5-Hydroxynicotinic acid
| Code | Size | Price |
|---|
| CDX-H0052-G001 | 1 g | £84.00 |
Quantity:
| CDX-H0052-G005 | 5 g | £132.00 |
Quantity:
| CDX-H0052-G025 | 25 g | £364.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+20°C
Documents
Further Information
Alternate Names/Synonyms:
5-Hydroxypyridine-3-carboxylic acid
Appearance:
White powder.
CAS:
27828-71-3
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C6H5NO3/c8-5-1-4(6(9)10)2-7-3-5/h1-3,8H,(H,9,10)
InChiKey:
ATTDCVLRGFEHEO-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 27828-71-3. Formula: C6H5NO3. MW: 139.11. Synthetic A nicotinic acid analog. Substrate analog MHPCO, used in the investigation of the hydroxylation mechanism of the flaovoprotein 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (MHPCO). Also used as building block for synthesis. Hydroxynicotinic acid is formed by the enzymatic action of nicotinate with nicotinic acid hydroxylase or nicotinate hydroxylase.
MDL:
MFCD00129117
Molecular Formula:
C6H5NO3
Molecular Weight:
139.11
Package Type:
Vial
Precautions:
P261, P264, P271, P280, P302, P352, P304, P340, P305, P351, P338, P312, P321, P332, P313, P337, P313, P362, P403, P233, P405, P501
Product Description:
A nicotinic acid analog. Substrate analog MHPCO, used in the investigation of the hydroxylation mechanism of the flaovoprotein 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (MHPCO). Also used as building block for synthesis. Hydroxynicotinic acid is formed by the enzymatic action of nicotinate with nicotinic acid hydroxylase or nicotinate hydroxylase.
Purity:
>97% (HPLC)
Signal word:
Warning
SMILES:
OC(=O)C1=CC(O)=CN=C1
Solubility Chemicals:
Soluble in DMSO.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +20°C.
References
(1) P. Chaiyen, et al.: Biochem. 43, 3933 (2004) | (2) P. Chaiyen, et al.: Biochemistry 36, 2612 (1997) | (3) P. Chaiyen, et al.: Biochemistry 36, 8060 (1997) | (4) P. Chaiyen, et al.: Biochemistry 36, 13856 (1997)
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