTUBI-UHFFFAOYSA-N
INCHI
1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)
Isomères SMILES
CCC(=O)O
WGK Allemagne
1
RTECS
UE5950000
CAS alternatif
79-09-4,68990-37-4,68937-68-8,557-28-8 (zinc salt)
Numéro ONU
3463
Groupe d'emballage
II
Termes d'entrée MeSH
chromium propionate;ethylformic acid;lithium propanoate;Monoprop;potassium propionate;propionic acid;propionic acid, zinc salt;zinc propionate
Poids moléculaire
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=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
FFAR2 Tchem Free fatty acid receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FFAR3 Tchem Free fatty acid receptor 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR2 Tchem Free fatty acid receptor 2 (545 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLL Tbio DNA polymerase lambda (184 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FIBCD1 Tbio Fibrinogen C domain-containing protein 1 (33 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
HD1 Histone deacetylase (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a20 Solute carrier family 22 member 20 (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a6 Solute carrier family 22 member 6 (141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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Analytical Chart:

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41 results found

Lot NumberCertificate TypeDateArticle
I2624747I2624747Certificate of AnalysisSep 21, 2026 P110444
I2624746I2624746Certificate of AnalysisSep 21, 2026 P110444
G2616289G2616289Certificate of AnalysisJul 07, 2026 P110444
G2616278G2616278Certificate of AnalysisJul 07, 2026 P110444
F2611505F2611505Certificate of AnalysisJun 08, 2026 P110444
F2611499F2611499Certificate of AnalysisJun 08, 2026 P110444
F2611497F2611497Certificate of AnalysisJun 08, 2026 P110444
E2607625E2607625Certificate of AnalysisApr 27, 2026 P110444
E2607188E2607188Certificate of AnalysisApr 27, 2026 P110444
C2618596C2618596Certificate of AnalysisMar 12, 2026 P110444
C2618597C2618597Certificate of AnalysisMar 12, 2026 P110444
A2630754A2630754Certificate of AnalysisJan 21, 2026 P110444
A2630204A2630204Certificate of AnalysisJan 21, 2026 P110444
L2321387L2321387Certificate of AnalysisSep 17, 2025 P110444
D2516422D2516422Certificate of AnalysisApr 01, 2025 P110444
D2516421D2516421Certificate of AnalysisApr 01, 2025 P110444
B2520126B2520126Certificate of AnalysisDec 18, 2024 P110444
B2520127B2520127Certificate of AnalysisDec 18, 2024 P110444
K2407562K2407562Certificate of AnalysisOct 30, 2024 P110444
K2407561K2407561Certificate of AnalysisOct 30, 2024 P110444
I2402341I2402341Certificate of AnalysisAug 23, 2024 P110444
F2417199F2417199Certificate of AnalysisMay 21, 2024 P110444
F2417200F2417200Certificate of AnalysisMay 21, 2024 P110444
C2428226C2428226Certificate of AnalysisMar 22, 2024 P110444
C2428225C2428225Certificate of AnalysisMar 22, 2024 P110444
L2321381L2321381Certificate of AnalysisDec 14, 2023 P110444
G2327253G2327253Certificate of AnalysisJul 20, 2023 P110444
G2327262G2327262Certificate of AnalysisJul 20, 2023 P110444
E2329838E2329838Certificate of AnalysisMay 18, 2023 P110444
E2329848E2329848Certificate of AnalysisMay 18, 2023 P110444
D2308391D2308391Certificate of AnalysisMar 30, 2023 P110444
D2308397D2308397Certificate of AnalysisMar 30, 2023 P110444
D2323920D2323920Certificate of AnalysisMar 30, 2023 P110444
L2215943L2215943Certificate of AnalysisDec 08, 2022 P110444
L2215946L2215946Certificate of AnalysisDec 08, 2022 P110444
K2209053K2209053Certificate of AnalysisNov 01, 2022 P110444
K2209056K2209056Certificate of AnalysisNov 01, 2022 P110444
H2204421H2204421Certificate of AnalysisJul 29, 2022 P110444
H2204420H2204420Certificate of AnalysisJul 29, 2022 P110444
C2209506C2209506Certificate of AnalysisFeb 21, 2022 P110444
C2209532C2209532Certificate of AnalysisFeb 21, 2022 P110444
Propriétés chimiques et physiques
SensibilitéMoisture sensitive.
Indice de réfractionn20/D 1.386 (lit.)
Point d'éclair (°C)58℃
Point d'ébullition (°C)141.1°C
Point de fusion (°C)−24-−23 °C (lit.)
Poids moléculaire74.080 g/mol
XLogP30.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass74.0368 Da
Monoisotopic Mass74.0368 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count5
Formal Charge0
Complexity40.200
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)
Inulin: Structural Features, Physicochemical Properties, Application Development, and Research Progress in Experimental Settings
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)
Experimental Research on Candidate Probiotics: From Strain Identification and Mechanistic Evaluation to Product Selection
Why Are Preservative Systems in Daily Chemical Products Effective? Common Types, Mechanisms of Action, and Factors Affecting Preservation Efficacy
Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin
Potential Mechanisms of Succinic Acid in Acne Care: From Dicarboxylic Acid–Base Equilibria to Metabolic Antagonism Among Skin Microorganisms
Citations of This Product
Calculateurs de solution
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