Camphor
AKA “D-CAMPHOR, (R)-(+)-Camphor, (1R, (R)-Camphor, (1R)-(+)-Camphor, Alcanfor, Japanese camphor, d-2-Camphanone
Synthetic
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Ingredient Facts
Camphor
AKA: D-CAMPHOR, (R)-(+)-Camphor, (1R, (R)-Camphor, (1R)-(+)-Camphor, Alcanfor, Japanese camphor, D-2-Camphanone
Synthetic · Denaturant | Plasticiser | Soothing | Antimicrobial | Astringent · EWG: 4
Plant-Derived
Preservative
Soothing
Astringent
Synthetic
Clean
Camphor provides a cooling, refreshing sensation and helps improve product texture and performance.
Solubility less than 1 mg/mL at 59 °F (NTP, 1992)
Formula
C10H16O
Mol. Weight
152.23
CAS #
464-49-3, 76-22-2
Form
Wax
Plant-Derived
Synthetic. Derived from pinene, a volatile hydrocarbon found in pine oil and turpentine, through oxidative cyclization processes. Synthesized via catalytic oxidation of alpha-pinene or through hydrogenation of camphorquinone to produce the crystalline ketone compound.
Function
Denaturant | Plasticiser | Soothing | Antimicrobial | Astringent
Traditional Use
Used in Ayurvedic and Traditional Chinese Medicine for over 2,000 years as a cooling and stimulating agent for skin. Historically valued in topical preparations for its analgesic and antimicrobial properties, derived from camphor laurel trees.
Skin Types
all-skin-types
Best For
Target
Irritation
Melanin-Rich Skin
Suitable
Pregnancy Safe
Caution
EWG Score4
CIR Safety Findings
ewg-4, all-shades-safe
Concentration Guide
3%
0%4%
Reg. Limit
FDA OTC limit: 3% (Anorectal Analgesic). Anorectal use only. External analgesic counterirritant monograph (21 CFR 348) was never finalized for topical pain relief. Source: FDA OTC Monograph, 21 CFR 346.16
Regulatory Status
USApermitted
EUrestricted
JAPANrestricted
CANADArestricted
Verified Feb 2026
Data: PubChem · CosIng · EWG · CIR