توضیحات

سوکرالوز 500 گرم کمپانی گلینمارک هند
Sucralose powder
Ph Eur,ChP,NF,JPE
Agency ChP
JPE
NF
Ph. Eur.
Quality Level 500
description
form fine powder
powder
particle size ≤12 μm (d90)
pH 6-8 (20 °C, 100 g/L in H2O)
mp 130 °C (decomposition)
density 1.62 g/cm3 at 20 °C
application(s) liquid formulation
pharmaceutical
solid formulation
storage temp. 15-25°C
Application
Sucralose is a high-intensity sweetener which is non-cariogenic
and suitable for diabetics and patients with an impaired glucose
tolerance. In addition, it is readily soluble and masks both
bitterness and medicinal off-notes with equal ease – making it
exceptionally well-suited for pharmaceutical applications.
Our Sucralose is available in micronized or granular form,
both pharmaceutical grade, allowing you to choose depending
on your individual needs. Due to its optimal dispersion behavior,
sucralose powder is typically recommended for solid dose
formulations, while the fast dissolution behavior of sucralose
granular makes it very well-suited for liquid formulations..

Source Statement
The above mentioned catalog item is manufactured by chemical synthesis.
No animal or plantderived products are used in the manufacturing process.
BSE/TSE Statement
The above mentioned catalog item does not contain nor is manufactured
using any animalderived products and is therefore, BSE/TSE free.
Allergen Statement
The above mentioned catalog item does not contain any of the following:
 Milk  Cereals containing Gluten Egg  Celery Fish  Mustard Shellfish 
Sesame Seed Tree Nuts  Corn Wheat  Latex Peanuts  Sulfites > 10 ppm Soy
EU Fragrance Allergen Statement
The above mentioned catalog item does not contain any of the 26 EU
fragrance allergens listed in Annex III lines 67-92. These substances
are not intentionally added to the following chemical and therefore are not
expected to be present.
GMO Statement
The above mentioned catalog item is manufactured without the use
of genetically modified organisms and is therefore GMO free