Skip to main content

Sodium 2-propylpentanoate

Also known as: Sodium valproate, Valproate sodium, Valproic acid sodium salt, 2-Propylpentanoic acid sodium salt, 2-Propylvaleric acid sodium salt, Sodium dipropylacetate, Sodium 2-propylvalerate, Depacon, Epilim, Ergenyl, Depakine, MFCD00078604, UNII:5VOM6GYJ0D

Sodium 2-propylpentanoate (CAS 1069-66-5) is a compound in the Organic Acids category listed in the Jingsj chemical database. It has the molecular formula C8H15NaO2 and a molecular weight of 166.193 g/mol. Key properties include a melting point of 300 °C, a boiling point of 220ºC at 760 mmHg, a density of 1.0803 g/cm3 and a flash point of STABILITY. It is classified under GHS with signal word Warning and hazard statements H302 — Harmful if swallowed. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.
1069-66-5
Jingsj CID
J-19977-9
Molecular Formula
C8H15NaO2
Molecular Weight
166.193 g/mol
Category
Organic Acids
Last updated
8/21/2026

No offers for this compound yet.

Request a quote

Physicochemical Properties

Melting Point300 °C
Boiling Point220ºC at 760 mmHg
Density1.0803 g/cm3
Flash PointSTABILITY
Exact Mass166.096970
PSA40.13000
LogP0.95270
Vapor Pressure0.0435mmHg at 25°C
Additional Propertysoluble

GHS Safety & Compliance

IrritantSignal word: Warning
  • H302 — Harmful if swallowed

Activity & Biological Data

TargetHDAC1:400 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 Code2915900090
Summary2915900090 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 Sodium 2-propylpentanoate?

The CAS number of Sodium 2-propylpentanoate is 1069-66-5.

What are the molecular formula and molecular weight of Sodium 2-propylpentanoate?

Sodium 2-propylpentanoate has molecular formula C8H15NaO2 and molecular weight 166.193 g/mol.

Is Sodium 2-propylpentanoate hazardous?

Sodium 2-propylpentanoate has GHS signal word Warning and hazard statements H302 — Harmful if swallowed.

What are the upstream and downstream products of Sodium 2-propylpentanoate?

For Sodium 2-propylpentanoate, Upstream Products: Valproic acid; Downstream Products: Valproic acid.

Data compiled from public chemical databases such as PubChem and supplier catalogs; supplier offers are provided by suppliers.

Last updated:

How to cite: Jingsj. "Sodium 2-propylpentanoate (CAS 1069-66-5)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-19977-9 (accessed 2026-11-09).

Data for reference only; verify product details with suppliers before purchase.