Latanoprost

Also known as: PHXA41, Xalatan, Xalata, 13,14-Dihydro-17-phenyl-18,19,20-trinor-PGF2a-isopropyl ester, Isopropyl (5Z)-7-{(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl}hept-5-enoate, 1-Methylethyl (5Z)-7-{(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl}hept-5-enoate

Latanoprost (CAS 130209-82-4) is a compound in the Organic Compounds category listed in the Jingsj chemical database. It has the molecular formula C26H40O5 and a molecular weight of 432.593 g/mol. Key properties include a boiling point of 583.8±50.0 °C at 760 mmHg, a density of 1.1±0.1 g/cm3 and a flash point of 188.3±23.6 °C. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.: 130209-82-4
Jingsj CID: J-1961099-2
Molecular Formula: C₂₆H₄₀O₅
Molecular Weight: 432.593 g/mol
Category: Organic Compounds
Last updated: 8/21/2026

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Physicochemical Properties

Boiling Point	583.8±50.0 °C at 760 mmHg
Density	1.1±0.1 g/cm3
Flash Point	188.3±23.6 °C
Exact Mass	432.287567
PSA	86.99000
LogP	3.65
Vapor Pressure	0.0±1.7 mmHg at 25°C
Refractive Index	1.538
Storage Conditions	−20°C
Additional Property	DMSO: freely soluble

Activity & Biological Data

Target	FP Receptor
Additional Information	[1]. Pauly A, et al. In vitro and in vivo comparative toxicological study of a new preservative-free latanoprost formulation. Invest Ophthalmol Vis Sci. 2012 Dec 13;53(13):8172-80. [2]. Tsai S, et al. The effect of topical latanoprost on anterior segment anatomic relationships in normal dogs. Vet Ophthalmol. 2013 Sep;16(5):370-6. [3]. Zheng J, et al. Latanoprost promotes neurite outgrowth in differentiated RGC-5 cells via the PI3K-Akt-mTOR signaling pathway. Cell Mol Neurobiol. 2011 May;31(4):597-604. [4]. Ooi YH, et al. Effect of bimatoprost, latanoprost, and unoprostone on matrix metalloproteinases and their inhibitors in human ciliary body smooth muscle cells. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5259-65. [5]. B'Ann True Gabelt, et al. Prostaglandin Subtype-Selective and Non-Selective IOP-Lowering Comparison in Monkeys.

Target

FP Receptor

Additional Information

[1]. Pauly A, et al. In vitro and in vivo comparative toxicological study of a new preservative-free latanoprost formulation. Invest Ophthalmol Vis Sci. 2012 Dec 13;53(13):8172-80. [2]. Tsai S, et al. The effect of topical latanoprost on anterior segment anatomic relationships in normal dogs. Vet Ophthalmol. 2013 Sep;16(5):370-6. [3]. Zheng J, et al. Latanoprost promotes neurite outgrowth in differentiated RGC-5 cells via the PI3K-Akt-mTOR signaling pathway. Cell Mol Neurobiol. 2011 May;31(4):597-604. [4]. Ooi YH, et al. Effect of bimatoprost, latanoprost, and unoprostone on matrix metalloproteinases and their inhibitors in human ciliary body smooth muscle cells. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5259-65. [5]. B'Ann True Gabelt, et al. Prostaglandin Subtype-Selective and Non-Selective IOP-Lowering Comparison in Monkeys.

Customs & Trade Information

HS Code	2937500000

Frequently Asked Questions

What is the CAS number of Latanoprost?

The CAS number of Latanoprost is 130209-82-4.

What are the molecular formula and molecular weight of Latanoprost?

Latanoprost has molecular formula C26H40O5 and molecular weight 432.593 g/mol.

What are the upstream and downstream products of Latanoprost?

For Latanoprost, Upstream Products: 2-Iodopropane, Latanoprost acid, Isopropanol; Downstream Products: Latanoprost acid.

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

Last updated: 8/21/2026

How to cite: Jingsj. "Latanoprost (CAS 130209-82-4)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-1961099-2 (accessed 2026-11-09).

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