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Piperonal

ALDRICH/W291102 - ≥99%, FCC, FG

Synonym: 1,3-Benzodioxole-5-carboxaldehyde; 3,4-(Methylenedioxy)benzaldehyde; Heliotropin

CAS Number: 120-57-0
Empirical Formula (Hill Notation): C8H6O3
Molecular Weight: 150.13
EC Number: 204-409-7
MDL Number: MFCD00005828
Linear Formula: C8H6O3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-W291102-1KG-K 1 kg
$129.00
1/EA
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45-W291102-10KG-K 10 kg
$0.00
1/EA
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45-W291102-25KG-K 25 kg
$0.00
1/EA
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45-W291102-50KG-K 50 kg
$0.00
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45-W291102-SAMPLE-K
$54.60
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agency follows IFRA guidelines
  meets purity specifications of JECFA
application(s) flavors and fragrances
assay ≥99%
biological source synthetic
bp 264 °C (lit.)
documentation see Safety & Documentation for available documents
food allergen no known allergens
fragrance allergen heliotropine
grade FG
  Fragrance grade
  Halal
  Kosher
InChI 1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2
InChI key SATCULPHIDQDRE-UHFFFAOYSA-N
mp 35-39 °C (lit.)
organoleptic cherry; sweet; vanilla
Quality Level 400 
reg. compliance EU Regulation 1223/2009
  EU Regulation 1334/2008 & 178/2002
  FCC
  FDA 21 CFR 182.60
SMILES string [H]C(=O)c1ccc2OCOc2c1
vapor pressure 1 mmHg ( 87 °C)
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 ).

Biochem/physiol Actions: Taste at 10-50 ppm
Packaging: 1 kg in poly bottle
Packaging: 10 kg in poly drum
Packaging: 25, 50 kg in fiber drum
Purity ≥99%
bp 264 °C (lit.)
mp 35-39 °C (lit.)
FEMA Number 2911
UNSPSC 12164502

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