Geranyllinalool - CAS 1113-21-9
Catalog: |
BB002752 |
Product Name: |
Geranyllinalool |
CAS: |
1113-21-9 |
Synonyms: |
(6E,10E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol |
IUPAC Name: | (6E,10E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol |
Description: | Geranyllinalool (CAS# 1113-21-9) is am aliphatic genaryl derivative. Geranyl Linalool unlike other genaryl derivatives showed poor inhibitory activity against carotenoid synthesis in Synechococcus. Geranyl Linalool was identified as a testosterone-dependent volatile compound in the preputial gland of rat Rattus norvegicus. |
Molecular Weight: | 290.48 |
Molecular Formula: | C20H34O |
Canonical SMILES: | CC(=CCCC(=CCCC(=CCCC(C)(C=C)O)C)C)C |
InChI: | InChI=1S/C20H34O/c1-7-20(6,21)16-10-15-19(5)14-9-13-18(4)12-8-11-17(2)3/h7,11,13,15,21H,1,8-10,12,14,16H2,2-6H3/b18-13+,19-15+ |
InChI Key: | IQDXAJNQKSIPGB-HQSZAHFGSA-N |
Boiling Point: | 250 °C |
Melting Point: | 51°C |
Flash Point: | 160°C |
Density: | 0.885 g/cm3 |
Solubility: | water, 0.006982 mg/L @ 25 °C (est) |
Appearance: | Clear colourless to pale yellowish liquid |
Storage: | Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00059363 |
LogP: | 6.12280 |
Refractive Index: | 1.486-1.492 |
Stability: | Stable under normal temperatures and pressures. |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113122393-A | Extraction, purification and detection method of acanthaceae volatile oil and application thereof | 20210521 |
CN-113200837-A | Novel synthesis process of K2-MK menatetrenone | 20210507 |
CN-111849632-A | Deep processing method of natural tobacco flavor raw material and application of natural tobacco flavor raw material in novel tobacco | 20200724 |
CN-111393275-A | Method for synthesizing intermediate farnesyl acetone and method for synthesizing phytol, isophytol and geranylgeraniol by using intermediate farnesyl acetone | 20200428 |
WO-2021153635-A1 | Highly safe non-lamellar liquid crystal forming composition | 20200127 |
PMID | Publication Date | Title | Journal |
22274813 | 20120301 | Terpene alcohols inhibit de novo sphingolipid biosynthesis | Planta medica |
22040000 | 20111201 | Isolation and identification of ligands for the goldfish testis androgen receptor in chemical recovery condensates from a Canadian bleached kraft pulp and paper mill | Environmental science & technology |
21334702 | 20110901 | The biochemistry of homoterpenes--common constituents of floral and herbivore-induced plant volatile bouquets | Phytochemistry |
20211182 | 20100515 | Identification of testosterone-dependent volatile compounds and proteins in the preputial gland of rat Rattus norvegicus | General and comparative endocrinology |
18640234 | 20081101 | Fragrance material review on geranyl linalool | Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association |
Complexity: | 394 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 2 |
Exact Mass: | 290.260965704 |
Formal Charge: | 0 |
Heavy Atom Count: | 21 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 290.260965704 |
Rotatable Bond Count: | 10 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 6.4 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Alkenes
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS