W291102

Piperonal

≥99%, FCC, FG

• Synonyme(s) : 1,3-Benzodioxole-5-carboxaldehyde, 3,4-(Methylenedioxy)benzaldehyde, Heliotropin
• Formule empirique (notation de Hill): C₈H₆O₃
• Numéro CAS: 120-57-0
• Poids moléculaire : 150.13
• Numéro FEMA: 2911
• Numéro Beilstein : 131691
• Numéro CE : 204-409-7
• Conseil de l'Europe Nº : 104
• Numéro MDL: MFCD00005828
• Code UNSPSC : 12164502
• ID de substance PubChem : 24901389
• Numéro Flavis : 5.016
• Nomenclature NACRES : NA.21

Propriétés

• Source biologique: synthetic
• Niveau de qualité: 400
• Qualité: FG; Fragrance grade; Halal; Kosher
• Agence: follows IFRA guidelines; meets purity specifications of JECFA
• Conformité réglementaire: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FCC; FDA 21 CFR 182.60
• Pression de vapeur: 1 mmHg ( 87 °C)
• Pureté: ≥99%
• Point d'ébullition: 264 °C (lit.)
• Pf: 35-39 °C (lit.)
• Application(s): flavors and fragrances
• Documentation: see Safety & Documentation for available documents
• Allergène alimentaire: no known allergens
• Allergène de parfum: heliotropine
• Propriétés organoleptiques: cherry; sweet; vanilla
• Chaîne SMILES: [H]C(=O)c1ccc2OCOc2c1
• InChI: 1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2
• Clé InChI: SATCULPHIDQDRE-UHFFFAOYSA-N

Description

Application

• 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).

Actions biochimiques/physiologiques

Taste at 10-50 ppm

Informations sur la sécurité

• Pictogrammes: GHS07
• Mention d'avertissement: Warning
• Mentions de danger: H317
• Conseils de prudence: P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
• Classification des risques: Skin Sens. 1
• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 2
• Point d'éclair (°F): 150.1 °F
• Point d'éclair (°C): 65.62 °C
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Faceshields, Gloves