For anyone who wants real sweetness without the crash, the spike, or the guilt, Supercrose® delivers something the world has never had before: the full sugar experience—taste, texture, browning, mouthfeel—with demonstrably smoother metabolic behavior.
Supercrose® was engineered for people who want to enjoy food and protect their metabolic health. And for many, the biggest hesitation comes down to one question:
“If Supercrose contains glucose, won’t it spike my blood sugar?”
The answer—supported by multiple studies—is no. And here’s why.
Allulose + Glucose Behave Differently When Consumed Together
Allulose actively reduces the glycemic impact of co-ingested carbohydrates—including glucose.
Key findings:
- Allulose delays glucose absorption in the small intestine.
- Allulose improves post-meal insulin response.
- Allulose activates GLP-1 pathways naturally.
- Co-ingestion of Allulose and glucose produces a flatter glycemic curve than glucose alone.
Why Supercrose Works So Well in Baking + Cooking
Most alternative sweeteners fail in recipes. Supercrose® succeeds because it uses real sugar chemistry.
Benefits:
- Caramelizes and browns like real sugar.
- Behaves predictably under heat.
- Creates real texture and moisture retention.
- Dissolves smoothly.
- Sweetness matches real sucrose closely.
Ideal for Coffee, Tea, Smoothies & Everyday Drinks
Supercrose® dissolves instantly and tastes identical to sugar, even in cold beverages.
Advantages:
- Zero bitterness or aftertaste.
- No cooling effect.
- Supports balanced energy (glucose provides soft quick energy; Allulose blunts spikes).
- Reduced glucose excursions in beverage applications.
Why Glucose Is NOT the Enemy Here
Table sugar contains fructose—the actual metabolic problem molecule.
Supercrose® has:
- No fructose
- Glucose for functionality
- Allulose for metabolic balance
Studies show:
- Allulose reduces the metabolic load of glucose.
- Flatter blood sugar and insulin curves versus sugar.
- No fructose-driven lipogenesis or liver stress.
Perfect for People Worried About Blood Sugar or GLP-1 Medications
Allulose supports metabolic stability while glucose delivers real sugar performance.
Benefits include:
- Reduced glycemic impact vs. sugar
- Better satiety through GLP-1 activation
- No digestive irritation
- Works in all recipes without compromise
Summary: Why Supercrose Is the Future of Sweetness
Supercrose® solves two problems at once:
1) Perfect kitchen performance
2) Clinically supported metabolic advantages
You get:
- Real caramelization
- Real browning
- Real sweetness&
- Lower glycemic response
- Flatter blood sugar curves
- GLP-1 supportive benefits
- No fructose, sugar alcohols, or artificial additives
Built on science. Backed by data. Designed for real food and real metabolic health.
VIDEOS:
Sources
1. Franchi F., Yaranov L., Rollini F. et al. (2021). Effects of D-allulose on glucose tolerance and insulin response: A randomized, double-blind, crossover study. BMJ Open Diabetes Research & Care. https://pubmed.ncbi.nlm.nih.gov/33637605/
2. Tani Y., Izumori K., et al. (2023). Allulose for the attenuation of postprandial blood glucose levels: A mechanistic evaluation. PLOS ONE. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0281150
3. Au-Yeung F., et al. (2023). Comparison of postprandial glycemic and insulinemic responses to sucrose with and without allulose. Food Research International. https://www.sciencedirect.com/science/article/pii/S175646462300169X
4. Daniel H. (2022). Allulose in the human diet: The knowns and the unknowns. British Journal of Nutrition. https://www.cambridge.org/core/journals/british-journal-of-nutrition/article/allulose-in-human-diet-the-knowns-and-the-unknowns/74020152A1262DF4D7942A4DB54B6E37
5. Iwasaki Y., et al. (2018). Oral D-allulose induces GLP-1 release via intestinal sweet taste receptors and vagal activation. Nature Communications. https://www.nature.com/articles/s41467-017-02488-y
6. Cayabyab K.B., et al. (2024). The Metabolic and Endocrine Effects of a 12-Week Allulose Intervention in Adults. PubMed Central (PMC). https://pmc.ncbi.nlm.nih.gov/articles/PMC11207032/