TURPENTINE OIL (CAS 7705-14-8) — formula C10H16, molecular weight 136.23; category food flavors.
| CAS Number | 7705-14-8 |
|---|---|
| Molecular Formula | C10H16 |
| Molecular Weight | 136.23 |
| Melting Point | -40 °F (USCG, 1999) |
| Boiling Point | 352 °F at 760 mmHg (USCG, 1999) |
| LogP | 3.4 |
| Applications | Uses: Used in flavorings, fragrances, cosmetics and as a solvent and wetting agent, Also used to make resins, insecticides, insect repellants, and animal repellants, [HSDB] Used as a dissolving agent for gallstones and gutta-percha, [ChemIDplus] Used in floor waxes and furniture polishes, [CAMEO] Occurs naturally in essential oils of many plants and is a minor constituent of turpentine, [CHEMINFO], Painting (Solvents) [Category: Paint], For limonene (USEPA, OPP Pesticide Code: 079701) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Monomer in terpene resins, solvent for oleoresinous products, general wetting and dispersing agent, chemical intermediate for various organic compounds, flavor ingredient (orange-like)., One important use for (R)-(+)-limonene is its use as a chiral starting material for the synthesis of (R)-(-)-carvone., An application for printed circuit board cleaners has also been developed using dipentene and limonene with emulsifying surfactants to facilitate removal by rinsing in water., For more Uses (Complete) data for LIMONENE (13 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Fragrance Ingredients, Cosmetics -> Solvent, Industry Uses: Monomers, Intermediates, Fragrance, Not Known or Reasonably Ascertainable, Soil amendments (fertilizers), Consumer Uses: Fragrance, Household Products: Cosmetics product ingredient: Limonene (1-methyl-4-prop-1-en-2-yl-cyclohexene, dl-limonene (racemic), Dipentene, (R)-p-mentha-1, 8-diene, (d-limonene), (S)-p-mentha-1, (l-limonene)), Limonene is a fragrance allergen. Fragrance allergens are hazardous only to individuals who suffer from fragrance allergies. The Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 requires fragrance allergens included in Annex III of the EU Cosmetics Regulation No. 1223, 2009 be reported to the California Department of Public Health. Fragrance allergens are only required to be reported if present in a rinse-off cosmetic product at a concentration at or above 0.01 percent (100 parts per million) or in a leave-on cosmetic product at a concentration at or above 0.001 percent (10 parts per million)., For more information, you can visit the fragrance allergens webpage on the California Safe Cosmetics Program website:, https:, www.cdph.ca.gov, Programs, CCDPHP, DEODC, OHB, CSCP, Pages, FragranceAllergens.aspx, Product count: 43730, Information on 149 consumer products that contain Dipentene in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Information on 6 consumer products that contain 1-Methyl-4-Methylvinyl-Cyclohexene in the following categories is provided:, Methods of Manufacturing: Extraction from Southeastern pine stumps, and citrus fruits (especially from the peels of oranges and lemons), from pyrolysis of alpha-pinene, As a by-product in the manufacture of terpineol and in various synthetic products made from alpha-pinene or turpentine oil., Derivation: (1) Lemon, bergamot, caraway, orange, and other oils, (2) peppermint and spearmint oils., The richest sources are the oils contained in the peel of citrus fruits, which contain levels up to 90%. The major source of limonene is ... from citrus peel, largely as a by-product of the fruit juice industry. Citrus fruit produce the (R)-enantiomer and so the bulk of commercially available limonene is dextrorotatory. The levorotatory enantiomer is available, but in much more restricted supply and at a higher price., Impurities: Impurities are mainly other monoterpenes, such as myrcene (7-methyl-3-methylene-1, 6-octadiene), alpha-pinene (2, 6, 