A3131
D-(−)-Arabinose
≥98% (GC)
Synonym(s):
Aldehydo-D-arabinose
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About This Item
Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
233-708-5
Beilstein/REAXYS Number:
1723079
MDL number:
biological source
synthetic (organic)
Quality Level
assay
≥98% (GC)
form
powder
optical activity
[α]20/D -105 to -103 °, c = 4% (w/v) in water
technique(s)
gas chromatography (GC): suitable
color
white to off-white
mp
162-164 °C (lit.)
solubility
water: 50 mg/mL, clear, colorless to faintly yellow
storage temp.
room temp
SMILES string
O[C@@H]1COC(O)[C@@H](O)[C@@H]1O
InChI
1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4+,5?/m1/s1
InChI key
SRBFZHDQGSBBOR-ZRMNMSDTSA-N
Application
D-(−)-Arabinose is a D-ribose analogue present in sugar polymers such as the arabinogalatans of mycobacterial cell walls and plant tissues. D-Arabinose is a substrate used to identify, differentiate and characterize arabinose isomerase(s) that have commercial value in the production of tagatose, a low calorie sweetener.
Biochem/physiol Actions
D-Arabinose is a reducing sugar. It is a pentose analog of D-ribose that is a constituent of mycobacterial cell wall arabinogalactans. It is also a substrate for D-erythroascorbic acid synthesis in yeast.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
涉药品监管产品
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Zhe Yang et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(16), 5219-5224 (2015-04-08)
Starved animals often exhibit elevated locomotion, which has been speculated to partly resemble foraging behavior and facilitate food acquisition and energy intake. Despite its importance, the neural mechanism underlying this behavior remains unknown in any species. In this study we
Derek Thomson et al.
Pulmonary pharmacology & therapeutics, 40, 69-79 (2016-05-26)
It is now recognized that certain polysaccharides can exhibit anti-inflammatory activity, including the glycosaminoglycan (GAG) heparin that is widely used as an anti-coagulant drug. However, it would be desirable to identify molecules that retain the anti-inflammatory actions of heparin, but
Nobuhiro Yamagata et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(2), 578-583 (2014-12-31)
Drosophila melanogaster can acquire a stable appetitive olfactory memory when the presentation of a sugar reward and an odor are paired. However, the neuronal mechanisms by which a single training induces long-term memory are poorly understood. Here we show that
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A3131-100G | 04061833360309 |
| A3131-1KG | 04061823686075 |
| A3131-10G | 04061833360316 |
| A3131-25G | 04061833360323 |