Identification

Namenopol
IUPAC2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol
CAS Number128-50-7
EINECS204-890-3
FDA UNIIXK8HU7WJQC
Molecular FormulaC11 H18 O
Molecular Weight166.26366000
Nikkaji NumberJ21.520A

Regulatory

JECFA Food Flavoring986 10-hydroxymethylene-2-pinene
DG SANTE Food Flavourings02.141 2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethan-1-ol
FEMA Number3938
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)128-50-7 ; 10-HYDROXYMETHYLENE-2-PINENE

Physical Properties

Appearance colorless clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.96500 to 0.97300 @ 25.00 °C.
Pounds per Gallon - (est). 8.030 to 8.096
Refractive Index 1.49000 to 1.50000 @ 20.00 °C.
Boiling Point 110.50 °C. @ 10.00 mm Hg, 230.00 °C. @ 760.00 mm Hg
Vapor Pressure 0.009000 mmHg @ 25.00 °C. (est)
Flash Point 210.00 °F. TCC ( 98.89 °C. )
logP (o/w) 3.152 (est)
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Strength medium
Substantivity 32 hour(s) at 100.00 %
Odor Description
at 100.00 %.
Very mild, woody-camphoraceous
characteristic, soft woody (pine note)
Odor sample from Ungerer & Company, Inc.

Safety Information

European informationMost important hazard(s):
Oral/Parenteral Toxicityoral-rat LD50 890 mg/kg
Dermal Toxicityskin-rabbit LD50 > 5000 mg/kg
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for nopol usage levels up to8.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)33.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA)0.01 (μg/capita/day)
Threshold of Concern1800 (μg/person/day)
Structure ClassI
baked goods2.00000
beverages(nonalcoholic)-
beverages(alcoholic)-
breakfast cereal-
cheese-
chewing gum2.00000
condiments / relishes-
confectionery froastings-
egg products-
fats / oils-
fish products-
frozen dairy1.00000
fruit ices-
gelatins / puddings2.00000
granulated sugar-
gravies-
hard candy4.00000
imitation dairy-
instant coffee / tea-
jams / jellies-
meat products-
milk products-
nut products-
other grains-
poultry-
processed fruits-
processed vegetables-
reconstituted vegetables-
seasonings / flavors-
snack foods-
soft candy1.50000
soups-
sugar substitutes-
sweet sauces-

Berje Inc.

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SRS Aromatics Ltd

For over 25 years

Bringing flavour and fragrance into your world.

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Vigon International

Passion for Simplicity

Manufacturer and supplier of high quality flavor and fragrance ingredients.

View All Website 570-476-6300 sales@vigon.com

Potential Uses

FR alpine bouquet FR balsam FR citrus fir FR green grass FR herbal FR pine FR woody

Natural Occurrence

carrot root orange bigarade oil @ 0.36% Data rosemary plant

Synonyms

bicyclo(3.1.1)hept-2-ene-2-ethanol, 6,6-dimethyl- bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-dimethyl- 2-(6,6- dimethyl bicyclo(3.1.1)hept-2-en-2-yl) ethan-1-ol 6,6- dimethyl-2-hydroxyethyl-6,6-dimethyl bicyclo(3,1,1)hept-2-ene bicyclo(3.1.1)hept-2-ene-2-ethanol 6,6- dimethyl-2-norpinene-2-ethanol 6,6- dimethylbicyclo-(3.1.1)-2-heptene-2-ethanol 2-(6,6- dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethan-1-ol 2-(6,6- dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol 6,6- dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol 2- hydroxyethyl-6,6-dimethyl-bicyclo[3,1,1]-hept-2-ene 10- hydroxymethylene-2-pinene homo myrtenol 2-nor pinene-2-ethanol, 6,6-dimethyl- PubMed: Superior performance of metal-organic frameworks over zeolites as solid acid catalysts in the Prins reaction: green synthesis of nopol. PubMed: On the synergistic catalytic properties of bimetallic mesoporous materials containing aluminum and zirconium: the Prins cyclisation of citronellal. PubMed: Microbial transformation of (-)-nopol benzyl ether: direct dihydroxylation of benzene ring. PubMed: Transition metal-substituted Dawson anions as chemo- and regio-selective oxygen transfer catalysts for H2O2 in the epoxidation of allylic alcohols. PubMed: Antioxidant responses and reactive oxygen species generation in different body regions of the estuarine polychaeta Laeonereis acuta (Nereididae). PubMed: Analysis of the essential oil composition of eight Anthemis species from Greece. PubMed: Mesoporous iron phosphate as an active, selective and recyclable catalyst for the synthesis of nopol by Prins condensation. PubMed: Synthesis of nopol over MCM-41 catalysts. PubMed: Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols. PubMed: Enzymatic synthesis of structural analogs of PAF-acether by phospholipase D-catalysed transphosphatidylation. PubMed: Glucuronidation of 2-arylpropionic acids pirprofen, flurbiprofen, and ibuprofen by liver microsomes. PubMed: Differential action of thyroid hormones and chemically related compounds on the activity of UDP-glucuronosyltransferases and cytochrome P-450 isozymes in rat liver. PubMed: Effect of 1-benzylimidazole on cytochromes P-450 induction and on the activities of epoxide hydrolases and UDP-glucuronosyltransferases in rat liver. PubMed: Properties of human hepatic UDP-glucuronosyltransferases. Relationship to other inducible enzymes in patients with cholestasis. PubMed: [On a new local anesthetic. Homomyrtenol and diethylaminoethanol ether].