(±)-Camphor

Also known as: Camphor, DL-Camphor, 2-Bornanone, 2-Camphanone, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one, (±)-Camphor, (+/-)-Camphor, Camphor synthetic, Racemic camphor

(±)-Camphor (CAS 76-22-2) is a compound in the Organic Compounds category listed in the Jingsj chemical database. It has the molecular formula C10H16O and a molecular weight of 152.233 g/mol. Key properties include a melting point of 175-177 °C(lit.), a boiling point of 207.4±0.0 °C at 760 mmHg, a density of 1.0±0.1 g/cm3 and a flash point of 64.4±0.0 °C. It is classified under GHS with signal word Warning and hazard statements H228, H302 — Harmful if swallowed and H332 — Harmful if inhaled. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.: 76-22-2
Jingsj CID: J-35931-9
Molecular Formula: C₁₀H₁₆O
Molecular Weight: 152.233 g/mol
Category: Organic Compounds
Last updated: 8/21/2026

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Physicochemical Properties

Melting Point	175-177 °C(lit.)
Boiling Point	207.4±0.0 °C at 760 mmHg
Density	1.0±0.1 g/cm3
Flash Point	64.4±0.0 °C
Exact Mass	152.120117
PSA	17.07000
LogP	2.13
Additional Property	5.2 (vs air)
Vapor Pressure	0.2±0.4 mmHg at 25°C
Refractive Index	1.485
Additional Property	0.12 g/100 mL (25 ºC)

GHS Safety & Compliance

Flammable / Irritant / Health HazardSignal word: Warning

H228
H302 — Harmful if swallowed
H332 — Harmful if inhaled
H371 — May cause damage to organs

Activity & Biological Data

Target	TRPV3[2]
Additional Information	[1]. Chen W, et al. Camphor--a fumigant during the Black Death and a coveted fragrant wood in ancient Egypt and Babylon--a review. Molecules. 2013 May 10;18(5):5434-54. [2]. Billen B, et al. Different ligands of the TRPV3 cation channel cause distinct conformational changes as revealedby intrinsic tryptophan fluorescence quenching. J Biol Chem. 2015 May 15;290(20):12964-74. [3]. Tran TA, et al. Camphor Induces Proliferative and Anti-senescence Activities in Human Primary Dermal Fibroblasts and Inhibits UV-Induced Wrinkle Formation in Mouse Skin. Phytother Res. 2015 Dec;29(12):1917-25.

Target

TRPV3[2]

Additional Information

[1]. Chen W, et al. Camphor--a fumigant during the Black Death and a coveted fragrant wood in ancient Egypt and Babylon--a review. Molecules. 2013 May 10;18(5):5434-54. [2]. Billen B, et al. Different ligands of the TRPV3 cation channel cause distinct conformational changes as revealedby intrinsic tryptophan fluorescence quenching. J Biol Chem. 2015 May 15;290(20):12964-74. [3]. Tran TA, et al. Camphor Induces Proliferative and Anti-senescence Activities in Human Primary Dermal Fibroblasts and Inhibits UV-Induced Wrinkle Formation in Mouse Skin. Phytother Res. 2015 Dec;29(12):1917-25.

Customs & Trade Information

HS Code	2914291000

Frequently Asked Questions

What is the CAS number of (±)-Camphor?

The CAS number of (±)-Camphor is 76-22-2.

What are the molecular formula and molecular weight of (±)-Camphor?

(±)-Camphor has molecular formula C10H16O and molecular weight 152.233 g/mol.

Is (±)-Camphor hazardous?

(±)-Camphor has GHS signal word Warning and hazard statements H228; H302 — Harmful if swallowed; H332 — Harmful if inhaled.

What are the upstream and downstream products of (±)-Camphor?

For (±)-Camphor, Upstream Products: DL-2-Bornanol, DL-Isoborneol, D-3-Bromocamphor; Downstream Products: (R)-(+)-Bornylamine, 1,2,3,5-tetramethylbenzene, Campholenic aldehyde.

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. "(±)-Camphor (CAS 76-22-2)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-35931-9 (accessed 2026-11-09).

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