6-trimethyl-bicyclo[3.1.1]hept-2-ene), alpha-pinene (6, 6-dimethyl-2-methylene-bicyclo[3.1.1]heptane), sabinene (2-methyl-5-(1-methylethyl)-bicyclo[3.1.0]hexan-2-ol), and Gamma3-carene ((1S-cis)-3, 7, 7-trimethyl-bicyclo[4.1.0]hept-2-ene)., Formulations, Preparations: Dipenten, mixture of limonene, 56-64%, and terpinolene, 20-25%, Consumption Patterns: Use in fragrances in the USA amounts to <1000 lb, yr., U.S. Production: 2023: 5, 500, 000 - <7, 000, 000 lb, 2022: 8, 000 - <10, 2021: 8, 2020: 7, 000 - <8, (1986) >10 million-50 million pounds, (1990) 10 thousand-500 thousand pounds, (1994) 10 thousand-500 thousand pounds, (1998) >1 million-10 million pounds, For more U.S. Production (Complete) data for LIMONENE (7 total), General Manufacturing Information: Soap, Cleaning Compound, and Toilet Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Plastics Material and Resin Manufacturing, Cyclohexene, 1-methyl-4-(1-methylethenyl)-: ACTIVE, Concentration in final product (%): as usual to maximum range is 0.05-0.75 in soap, 0.05-0.075 in detergent, 0.5-2.0 in perfume and 0.25 maximum in creams and lotions., A widely distributed, optically active terpene, closely related to isoprene. It occurs naturally in both d- and l-forms. Racemic mixture of the two isomers is known as dipentene., Limonene is the most important and widespread terpene, it is known in the d- and l- optically active forms and in the optically inactive dl-form (known as dipentene). |
| Category | Spice Oils |
Documented applications: Uses: Used in flavorings, fragrances, cosmetics and as a solvent and wetting agent, Also used to make resins, insecticides, insect repellants, and animal repellants, [HSDB] Used as a dissolving agent for gallstones and gutta-percha, [ChemIDplus] Used in floor waxes and furniture polishes, [CAMEO] Occurs naturally in essential oils of many plants and is a minor constituent of turpentine, [CHEMINFO], Painting (Solvents) [Category: Paint], For limonene (USEPA, OPP Pesticide Code: 079701) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Monomer in terpene resins, solvent for oleoresinous products, general wetting and dispersing agent, chemical intermediate for various organic compounds, flavor ingredient (orange-like)., One important use for (R)-(+)-limonene is its use as a chiral starting material for the synthesis of (R)-(-)-carvone., An application for printed circuit board cleaners has also been developed using dipentene and limonene with emulsifying surfactants to facilitate removal by rinsing in water., For more Uses (Complete) data for LIMONENE (13 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Fragrance Ingredients, Cosmetics -> Solvent, Industry Uses: Monomers, Intermediates, Fragrance, Not Known or Reasonably Ascertainable, Soil amendments (fertilizers), Consumer Uses: Fragrance, Household Products: Cosmetics product ingredient: Limonene (1-methyl-4-prop-1-en-2-yl-cyclohexene, dl-limonene (racemic), Dipentene, (R)-p-mentha-1, 8-diene, (d-limonene), (S)-p-mentha-1, (l-limonene)), Limonene is a fragrance allergen. Fragrance allergens are hazardous only to individuals who suffer from fragrance allergies. The Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 requires fragrance allergens included in Annex III of the EU Cosmetics Regulation No. 1223, 2009 be reported to the California Department of Public Health. Fragrance allergens are only required to be reported if present in a rinse-off cosmetic product at a concentration at or above 0.01 percent (100 parts per million) or in a leave-on cosmetic product at a concentration at or above 0.001 percent (10 parts per million)., For more information, you can visit the fragrance allergens webpage on the California Safe Cosmetics Program website:, https:, www.cdph.ca.gov, Programs, CCDPHP, DEODC, OHB, CSCP, Pages, FragranceAllergens.aspx, Product count: 43730, Information on 149 consumer