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phenethyl pivalate

Phenethyl pivalate is a medium-strength floral ester with balsamic notes, used as a fragrance and flavor agent in perfumery and related applications.
Chemical Structure

General Material Description

Phenethyl pivalate, also known as 2-phenylethyl pivalate or centifolyl, is a synthetic ester with the molecular formula C13H18O2. It appears as a clear, colorless liquid predominantly used in flavor and fragrance industries. This compound emits a medium-strength floral odor with balsamic, rose, and spicy nuances, contributing to its popularity in perfuming agents. Phenethyl pivalate is referenced under controlled vocabularies such as ChEBI (CHEBI:87336). Typically derived via esterification of 2-phenylethanol and pivalic acid, it is valued for its ability to impart floral and fruity notes in formulations.

Occurrence, Applicability & Potential Uses

Phenethyl pivalate is primarily a synthetic aromatic ester and does not occur naturally in significant amounts. It is extensively used as a flavor and fragrance ingredient that evokes floral, fruity, and balsamic characteristics. Its odor profile includes hints reminiscent of rose, geranium, jasmine, lilac, and blueberry, which makes it suitable for use in perfumes, soaps, antiperspirants, and other personal care products. The compound is featured in formulary standards such as FEMA (US), which guides its use within safe concentration limits, typically allowing up to 8% usage in fragrance concentrates. This regulatory framework ensures phenethyl pivalate’s compatibility and safety in cosmetic and personal hygiene products.

Physico-Chemical Properties Summary

Phenethyl pivalate exhibits a moderate molecular weight of 206.28 g/mol and presents as a clear liquid with a refractive index ranging between 1.48 and 1.482 at 20 °C. Its specific gravity is approximately 0.968 to 0.975 at 25 °C, indicating it is slightly less dense than water. The compound has an estimated logP of 3.572, suggesting moderate lipophilicity which influences its solubility and bio-distribution in formulations. Phenethyl pivalate has a low vapor pressure of about 0.005 mmHg at 25 °C, contributing to its substantivity and longevity in fragrances. Its flash point is around 93 °C (200 °F), indicating moderate volatility and flammability considerations. Solubility is favorable in alcohols but limited in water, which affects mixing and application in various product bases.

FAQ

What is phenethyl pivalate and what are its key fragrance properties?
Phenethyl pivalate is a synthetic ester used primarily as a fragrance and flavor agent. It emits a medium-strength floral aroma with balsamic, rose, spice, and fruity undertones. This compound contributes to scents reminiscent of geranium, jasmine, lilac, and blueberry. Its notable substantivity means it can last up to 40 hours at full concentration, making it valuable for long-lasting fragrance formulations.
Where is phenethyl pivalate commonly used and how is it applied in products?
Phenethyl pivalate is widely used in perfumery, personal care, and flavor industries. It enhances floral and fruity scents in perfumes, soaps, antiperspirants, and household cleansers. Its compatibility with alcohol solvents and limited water solubility supports its use in various formulation bases. Regulatory standards from FEMA (US) typically permit its use up to 8% in fragrance concentrates, allowing safe incorporation for enhancing aromatic profiles.
What safety regulations govern the use of phenethyl pivalate and how is it sourced?
Phenethyl pivalate is governed by international safety assessments, including the IFRA (Global) Code of Practice and FEMA (US) guidelines, which outline maximum concentration limits for consumer safety. It is classified as an irritant under European classifications, requiring precautions to avoid skin and eye contact during handling. The compound is synthesized industrially through esterification processes and obtained commercially for use in flavor and fragrance applications.

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2915.60.9000
ChemSpider:View

General Material Information

Preferred name phenethyl pivalate
Trivial Name 2-Phenylethyl pivalate
Short Description centifolyl
Formula C13 H18 O2
CAS Number 67662-96-8
ECHA Number 266-841-2
FDA UNII Search
Nikkaji Number J333.265I
NMR Predictor External link
Synonyms
  • centifloyl
  • centifolyl
  • centirose (Tadimety)
  • 2,3-dimethyl propanoic acid 2-phenethyl ester
  • 2,2-dimethyl propanoic acid 2-phenyl ethyl ester
  • phenethyl trimethyl acetate
  • 2-phenyl ethyl 2,2-dimethyl propanoate
  • phenyl ethyl pivalate
  • phenyl ethyl pivilate
  • phenyl ethyl trimethyl acetate
  • 2-phenylethyl 2,2-dimethylpropanoate
  • 2-phenylethyl pivalate
  • phenylethyl-pivalate
  • pivarose
  • propanoic acid, 2,2-dimethyl-, 2-phenylethyl ester
  • 2-phenylethyl 2,2-dimethylpropanoate
  • 2-Phenylethyl pivalate

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 206.28486633301
Specific gravity @ 25 °C
Pounds per Gallon 8.055 to 8.113
Refractive Index 1.48 to 1.482 @ 20 °C
Vapor Pressure 0.005 mmHg @ 25 °C
Flash Point TCC Value 93.33 °C TCC
logP (o/w) 3.572 est
Solubility
alcohol Yes
water, 17.74 mg/L @ 25 °C (est) Yes
water No

Organoleptic Properties

Odor Type: Floral
rose, spicy, rose red rose, geranium, blueberry
Odor strength medium
Substantivity 40 hour(s) at 100.00 %
Luebke, William tgsc, (1985) At 100.00 %. rose spice rhodinol geranium blueberry
Flavor Type: Balsamic
balsamic, rose tea rose, spicy, geranium, green, grassy, powdery, waxy
Luebke, William tgsc, (1985) Balsamic tea rose spicy geranium green grassy waxy

Potential Uses

Applications
Odor purposes Blueberry , Carnation , Floral , Geranium , Hyacinth , Jasmin , Lilac , Rose , Rose red rose , Spice
Other purposes Antiperspirants , Clean
Cosmetic purposes Perfuming agents

Safety Information

Safety information

European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for phenethyl pivalate usage levels up to:
8.0000 % in the fragrance concentrate.

Safety references

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):67662-96-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :105516
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2-phenylethyl 2,2-dimethylpropanoate
Chemidplus:0067662968