W291102

Piperonal

≥99%, FCC, FG

• Synonym(e): 3,4-Methylendioxy-benzaldehyd, Heliotropin
• Empirische Formel (Hill-System): C₈H₆O₃
• CAS-Nummer: 120-57-0
• Molekulargewicht: 150.13
• FEMA-Nummer: 2911
• Beilstein: 131691
• EG-Nummer: 204-409-7
• CoE-Nummer: 104
• MDL-Nummer: MFCD00005828
• UNSPSC-Code: 12164502
• PubChem Substanz-ID: 24901389
• Flavis-Nummer: 5.016
• NACRES: NA.21
• Organoleptisch: cherry; sweet; vanilla
• Qualität: FG; Fragrance grade; Halal; Kosher
• Biologische Quelle: synthetic
• Agentur: follows IFRA guidelines; meets purity specifications of JECFA
• Nahrungsmittelallergen: no known allergens

Eigenschaften

• Biologische Quelle: synthetic
• Qualitätsniveau: 400
• Qualität: FG; Fragrance grade; Halal; Kosher
• Agentur: follows IFRA guidelines; meets purity specifications of JECFA
• Einhaltung gesetzlicher Vorschriften: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FCC; FDA 21 CFR 182.60
• Dampfdruck: 1 mmHg ( 87 °C)
• Assay: ≥99%
• bp: 264 °C (lit.)
• mp (Schmelzpunkt): 35-39 °C (lit.)
• Anwendung(en): flavors and fragrances
• Dokumentation: see Safety & Documentation for available documents
• Nahrungsmittelallergen: no known allergens
• Allergener Duftstoff: heliotropine
• Organoleptisch: cherry; sweet; vanilla
• SMILES String: [H]C(=O)c1ccc2OCOc2c1
• InChI: 1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2
• InChIKey: SATCULPHIDQDRE-UHFFFAOYSA-N

Beschreibung

Anwendung

• The synthesis and characterisation of MDMA derived from a catalytic oxidation of material isolated from black pepper reveals potential route specific impurities.: This study explores the synthesis and characterization of MDMA from piperonal, highlighting potential impurities unique to this synthesis route. This research has implications for forensic science and the identification of synthetic routes for MDMA (Plummer et al., 2016).


• Design, synthesis, and biological evaluation of platensimycin analogues with varying degrees of molecular complexity.: This paper details the synthesis of platensimycin analogues using piperonal derivatives. The study evaluates the biological activities of these analogues, contributing to the development of new antibacterial agents (Nicolaou et al., 2008).


• Synthesis and use of 4-peptidylhydrazido-N-hexyl-1,8-naphthalimides as fluorogenic histochemical substrates for dipeptidyl peptidase IV and tripeptidyl peptidase I.: This research presents the synthesis of piperonal-based substrates for histochemical applications, enabling the study of enzyme activities in biochemical assays (Ivanov et al., 2009).

Biochem./physiol. Wirkung

Taste at 10-50 ppm

Sicherheitshinweise

• Piktogramme: GHS07
• Signalwort: Warning
• H-Sätze: H317
• P-Sätze: P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
• Gefahreneinstufungen: Skin Sens. 1
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 2
• Flammpunkt (°F): 150.1 °F
• Flammpunkt (°C): 65.62 °C
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Faceshields, Gloves