Quinolinic acid
Also known as Pyridine-2,3-dicarboxylic acid, 2,3-pyridinedicarboxylic acid, quinolinate
Key facts
What buyers check first
- Appearance
- Crystals
- Melting point
- 228.5 ยฐC
- Solubility
- Soluble in 180 parts water, in alkalies, slightly in alcohol. Almost insol in ether or bโฆ
- HS code
- 293339
- Category
- Herbicides

What is Quinolinic acid?
Plain description, key identifiers and synonyms
Quinolinic acid is a pyridinedicarboxylic acid that is pyridine substituted by carboxy groups at positions 2 and 3. It is a metabolite of tryptophan. It has a role as a NMDA receptor agonist, a mouse metabolite, an Escherichia coli metabolite and a human metabolite. It is a conjugate acid of a quinolinate and a quinolinate(1-).
Identifiers
Registry numbers, names and line notations, tap to copy
- IUPAC name
- pyridine-2,3-dicarboxylic acid
- CAS number
- 89-00-9 CAS number cross-checkedOther or deprecated CAS: 28605-84-7, 339155-13-4
- EC number
- 201-874-8
- Molecular formula
- C7H5NO4
- UNII
- F6F0HK1URN
- MDL number
- MFCD00006295
- InChIKey
- GJAWHXHKYYXBSV-UHFFFAOYSA-N
- InChI
- InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-8-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12)
- SMILES (canonical and isomeric)
- C1=CC(=C(N=C1)C(=O)O)C(=O)O
Synonyms
- Pyridine-2,3-dicarboxylic acid
- 2,3-pyridinedicarboxylic acid
- quinolinate
- Pyridine-2,3-dicarboxylate
- Pyridin-2,3-dicarbonsaeure
- 2,3-pyridine dicarboxylic acid
- pyridinedicarboxylic acid
- Tocris-0225
- pyridine-2,3-carboxylate
- 2,3-pyridinedicarboxylate
- quinolinic-acid
- pyridine carboxylate, 6c
- pyridine, 2,3-dicarboxy-
- Quinolinic acid (Standard)
- DivK1c_000773
- Pyridine-2,3-dicarboxylicacid
- pyridine-5,6-dicarboxylic acid
- Moxifloxacin Impurity cent feminine
- PDSP1_000133
- PDSP2_000132
- 2,3-Pyridinedicarboxylic acid, 99%
- Sdccgmls-0411909.p028
- Sdccgsbi-0050962.p003
- 2,3-Pyridinedicarboxylic acid (8CI,9CI)
- Quinolinic acid Solution in Methanol, 100ug/mL
Show all 27 synonymsShow fewer synonyms
- Quinolinic acid Solution in Methanol, 1000ug/mL
- 2,3-Pyridinedicarboxylic acid, Vetec(TM) reagent grade, 98%
Physical and chemical properties
Measured values and descriptors computed from the structure
Physical and chemical properties
Measured values, check the supplier specification for your grade
| Appearance | Crystalsexp.Measured value |
|---|---|
| Odour | Odorlessexp.Measured value |
| Melting point | 228.5 ยฐCexp.Measured value |
| Solubility | Soluble in 180 parts water, in alkalies, slightly in alcohol. Almost insol in ether or benzene.exp.Measured value |
Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.
Computed descriptors
Calculated from the structure, useful for screening and formulation
| Molecular weight | 167.12 g/molcalc.Computed value |
|---|---|
| Exact mass | 167.0219 Dacalc.Computed value |
| LogP (octanol/water) | 0.48calc.Computed value |
| Topological polar surface area | 87.49 ร
ยฒcalc.Computed value |
| Hydrogen bond donors | 2calc.Computed value |
| Hydrogen bond acceptors | 3calc.Computed value |
| Rotatable bonds | 2calc.Computed value |
| Heavy atoms | 12calc.Computed value |
| Rings | 1calc.Computed value |
| Aromatic rings | 1calc.Computed value |
| Fraction sp3 carbons | 0calc.Computed value |
| Formal charge | 0calc.Computed value |
| Stereocentres | 0calc.Computed value |
| Lipinski rule of five | Passes (0 violations)calc.Computed value |
Calculated for screening. Confirm critical figures with the supplier.
Murcko scaffold
The ring system that remains when every side chain is removed
Safety and hazards
GHS classification summary, not a safety data sheet
Hazard statements
- H302Harmful if swallowed.
- H315Causes skin irritation.
- H318Causes serious eye damage.
- H319Causes serious eye irritation.
- H335May cause respiratory irritation.
Precautionary statements (21)
- P261Avoid breathing dust, fume, gas, mist, vapours or spray.
- P264Wash skin thoroughly after handling.
- P264 + P265Wash skin thoroughly after handling. Do not touch eyes.
- P270Do not eat, drink or smoke when using this product.
- P271Use only outdoors or in a well-ventilated area.
- P280Wear protective gloves, protective clothing, eye protection and face protection.
