α-Hydroxyisobutyronitrile β-D-glucopyranoside
≥97% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 554-35-8
Synonym(S): α-Hydroxyisobutyronitrile β-D-glucose, 2-(β-D-Glucopyranosyloxy)-2-methylpropionitrile, Linamarin
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 MG | 68264-50-MG | In Stock | ₹ 28,004.28 |
68264 - 50 MG
In Stock
Quantity
1
Base Price: ₹ 28,004.28
GST (18%): ₹ 5,040.77
Total Price: ₹ 33,045.05
biological source
synthetic
Quality Level
100
Assay
≥97% (HPLC)
form
solid
optical activity
[α]/D -26.5±2.0°, c = 1 in H2O
technique(s)
HPLC: suitable
color
white to off-white
storage temp.
2-8°C
SMILES string
CC(C)(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C#N
InChI
1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | α-Hydroxyisobutyronitrile β-D-glucopyranoside | Sigma Aldrich | ₹ 28,004.28 | |
 | Linamarin | ChemScene | ₹ 6,844.80 - ₹ 14,545.20 | |
 | 554-35-8 | Linamarin | A2B Chem | ₹ 2,481.24 - ₹ 17,710.92 |
Related Products
Description
- Application: Linamarin, a cyanogenic glucose substrate, is used together with β-glucosidase, linamarase, to produce cyanide in vivo as a potential anticancer strategy.
- Biochem/physiol Actions: Linamarin is a cyanogenic glucoside found in the leaves and roots of plants such as cassava, lima beans, and flax. Upon exposure to enzymes and gut flora in the human intestine, linamarin and its methylated relative lotaustralin can decompose to the toxic chemical hydrogen cyanide
- Packaging: Bottomless glass bottle. Contents are inside inserted fused cone.
- 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.
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P264 - P301 + P312 - P302 + P352 - P304 + P340 + P312 - P305 + P351 + P338
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
biological source: synthetic
Quality Level: 100
Assay: ≥97% (HPLC)
form: solid
optical activity: [α]/D -26.5±2.0°, c = 1 in H2O
technique(s): HPLC: suitable
color: white to off-white
storage temp.: 2-8°C
SMILES string: CC(C)(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C#N
InChI: 1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1
biological source: __
Quality Level: 100
Assay: 96%
form: liquid
optical activity: __
technique(s): __
color: __
storage temp.: __
SMILES string: CC(C)C(=O)C1CCCCC1=O
InChI: 1S/C10H16O2/c1-7(2)10(12)8-5-3-4-6-9(8)11/h7-8H,3-6H2,1-2H3
biological source: __
Quality Level: 200
Assay: __
form: liquid
optical activity: __
technique(s): __
color: __
storage temp.: __
SMILES string: c1c[nH]cn1
InChI: 1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
