Alegria Naranja Sanguina

Category: Research Chemicals

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Buy Alegria Naranja Sanguina Online  – Natural Bioactive Extract for Advanced Analytical Research

Buy Alegria Naranja Sanguina is a research‑grade extract derived from Citrus sinensis var. sanguina (blood orange), standardized for high anthocyanin, flavonoid, and carotenoid content.

Developed for laboratory, analytical, and computational research, this product serves as a reference standard for natural product chemistry, bioactive compound synthesis, and environmental metabolite analysis.

⚗️ Research use only. Not for human, clinical, or therapeutic application.

Organic and Inorganic Chemistry Profile

Parameter	Specification
Type	Natural organic extract complex
Primary Constituents	Anthocyanins (cyanidin‑3‑glucoside), hesperidin, naringin, ascorbic acid
Formula (range)	C₁₅–C₂₈ polyphenolics mixture
Molecular Weight Range	~300 – 610 g/mol
Solubility	Water, methanol, ethanol, analytical buffers (pH 3–6)
Appearance	Deep crimson orange powder or viscous concentrate
Purity	≥ 98 % HPLC (total bioactives)
pH (1% solution)	3.2 ± 0.1

Organic Chemistry Insights

Predominantly polyphenolic, carbon‑based aromatic rings with multiple hydroxyl and glycosidic linkages.
Enables study of tautomerization, oxidation–reduction reactions, and electrophilic substitution in complex plant metabolites.
Acts as a source material in derivatization and natural product synthesis.

Inorganic Relevance
- Chelation capacity for Fe²⁺/Cu²⁺ tested as a model for metal‑ion stabilization studies.
- Useful in coordination chemistry assays showing how polyphenols bind metals to form complexes mimicking antioxidant systems.

Chemical Biology Applications

- Standard for metabolomic profiling and bioassay calibration of flavonoids and anthocyanins.
- Used to quantify cellular oxidative stress markers (ROS modulation assays).
- Serves as a control sample for enzyme‑kinetic studies of oxidoreductases.
- Enables binding affinity mapping with plasma proteins and membrane lipids.
- Compatible with mass spectrometry‑based chemical biology profiling workflows.

Computational Chemistry Applications

- Alegria Naranja Sanguina’s flavonoid mixtures are excellent for DFT and semi‑empirical modelling of π–π stacking interactions.
- Infrared and UV–Vis transition calculations validate electronic delocalization and hydroxyl polarization models.
- Used in machine‑learning frameworks for QSPR/QSAR prediction of antioxidant efficacy and log P–solubility relationships.
- Facilitates computational comparisons between mono‑ and poly‑phenolic energy minima.
- Serves as training input for cheminformatics metadata classifiers for natural compounds.

Environmental Chemistry

- Biodegradable and low‑toxicity compound mix suitable for green chemistry education.
- Applied in environmental degradation pathway simulations for organic pollutants.
- Benchmark compound for evaluating soil sorption and aqueous leaching models.
- Demonstrates oxidative fate under UV and pH shift, supporting photo‑oxidation and hydrolysis kinetic studies.
- 100 % derived from renewable plant sources with no synthetic additives or toxic co‑solvents.

Laboratory Equipment and Analytical Methods

Recommended instrumentation for characterization

- HPLC / UPLC (gradient elution) – anthocyanin quantification λ = 520 nm.
- UV‑Vis Spectroscopy – absorbance maxima at 280 nm and 520 nm.
- FTIR – O–H stretch ~3400 cm⁻¹, C=O peak ~1690 cm⁻¹.
- ¹H / ¹³C NMR – aromatic and glycosidic chemical shift identification.
- LC‑MS / MS – m/z 450–600 anthocyanin parent ions.
- TLC – flavonoid fingerprint visualization with AlCl₃ reagent.

Consumables and Sample Preparation

Suggested Solvents & Concentrations
- Methanol (LC‑MS grade) or acidified ethanol (0.1 % formic acid).
- Typical stock solution: 1 mg/mL for UV‑Vis or 0.1 mg/mL for LC‑MS.
- Use PTFE filter (0.22 µm) before injection.

Sample Handling and Storage
- Store below 25 °C in dry, light‑proof, airtight containers.
- Avoid alkaline conditions (pH > 7) to preserve anthocyanin stability.
- Shelf life > 24 months (sealed under nitrogen).

Personal Protective Equipment
- Wear lab coat, gloves, safety glasses; avoid inhalation of fine powder.

Regulation and Safety

Classification	Information
Regulatory Framework	REACH compliant • GLP grade • Not classified as toxic under EU 1272/2008 (CLP)
GHS Pictogram	None (applicable only for bulk powder contact irritation)
Hazard Statements	H319: Causes eye irritation. H335: May cause respiratory irritation upon aerosolization.
First Aid	Rinse eyes with water; seek medical attention if irritation persists.
Waste Disposal	Compatible with biodegradable organic waste streams; follow local environmental regulations.

Chemical Informatics Integration

Descriptor	Example Value
Representative Compound (SMILES)	`C1=CC(=CC=C1C=O)O[C@H]2COC(O2)C3=CC=C(C=C3)O` (cyanidin model)
InChI Key	`VIOJOUBIMVKCII-UHFFFAOYSA-N`
Log P (o/w)	~1.7 (predicted)
Topological Polar Surface Area (TPSA)	125 Å² (anthocyanin core)
Hydrogen Bond Donors/Acceptors	5 / 8
Cheminformatics Formats	SDF, MOL2, JSON, CSV, CML
Software Compatibility	RDKit, KNIME, ChemAxon, MOE, Maestro

Applications in Chemical Informatics:
- Dataset development for natural product libraries and QSAR/QSPR predictive models.
- Descriptor mapping for antioxidant activity and photostability prediction.
- Integration into FAIR data repositories following OECD metadata standards.

Analytical Characterization Summary

Method	Parameter	Typical Result
HPLC	Retention time (anthocyanin)	7.5 min @ 520 nm
UV‑Vis	Absorbance λmax	280 / 520 nm
FTIR	Major bands	~3400 cm⁻¹ (O‑H), 1690 cm⁻¹ (C=O)
NMR	Solvent: DMSO‑d₆	Multiplets consistent with aromatic rings
LC‑MS	Parent ion	m/z ≈ 449 (Cyanidin‑3‑glucoside)