Isobornyl acetate
- CAS No.
- 125-12-2
- Chemical Name:
- Isobornyl acetate
- Synonyms
- Isobornyl;Isomethyl lonone;Pichtosine;2-CAMPHANYL ACETATE;D,L-ISOBORNYL ACETATE;1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate;exo-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate;Nsc62486;FEMA 2160;Pichtosin
- CBNumber:
- CB0358907
- Molecular Formula:
- C12H20O2
- Molecular Weight:
- 196.29
- MOL File:
- 125-12-2.mol
- Modify Date:
- 2024/5/29 17:48:59
| Melting point | 29°C |
|---|---|
| Boiling point | 229-233 °C (lit.) |
| Density | 0.983 g/mL at 25 °C (lit.) |
| vapor pressure | 0.13 hPa (20 °C) |
| FEMA | 2160 | ISOBORNYL ACETATE |
| refractive index |
n |
| Flash point | 190 °F |
| storage temp. | Store below +30°C. |
| solubility | 0.16g/l |
| form | Oil |
| color | Colourless |
| Specific Gravity | 0.98 |
| Odor | at 100.00 %. balsam camphor herbal woody sweet |
| Odor Type | balsamic |
| Water Solubility | Not miscible or difficult to mix with water. |
| JECFA Number | 1388 |
| BRN | 3197572 |
| Stability | Stable. Flammable. Incompatible with strong oxidizing agents. |
| InChIKey | XWIGWPJZNFZLBG-UHFFFAOYSA-N |
| LogP | 3.86 |
| CAS DataBase Reference | 125-12-2(CAS DataBase Reference) |
| NIST Chemistry Reference | Isobornyl acetate(125-12-2) |
| EPA Substance Registry System | Isobornyl acetate (125-12-2) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H315 | |||||||||
| Precautionary statements | P264-P280-P302+P352-P332+P313-P362+P364 | |||||||||
| Hazard Codes | Xi | |||||||||
| Risk Statements | 36/37/38-38 | |||||||||
| Safety Statements | 26-36/37/39-24/25 | |||||||||
| WGK Germany | 1 | |||||||||
| RTECS | NP7350000 | |||||||||
| Autoignition Temperature | 440 °C DIN 51794 | |||||||||
| TSCA | Yes | |||||||||
| HS Code | 29153900 | |||||||||
| Toxicity | LD50 orally in Rabbit: > 10000 mg/kg LD50 dermal Rabbit > 20000 mg/kg | |||||||||
| NFPA 704 |
|
Isobornyl acetate price More Price(8)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | W216003 | Isobornyl acetate | 125-12-2 | 1SAMPLE-K | ₹5141.88 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W216003 | Isobornyl acetate | 125-12-2 | 1KG | ₹7804.83 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W216003 | Isobornyl acetate | 125-12-2 | 10KG | ₹18911.28 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W216003 | Isobornyl acetate | 125-12-2 | 25KG | ₹30136.8 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | 8.14998 | Isobornyl acetate for synthesis | 125-12-2 | 250ML | ₹3030 | 2022-06-14 | Buy |
Isobornyl acetate Chemical Properties,Uses,Production
Description
Isobornyl acetate has a pleasant, camphor-like odor reminiscent of some varieties of pine needles and hemlock, and a fresh, burning taste. May be prepared by treatment of camphene with acetic acid, usually in the presence of a catalyst; also by acetylation of isobomeol; depending on the starting material (d-camphene or ι-camphene), the resulting acetate may exhibit a slight optical activity; the commercial product is considered to be optically inactive.
Chemical Properties
Isobornyl Acetate has
been identified in a number of essential oils. It is a colorless liquid with a pleasant, pine-needle odor. Isobornyl acetate is prepared from camphene and
acetic acid in the presence of acidic catalysts (e.g., sulfuric acid) or on a
styrene–divinylbenzene acid ion-exchanger.
Isobornyl acetate is used in large amounts for perfuming soaps, bath products,
and air fresheners. However, the major use of isobornyl acetate is as an intermediate
in the production of camphor.
Occurrence
Reported found in thymus, Parmesan cheese, dill herb, Ocimum basilicum, rosemary and custard apple
Uses
Isobornyl acetate is one of the most important chemicals used in the perfumery industry. It is used in toiletries and soaps as a flavoring agent and antiseptics. One of main applications is as an intermediate to produce camphor.
Preparation
By treatment of camphene with acetic acid, usually in the presence of a catalyst; also by acetylation of isoborneol; depending on the starting material (d-camphene or l-camphene), the resulting acetate may exhibit slight optical activity; the commercial product is considered to be optically inactive
Isobornyl acetate Preparation Products And Raw materials
Raw materials
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chevron_rightPreparation Products
| Supplier | Tel | Country | ProdList | Advantage | Inquiry |
|---|---|---|---|---|---|
| HJ AROCHEM | +91-8690768060 +91-9724420086 | Ahmedabad, India | 171 | 58 | Inquiry |
| Neeru Menthol Pvt Ltd | +91-8884114465 +91-9837322285 | New Delhi, India | 70 | 58 | Inquiry |
| Mruchem | +91-8087147166 +91-8087147166 | Gujarat, India | 52 | 58 | Inquiry |
| Desicca Chemicals | +91-7777090620 +91-9821128366 | Maharashtra, India | 20 | 58 | Inquiry |
| Privi Speciality Chemicals Ltd. | +91-2233043500 +91-2233043500 | Mumbai, India | 63 | 58 | Inquiry |
| Oriental Aromatics Ltd | +91-2243214000 +91-2266556000 | Maharashtra, India | 33 | 58 | Inquiry |
| Jay Chem Marketing | 08048964412 | Mumbai, India | 231 | 58 | Inquiry |
| Global Flavors and Fragrances | +91-22-2407 7476 | Mumbai, India | 45 | 58 | Inquiry |
| S H Kelkar and Company Limited | 91-22-22069609 | Maharashtra, India | 62 | 58 | Inquiry |
| Rawji Fine Fragrances Pvt., Ltd. | 91-22-23445455 | Maharashtra, India | 21 | 58 | Inquiry |
| Supplier | Advantage |
|---|---|
| HJ AROCHEM | 58 |
| Neeru Menthol Pvt Ltd | 58 |
| Mruchem | 58 |
| Desicca Chemicals | 58 |
| Privi Speciality Chemicals Ltd. | 58 |
| Oriental Aromatics Ltd | 58 |
| Jay Chem Marketing | 58 |
| Global Flavors and Fragrances | 58 |
| S H Kelkar and Company Limited | 58 |
| Rawji Fine Fragrances Pvt., Ltd. | 58 |
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