F9048
D-(−)-Fructose
98.0-102.0% dry basis, meets USP testing specifications
Sinónimos:
D-Levulose, Fruit sugar
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Fórmula empírica (notación de Hill):
C6H12O6
Número CAS:
Peso molecular:
180.16
UNSPSC Code:
12352201
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-333-3
Beilstein/REAXYS Number:
1239004
MDL number:
Servicio técnico
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Permítanos ayudarlebiological source
natural (organic)
Quality Level
agency
USP/NF, meets USP testing specifications
assay
98.0-102.0% dry basis
form
crystalline
impurities
<0.018% chloride content, <0.025% sulphate
color
colorless
useful pH range
5.0-7 (25 °C, 18 g/L)
mp
119-122 °C (dec.) (lit.)
solubility
water: 790 g/L at 20 °C
cation traces
Ca: ≤0.005%, Mg: ≤0.005%
application(s)
pharmaceutical (small molecule)
storage temp.
room temp
SMILES string
OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO
InChI
1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5-,6-/m1/s1
InChI key
BJHIKXHVCXFQLS-UYFOZJQFSA-N
Application
- Identification of hyperthermophilic D-allulose 3-epimerase from Thermotoga sp. and its application as a high-performance biocatalyst for D-allulose synthesis: This research highlights the application of D-(−)-Fructose in the biocatalytic synthesis of D-allulose, emphasizing its potential in the production of low-calorie sweeteners in pharmaceutical formulations (Shen et al., 2024).
- Staphylococcus hsinchuensis sp. nov., Isolated from Soymilk: In this study, D-(−)-Fructose is utilized in the media for culturing and identifying new microbial species, underscoring its role in microbiological research within biotechnological and pharmaceutical fields (Wang et al., 2024).
Other Notes
To gain a comprehensive understanding of our extensive range of Oligosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Clase de almacenamiento
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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