94258
Eriodictyol
≥95.0% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 4049-38-1
Synonym(S): 3′,4′,5,7-Tetrahydroxyflavanone
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 MG | 94258-5-MG | In Stock | ₹ 16,518.95 |
94258 - 5 MG
In Stock
Quantity
1
Base Price: ₹ 16,518.95
GST (18%): ₹ 2,973.411
Total Price: ₹ 19,492.361
Quality Level
100
Assay
≥95.0% (HPLC)
form
powder
application(s)
metabolomicsvitamins, nutraceuticals, and natural products
storage temp.
−20°C
SMILES string
O=C1C2=C(O)C=C(O)C=C2OC(C3=CC=C(O)C(O)=C3)C1
InChI
1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2
InChI key
SBHXYTNGIZCORC-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Eriodictyol | Sigma Aldrich | ₹ 36,772.53 | |
 | Eriodictyol | Aaron Chemicals LLC | ₹ 3,679.08 - ₹ 6,245.88 | |
 | 4049-38-1 | Eriodictyol | A2B Chem | ₹ 3,507.96 |
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Description
- General description: Eriodictyolis a bitter-masking dietary flavonoid primarily extracted from yerba Santa Clause (Eriodictyon californicum) and Dracocephalum rupestre, but also present in many other citrus fruits, medicinal plants, and vegetables.
- Application: Eriodictyolmay has been used to study its mechanism on IgE/Ag-induced type I hypersensitivity inhibition at the level of mast cell degranulation and ceramide kinase activity. It may also be used to understand its potential antidiabetic activity and its neuroprotective activity via activation of the Nrf2/ARE signaling pathway.
- Biochem/physiol Actions: Eriodictyolis absorbed in the body slowly and can be found in plasma and urine as homoeriodictyol, a conjugated form. It has many pharmacological properties such as antioxidant, anti-inflammatory, anti-cancer, anti-diabetic, anti-obesity, neuroprotective, cardioprotective, and hepatoprotective.
- Packaging: Bottomless glass bottle. Contents are inside inserted fused cone.
- Other Notes: For this product we use the non-stereospecific CAS number. It is expected that the natural enantiomer is predominant, however the substance is prone to racemization in solution. The product is therefore not specified stereospecifically and is only recommended to be used for non-stereospecific analysis.
SAFETY INFORMATION
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Quality Level: 100
Assay: ≥95.0% (HPLC)
form: powder
application(s): metabolomicsvitamins, nutraceuticals, and natural products
storage temp.: −20°C
SMILES string: O=C1C2=C(O)C=C(O)C=C2OC(C3=CC=C(O)C(O)=C3)C1
InChI: 1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2
InChI key: SBHXYTNGIZCORC-UHFFFAOYSA-N
Quality Level:
100
Assay:
≥95.0% (HPLC)
form:
powder
application(s):
metabolomicsvitamins, nutraceuticals, and natural products
storage temp.:
−20°C
SMILES string:
O=C1C2=C(O)C=C(O)C=C2OC(C3=CC=C(O)C(O)=C3)C1
InChI:
1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2
InChI key:
SBHXYTNGIZCORC-UHFFFAOYSA-N
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storage temp.: −20°C
SMILES string: [Li+].[Li+].[Li+].[Li+].CC(O)(CCOP([O-])(=O)OP([O-])([O-])=O)CC([O-])=O
InChI: 1S/C6H14O10P2.4Li/c1-6(9,4-5(7)8)2-3-15-18(13,14)16-17(10,11)12;;;;/h9H,2-4H2,1H3,(H,7,8)(H,13,14)(H2,10,11,12);;;;/q;4*+1/p-4
InChI key: GFIXUUFXTAPBAD-UHFFFAOYSA-J
Quality Level:
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≥80% (qNMR)
form:
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storage temp.:
−20°C
SMILES string:
[Li+].[Li+].[Li+].[Li+].CC(O)(CCOP([O-])(=O)OP([O-])([O-])=O)CC([O-])=O
InChI:
1S/C6H14O10P2.4Li/c1-6(9,4-5(7)8)2-3-15-18(13,14)16-17(10,11)12;;;;/h9H,2-4H2,1H3,(H,7,8)(H,13,14)(H2,10,11,12);;;;/q;4*+1/p-4
InChI key:
GFIXUUFXTAPBAD-UHFFFAOYSA-J
Quality Level: 200
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powder (Lyophilisate)
application(s):
__
storage temp.:
−20°C
SMILES string:
__
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__
InChI key:
__
Quality Level: 200
Assay: ≥95% (HPLC)
form: powder (Lyophilisate)
application(s): __
storage temp.: −20°C
SMILES string: __
InChI: __
InChI key: __
Quality Level:
200
Assay:
≥95% (HPLC)
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application(s):
__
storage temp.:
−20°C
SMILES string:
__
InChI:
__
InChI key:
__