Cyclopentadecanone
- Product Name
- Cyclopentadecanone
- CAS No.
- 502-72-7
- Chemical Name
- Cyclopentadecanone
- Synonyms
- MUSK 15;exalton;EXALTONE;Normuscon;NORMUSCONE;CYCLOPENTADECONE;Cyclopentadecanon;CYCLOPENTADECANONE;CYCLOPENTANDECANONE;Exaltone~Normuscone
- CBNumber
- CB2416348
- Molecular Formula
- C15H28O
- Formula Weight
- 224.38
- MOL File
- 502-72-7.mol
Cyclopentadecanone Property
- Melting point:
- 63-65 °C (lit.)
- Boiling point:
- 120 °C/0.3 mmHg (lit.)
- Density
- 0.897 g/mL at 25 °C (lit.)
- vapor pressure
- 0.009Pa at 40℃
- refractive index
- 1.4637 (estimate)
- Flash point:
- 120°C/0.3mm
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Alcohol
- form
- powder to crystal
- color
- Colourless crystal needles.
- Odor
- at 10.00 % in dipropylene glycol. powdery musk animal natural greasy
- Odor Type
- musk
- Water Solubility
- 578μg/L at 20℃
- BRN
- 1618444
- LogP
- 5.6 at 20℃
- CAS DataBase Reference
- 502-72-7(CAS DataBase Reference)
- NIST Chemistry Reference
- Cyclopentadecanone(502-72-7)
- EPA Substance Registry System
- Cyclopentadecanone (502-72-7)
Safety
- Safety Statements
- 22-24/25
- WGK Germany
- 2
- RTECS
- GY0900000
- TSCA
- Yes
- HS Code
- 29142900
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P233Keep container tightly closed.
P260Do not breathe dust/fume/gas/mist/vapours/spray.
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P304IF INHALED:
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P321Specific treatment (see … on this label).
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P337+P313IF eye irritation persists: Get medical advice/attention.
P340Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P362Take off contaminated clothing and wash before reuse.
P403Store in a well-ventilated place.
P403+P233Store in a well-ventilated place. Keep container tightly closed.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- C111201
- Product name
- Cyclopentadecanone
- Purity
- 98%
- Packaging
- 5g
- Price
- $82.2
- Updated
- 2024/03/01
- Product number
- C1422
- Product name
- Cyclopentadecanone
- Purity
- >98.0%(GC)
- Packaging
- 5g
- Price
- $43
- Updated
- 2024/03/01
- Product number
- C1422
- Product name
- Cyclopentadecanone
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $171
- Updated
- 2024/03/01
- Product number
- A17652
- Product name
- Cyclopentadecanone, 99%
- Packaging
- 5g
- Price
- $54.5
- Updated
- 2021/12/16
- Product number
- A17652
- Product name
- Cyclopentadecanone, 99%
- Packaging
- 1g
- Price
- $13.1
- Updated
- 2021/12/16
Cyclopentadecanone Chemical Properties,Usage,Production
Chemical Properties
WHITE CRYSTALLINE POWDER
Chemical Properties
Cyclopentadecanone is a musk fragrance found in the
scent gland of the male civet cat.
A number of syntheses have been developed for its manufacture [260]. Among
these, the so-called Story procedure is the only route that has the potential to
make cyclopentadecanone available on a larger scale, but due to the handling of
hydroperoxides, the process is difficult to manage.
The process starts from tricyclohexylidene triperoxide, which is obtained by
oxidation of cyclohexanone with hydrogen peroxide. Pyrolysis leads to a mixture
of 1,16-hexadecanolide and cyclopentadecane. The latter is oxidized by oxygen
under boric acid catalysis to cyclopentadecanol, which is subsequently oxidized
to cyclopentadecanone.
Due to the availability of long-chained aliphatic dicarboxylic acids by biotechnological
processes, a Dieckmann condensation reaction may also possibly
be a useful route to produce this macrocyclic ketone.
Cyclopentadecanone is used in fine fragrances：
Occurrence
Reported to be found in the scent glands of the Louisiana muskrat Ondatra zibethicus rivalicius (Guenther, 1949).
Uses
Cyclopentadecanone is the main odoriferous component of musk.
Preparation
By the cyclization of dinitriles in high dilution (Bedoukian. 1967).
Synthesis Reference(s)
Chemistry Letters, 7, p. 1283, 1978
The Journal of Organic Chemistry, 36, p. 3266, 1971 DOI: 10.1021/jo00821a003
Toxicity evaluation
Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno. 1975). The acute ip LD100 of cyclopentadecanone was not reached but was estimated to be >35mmol/kg for mice; an ip dose of 11-25 mmol/kg caused no deaths in 24 hr and one of 8-92 mmol/kg caused no deaths in 4 days (the length of the study). An oral dose of ≥45 mmol/kg caused no deaths in mice. Intense agitation accompanied by catatonia of the tail was caused by low doses of cyclopentadecanone; gross examination of the mice revealed no specific pathology but occasionally degenerative hepatitis, proximal tubular nephritis and, rarely, pancreatic necrosis were found following dosing with cycloalkanones (Caujolle & Caujolle, 1965).
Flammability and Explosibility
Non flammable
Metabolism
Ketones are not readily metabolized, although most of them probably undergo appreciable reduction to the corresponding secondary alcohols, which are excreted in the urine as glucuronic acid conjugates (Williams, 1959). Cyclopentadecanone was hydroxylated in cultures of four steroid-hydroxylating fungi (Calonectria decora, Rhizopus nigricans, Daedalea rufescens and Ophiobolus herpotrichus), but was not affected by Aspergillus ochraceus. Initial attack occurred at the most remote carbon atom, with yields of up to 26% of 8-hydroxycyclopentadecanone, plus dihydroxy compounds and more polar products (Ashton, Bailey & Jones, 1974).
Purification Methods
Subliming Exaltone is better than crystallising it from aqueous EtOH for purification. The semicarbazone has m 186-187o. [Stevens & Erickson J Am Chem Soc 64 146 1942, Mathur et al. J Chem Soc 3505 1963, Biens & Hess Helv Chim Acta 71 1704 1988, Beilstein 7 III 203, 7 IV 118.]
Cyclopentadecanone Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Cyclopentadecanone manufacturers
- Product
- Cyclopentadecanone 502-72-7
- Price
- US $20.00/kg
- Min. Order
- 1kg
- Purity
- 99.9%
- Supply Ability
- 200000kg
- Release date
- 2024-04-26
- Product
- Cyclopentadecanone 502-72-7
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 0.99
- Supply Ability
- 50000kg
- Release date
- 2023-11-02
- Product
- Cyclopentadecanone 502-72-7
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 50000KG/month
- Release date
- 2023-06-29