CAS 99-83-2|α-phellandrene
Introduction：Basic information about CAS 99-83-2|α-phellandrene, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | α-phellandrene | ||
|---|---|---|---|
| CAS Number | 99-83-2 | Molecular Weight | 136.23 |
| Density | 0.8±0.1 g/cm3 | Boiling Point | 171.5±0.0 °C at 760 mmHg |
| Molecular Formula | C10H16 | Melting Point | / |
| MSDS | ChineseUSA | Flash Point | 43.7±13.0 °C |
| Symbol | GHS02, GHS07, GHS08 | Signal Word | Danger |
Names
| Name | α-phellandrene |
|---|---|
| Synonym | More Synonyms |
α-phellandrene BiologicalActivity
| Description | α-Phellandrene (alpha-Phellandrene) has antifungal activity. α-Phellandrene significantly inhibits the hyphal growth of P. cyclopium, destroys their cell membrane integrity and causes leakage of cellular components[1]. |
|---|---|
| Related Catalog | Research Areas >>InfectionSignaling Pathways >>Anti-infection >>Fungal |
| References | [1]. Zhang JH, et al. Anti-fungal activity, mechanism studies on α-Phellandrene and Nonanal against Penicillium cyclopium. Bot Stud. 2017 Dec;58(1):13. |
Chemical & Physical Properties
| Density | 0.8±0.1 g/cm3 |
|---|---|
| Boiling Point | 171.5±0.0 °C at 760 mmHg |
| Molecular Formula | C10H16 |
| Molecular Weight | 136.23 |
| Flash Point | 43.7±13.0 °C |
| Exact Mass | 136.125198 |
| LogP | 4.43 |
| Vapour Pressure | 1.9±0.1 mmHg at 25°C |
| Index of Refraction | 1.469 |
| InChIKey | OGLDWXZKYODSOB-UHFFFAOYSA-N |
| SMILES | CC1=CCC(C(C)C)C=C1 |
Toxicological Information
CHEMICAL IDENTIFICATION |
ACUTE TOXICITY DATA - TYPE OF TEST :
- Standard Draize test
- ROUTE OF EXPOSURE :
- Administration onto the skin
- SPECIES OBSERVED :
- Human - man
- REFERENCE :
- FCTXAV Food and Cosmetics Toxicology. (London, UK) V.1-19, 1963-81. For publisher information, see FCTOD7. Volume(issue)/page/year: 16,843,1978 ** ACUTE TOXICITY DATA **
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 5700 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- FCTXAV Food and Cosmetics Toxicology. (London, UK) V.1-19, 1963-81. For publisher information, see FCTOD7. Volume(issue)/page/year: 16,843,1978 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X2097 No. of Facilities: 361 (estimated) No. of Industries: 9 No. of Occupations: 8 No. of Employees: 13236 (estimated) No. of Female Employees: 2826 (estimated)
Safety Information
| Symbol | GHS02, GHS07, GHS08 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H226-H302-H315-H319-H334-H335 |
| Precautionary Statements | P261-P305 + P351 + P338-P342 + P311 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | Xn,F |
| Risk Phrases | 10-22-36/37/38-43 |
| Safety Phrases | 16-26-36/37 |
| RIDADR | UN 2319 3 |
| WGK Germany | 3 |
| RTECS | OS8080000 |
| Packaging Group | III |
| Hazard Class | 3.2 |
| HS Code | 2902199090 |
Customs
| HS Code | 2902199090 |
|---|---|
| Summary | 2902199090 other cyclanes, cyclenes and cyclotherpenes。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0% |
Articles11
More Articles| Simple chiral diene ligands provide high enantioselectivities in transition-metal-catalyzed conjugate addition reactions. Org. Lett. 10 , 4387-4389, (2008) Chiral dienes possessing the bicyclo[2.2.2]octadiene framework were prepared readily through the [4 + 2] cycloaddition of ( R)-alpha-phellandrene with methyl propiolate as the key step. Diene 9, subst... | |
| [Study on chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus]. Zhong Yao Cai 32(1) , 67-70, (2009) The chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus were studied.The essential oil was extracted from the stem of A. brachypus by steam distillation, ... | |
| Monoterpenes in the glandular trichomes of tomato are synthesized from a neryl diphosphate precursor rather than geranyl diphosphate. Proc. Natl. Acad. Sci. U. S. A. 106(26) , 10865-70, (2009) We identified a cis-prenyltransferase gene, neryl diphosphate synthase 1 (NDPS1), that is expressed in cultivated tomato (Solanum lycopersicum) cultivar M82 type VI glandular trichomes and encodes an ... |
Synonyms
| (±)-a-Phellandrene |
| 3-Thujylidenehydrazide of isonicotinic acid |
| 2-methyl-5-isopropylcyclohexa-1,3-diene |
| a-phellandrene |
| 5-Isopropyl-2-methylcyclohexa-1,3-diene |
| ISONICOTINIC ACID,3-THUJYLIDENEHYDRAZIDE |
| 5-Isopropyl-2-methyl-1,3-cyclohexadiene |
| alpha-phellandrene |
| MFCD00040419 |
| EINECS 202-792-5 |
| 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethyl)- |
| 2-methyl-5-(propan-2-yl)cyclohexa-1,3-diene |
| (3R,5R)-(+)-2,6-DIMETHYL-3,5-HEPTANEDIOL |
| 2-Methyl-5-isopropyl-3-isonicotinoylhydrazono-bicyclo[3.1.0]hexan |
| Phellandrene |
