bicyclo[3.1.1]heptane-2-carboxaldehyde, 6,6-dimethyl-

CAS: 4764-14-1 C10 H16 O MW: 152.23672000

Identification

Namemyrtanal
IUPAC6,6-dimethylbicyclo[3.1.1]heptane-4-carbaldehyde
CAS Number4764-14-1
EINECS225-304-2
FDA UNIISearch
Molecular FormulaC10 H16 O
Molecular Weight152.23672000
Nikkaji NumberJ100.024A

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 200.67 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.320000 mmHg @ 25.00 °C. (est)
Flash Point 151.00 °F. TCC ( 65.90 °C. ) (est)
logP (o/w) 2.854 (est)
Soluble in water, 173 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

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

Safety in Use

Categorynatural substances and extractives
Recommendation for myrtanal usage levels up tonot for fragrance use.
Recommendation for myrtanal flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

philadelphus coronarius

Synonyms

bicyclo[3.1.1]heptane-2-carboxaldehyde, 6,6-dimethyl- 6,6- dimethyl bicyclo(3.1.1)heptane-2-carbaldehyde 6,6- dimethylbicyclo(3.1.1)heptane-2-carbaldehyde 6,6- dimethylbicyclo[3.1.1]heptane-2-carbaldehyde 6,6- dimethylbicyclo[3.1.1]heptane-4-carbaldehyde PubMed: Composition of essential oil from aerial and underground parts of Geum rivale and G. urbanum growing in Poland. PubMed: Essential oil compositions and antioxidant properties of the roots of twelve Anatolian Paeonia taxa with special reference to chromosome counts. PubMed: Lipophilic constituents from aerial and root parts of Mercurialis perennis L. PubMed: Anchoring effects in a wide binding pocket: the molecular basis of regioselectivity in engineered cytochrome P450 monooxygenase from B. megaterium. PubMed: Study of the carbonyl products of terpene/OH radical reactions: detection of the 2,4-DNPH derivatives by HPLC-MS.