Valproic acid
Also known as: 2-Propylpentanoic acid, Dipropylacetic acid, 2-Propylvaleric acid, 2-n-Propylpentanoic acid, 2-n-Propylvaleric acid, Di-n-propylacetic acid, Depakene, Depakine, Convulex, Ergenyl, Mylproin, Valproate
Valproic acid (CAS 99-66-1) is a compound in the Organic Acids category listed in the Jingsj chemical database. It has the molecular formula C8H16O2 and a molecular weight of 144.211 g/mol. Key properties include a melting point of 120 - 130ºC, a boiling point of 220.0±0.0 °C at 760 mmHg, a density of 0.9±0.1 g/cm3 and a flash point of 111.1±0.0 °C. It is classified under GHS with signal word Danger and hazard statements H302 — Harmful if swallowed, H315 — Causes skin irritation and H319 — Causes serious eye irritation. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.
- CAS No.
- 99-66-1
- Jingsj CID
- J-27785-0
- Molecular Formula
- C8H16O2
- Molecular Weight
- 144.211 g/mol
- Category
- Organic Acids
- Last updated
- 8/21/2026
No offers for this compound yet.
Request a quotePhysicochemical Properties
| Melting Point | 120 - 130ºC |
|---|---|
| Boiling Point | 220.0±0.0 °C at 760 mmHg |
| Density | 0.9±0.1 g/cm3 |
| Flash Point | 111.1±0.0 °C |
| Exact Mass | 144.115036 |
| PSA | 37.30000 |
| LogP | 2.72 |
| Vapor Pressure | 0.0±0.9 mmHg at 25°C |
| Refractive Index | 1.435 |
| Additional Property | slightly soluble |
GHS Safety & Compliance
- H302 — Harmful if swallowed
- H315 — Causes skin irritation
- H319 — Causes serious eye irritation
- H335 — May cause respiratory irritation
- H360 — May damage fertility or the unborn child
Activity & Biological Data
| Target | HDAC1:400 μM (IC50) HDAC:0.5-2 mM (IC50) HDAC2 Autophagy Mitophagy |
|---|---|
| Additional Information | [1]. Han BR, et al. Valproic acid inhibits the growth of HeLa cervical cancer cells via caspase-dependent apoptosis. Oncol Rep. 2013 Dec;30(6):2999-3005. [2]. Zhang ZH, et al. Valproic acid inhibits tumor angiogenesis in mice transplanted with Kasumi 1 leukemia cells. Mol Med Rep. 2013 Nov 28. [3]. Cohen OS, et al. Acute prenatal exposure to a moderate dose of valproic acid increases social behavior and alters gene expression in rats. Int J Dev Neurosci. 2013 Dec;31(8):740-50. [4]. Avery LB, et al. Valproic Acid Is a Novel Activator of AMP-Activated Protein Kinase and Decreases Liver Mass, Hepatic Fat Accumulation, and Serum Glucose in Obese Mice. Mol Pharmacol. 2014 Jan;85(1):1-10. [5]. Valproic acid, et al. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem. 2001 Sep 28;276(39):36734-41. |
Customs & Trade Information
| HS Code | 2915900090 |
|---|---|
| Summary | 2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0% |
Frequently Asked Questions
What is the CAS number of Valproic acid?
The CAS number of Valproic acid is 99-66-1.
What are the molecular formula and molecular weight of Valproic acid?
Valproic acid has molecular formula C8H16O2 and molecular weight 144.211 g/mol.
Is Valproic acid hazardous?
Valproic acid has GHS signal word Danger and hazard statements H302 — Harmful if swallowed; H315 — Causes skin irritation; H319 — Causes serious eye irritation.
What are the upstream and downstream products of Valproic acid?
For Valproic acid, Upstream Products: 2,2-Dipropylmalonic acid, 2-Propylvaleronitrile, Ethyl acetoacetate; Downstream Products: ethyl 2-bromo-2-propylpentanoate, 2-Propyl-1-pentanol, Sodium 2-propylpentanoate.
Data compiled from public chemical databases such as PubChem and supplier catalogs; supplier offers are provided by suppliers.
Last updated:
How to cite: Jingsj. "Valproic acid (CAS 99-66-1)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-27785-0 (accessed 2026-11-09).
Data for reference only; verify product details with suppliers before purchase.