(+)-Citronellal structure
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Common Name | (+)-Citronellal | ||
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CAS Number | 2385-77-5 | Molecular Weight | 154.25 | |
Density | 0.8±0.1 g/cm3 | Boiling Point | 208.4±9.0 °C at 760 mmHg | |
Molecular Formula | C10H18O | Melting Point | 25°C | |
MSDS | Chinese USA | Flash Point | 75.6±0.0 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of (+)-Citronellal(R)-(+)-Citronellal, isolated from citrus, lavender and eucalyptus oils, is a monoterpenoid and main component of citronellal oil with a distinct lemon scent. A flavouring agent. Used for insect repellent and antifungal properties[1][2]. |
Name | (R)-(+)-citronellal |
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Synonym | More Synonyms |
Description | (R)-(+)-Citronellal, isolated from citrus, lavender and eucalyptus oils, is a monoterpenoid and main component of citronellal oil with a distinct lemon scent. A flavouring agent. Used for insect repellent and antifungal properties[1][2]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
References |
Density | 0.8±0.1 g/cm3 |
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Boiling Point | 208.4±9.0 °C at 760 mmHg |
Melting Point | 25°C |
Molecular Formula | C10H18O |
Molecular Weight | 154.25 |
Flash Point | 75.6±0.0 °C |
Exact Mass | 154.135757 |
PSA | 17.07000 |
LogP | 3.48 |
Vapour Pressure | 0.2±0.4 mmHg at 25°C |
Index of Refraction | 1.437 |
Storage condition | 2-8°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2912190090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2912190090 |
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Summary | 2912190090 acyclic aldehydes without other oxygen function。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0% |
'Dopamine-first' mechanism enables the rational engineering of the norcoclaurine synthase aldehyde activity profile.
FEBS J. 282(6) , 1137-51, (2015) Norcoclaurine synthase (NCS) (EC 4.2.1.78) catalyzes the Pictet-Spengler condensation of dopamine and an aldehyde, forming a substituted (S)-tetrahydroisoquinoline, a pharmaceutically important moiety... |
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Monoterpene (-)-citronellal affects hepatocarcinoma cell signaling via an olfactory receptor.
Arch. Biochem. Biophys. 566 , 100-9, (2015) Terpenes are the major constituents of essential oils in plants. In recent years, terpenes have become of clinical relevance due to their ability to suppress cancer development. Their effect on cellul... |
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Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): Identification of phenmedipham and amperozide as FAAH inhibitors
Bioorg. Med. Chem. Lett. 19 , 6793-6, (2009) The screening of known medicinal agents against new biological targets has been shown to be a valuable approach for revealing new pharmacology of marketed compounds. Recently, carbamate, urea and keto... |
Citronellal |
d-Diltiazem |
(R)-3,7-Dimethyl-6-octenal |
EINECS 219-194-5 |
MFCD00067089 |
(3R)-3,7-Dimethyloct-6-enal |
6-Octenal, 3,7-dimethyl-, (3R)- |
DILTIAZEN |
(+)-Citronellal |
(3R)-(+)-citronellal |
d-cis-diltiazem |
Adizem XL |
6-Octenal, 3,7-dimethyl-, (R)- |
D-Citronellal |
(R)-3,7-dimethyloct-6-enal |
TILDIEM300LP |
(3R)-3,7-Dimethyl-6-octenal |
Coras |
(R)-(+)-3,7-Dimethyl-6-octenal |