- P301 + P317If swallowed: Get medical help.
- P302 + P352If on skin: Wash with plenty of water.
- P304 + P340If inhaled: Remove person to fresh air and keep comfortable for breathing.
- P305 + P351 + P338If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
- P305 + P354 + P338If in eyes: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
- P317Get medical help.
- P319Get medical help if you feel unwell.
- P321Specific treatment (see supplemental first aid instructions on the label).
- P330Rinse mouth.
- P332 + P317If skin irritation occurs: Get medical help.
- P337 + P317If eye irritation persists: Get medical help.
- P362 + P364Take off contaminated clothing. And wash it before reuse.
- P403 + P233Store in a well-ventilated place. Keep container tightly closed.
- P405Store locked up.
- P501Dispose of contents and container in accordance with local regulations.
GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.
Full safety data and first aidQuinolinic acid suppliers
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Where suppliers are based
123 suppliers in 15 countries
- China50
- United States39
- Germany6
- United Kingdom6
- Canada3
- India3
- and 9 more countries
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Quinolinic acid price
Indicative price range per kg from live supplier offers
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Uses and applications
What the substance is used for, by industry and function
Quinolinic acid (QUIN), a pyridine dicarboxylic acid and metabolite of tryptophan, which has been detected in the central nervous system (CNS), behaves as an excitotoxin /and is being used as a research tool to examine the role of excitotoxicity in neuronal degeneration associated with a number of neurological diseases (Alzheimer's disease, Huntington's disease, Parkinson's disease) which involve selective neurotransmitter deficits./.
Quinolinic acid levels in CSF (a surrogate marker of neuronal cell damage) / are used to evaluate HIV disease progression in research settings./.
Used to manufacture the herbicide Assert (imazapyr) ... and as an intermediate in the production of nicotinic acid.
Industrial uses: Intermediate.
Consumer uses: Intermediate.
Use classes: Cosmetics.
Roles
- Escherichia coli metabolite
- NMDA receptor agonist
- animal metabolite
- bacterial metabolite
- eukaryotic metabolite
- excitatory amino acid agonist
- human metabolite
- mammalian metabolite
- metabolite
- mouse metabolite
- neurotransmitter agent
- pharmaceutical
- prokaryotic metabolite
Pharmacology
Quinolinic Acid is an intermediate product of the kynurenine pathway, which is responsible for the conversion of the amino acid tryptophan into nicotinamide adenine dinucleotide, with potential neurotoxic activity. If produced in excess, quinolinic acid can cross the blood-brain barrier (BBB) and function as an N-methyl-D-aspartate (NMDA) receptor agonist, which may lead to both neuronal damage and neurodegenerative brain disease. The NMDA receptor, a heterotetrameric, ligand-gated and voltage-dependent glutamate receptor, is critical for synaptic plasticity, learning and memory.
How it is made
Preparation: S. Hoogewerff, W. A. van Dorp, Ber. 12, 747 (1879), W. Koenigs, ibid. 983, O. fischer, E. Renouf, ibid. 17, 755 (1884), E. Sucharda, ibid. 58B, 1727(1925), v. Yu. Stiks, S. A. Bulgach, ibid. 65B, 11 (1932), A.F. Lindenstruth, C.A. VanderWerf, J. Am. Chem. Soc. 71, 3020 (1949).
Regulatory status
Inventories, regulations and trade controls that list this substance
United States
- TSCA inventory (USA)Status: Active in US commerce
HS code and trade data
Customs classification and reported world trade statistics
Global trade
World import and export statistics for the HS code Quinolinic acid is traded under.
Heterocyclic compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structureโฆ
- Germany14.2%
- United States12.8%
- Brazil10.1%
* Partner reported figures, a lower bound.
The HS code shown for Quinolinic acid is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.
Frequently asked questions
Quick answers about Quinolinic acid, based on the data on this page
What is Quinolinic acid?
What is the CAS number of Quinolinic acid?
What is the molecular formula and weight of Quinolinic acid?
What is Quinolinic acid used for?
Is Quinolinic acid hazardous?
What is the HS code of Quinolinic acid?
Where can I buy Quinolinic acid?
Where can I buy Quinolinic acid in India?
What is the price of Quinolinic acid?
Guides for buyers
Practical guides that help when you source, ship or handle Quinolinic acid
- Guide, SafetyHow to read a safety data sheet in 10 minutesA section by section method to pull the essentials out of any 16 section SDS: identity, hazards, composition, storage, PPE, properties, transport and emergency measures.Read
- Guide, SafetyGHS pictograms, signal words and hazard statements explainedA practical guide to the nine GHS pictograms, the signal words Danger and Warning, H and P statements, and how to read a chemical label in seconds.Read
- Article, SourcingHow to write an RFQ that gets fast and accurate quotesWhat suppliers need to quote quickly and comparably: exact product identity, quantity and packing, delivery terms, documents, samples and payment, with a ready to use template.Read
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