products that contain Dipentene in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Information on 6 consumer products that contain 1-Methyl-4-Methylvinyl-Cyclohexene in the following categories is provided:, Methods of Manufacturing: Extraction from Southeastern pine stumps, and citrus fruits (especially from the peels of oranges and lemons), from pyrolysis of alpha-pinene, As a by-product in the manufacture of terpineol and in various synthetic products made from alpha-pinene or turpentine oil., Derivation: (1) Lemon, bergamot, caraway, orange, and other oils, (2) peppermint and spearmint oils., The richest sources are the oils contained in the peel of citrus fruits, which contain levels up to 90%. The major source of limonene is ... from citrus peel, largely as a by-product of the fruit juice industry. Citrus fruit produce the (R)-enantiomer and so the bulk of commercially available limonene is dextrorotatory. The levorotatory enantiomer is available, but in much more restricted supply and at a higher price., Impurities: Impurities are mainly other monoterpenes, such as myrcene (7-methyl-3-methylene-1, 6-octadiene), alpha-pinene (2, 6, 6-trimethyl-bicyclo[3.1.1]hept-2-ene), alpha-pinene (6, 6-dimethyl-2-methylene-bicyclo[3.1.1]heptane), sabinene (2-methyl-5-(1-methylethyl)-bicyclo[3.1.0]hexan-2-ol), and Gamma3-carene ((1S-cis)-3, 7, 7-trimethyl-bicyclo[4.1.0]hept-2-ene)., Formulations, Preparations: Dipenten, mixture of limonene, 56-64%, and terpinolene, 20-25%, Consumption Patterns: Use in fragrances in the USA amounts to <1000 lb, yr., U.S. Production: 2023: 5, 500, 000 - <7, 000, 000 lb, 2022: 8, 000 - <10, 2021: 8, 2020: 7, 000 - <8, (1986) >10 million-50 million pounds, (1990) 10 thousand-500 thousand pounds, (1994) 10 thousand-500 thousand pounds, (1998) >1 million-10 million pounds, For more U.S. Production (Complete) data for LIMONENE (7 total), General Manufacturing Information: Soap, Cleaning Compound, and Toilet Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Plastics Material and Resin Manufacturing, Cyclohexene, 1-methyl-4-(1-methylethenyl)-: ACTIVE, Concentration in final product (%): as usual to maximum range is 0.05-0.75 in soap, 0.05-0.075 in detergent, 0.5-2.0 in perfume and 0.25 maximum in creams and lotions., A widely distributed, optically active terpene, closely related to isoprene. It occurs naturally in both d- and l-forms. Racemic mixture of the two isomers is known as dipentene., Limonene is the most important and widespread terpene, it is known in the d- and l- optically active forms and in the optically inactive dl-form (known as dipentene)..
TURPENTINE OIL is a flavoring compound with CAS registry number 7705-14-8 and molecular formula C10H16 (molecular weight 136.23), belonging to the food flavors segment of chemical raw materials.
CAS number: 7705-14-8
Its molecular formula C10H16 comprises 10 C, 16 H atoms.
Also known as: TURPENTINE OIL · 松节油
Category: food flavors
The CAS registry number of TURPENTINE OIL is 7705-14-8.
Molecular formula C10H16, molecular weight 136.23.
It is also registered under: TURPENTINE OIL, 松节油.
Recorded applications: Uses: Used in flavorings, fragrances, cosmetics and as a solvent and wetting agent, Also used to make resins, insecticides, insect repellants, and animal repellants, [HSDB] Used as a dissolving agent for gallstones and gutta-percha, [ChemIDplus] Used in floor waxes and furniture polishes, [CAMEO] Occurs naturally in essential oils of many plants and is a minor constituent of turpentine, [CHEMINFO], Painting (Solvents) [Category: Paint], For limonene (USEPA, OPP Pesticide Code: 079701) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Monomer in terpene resins, solvent for oleoresinous products, general wetting and dispersing agent, chemical intermediate for various organic compounds, flavor ingredient (orange-like)., One important use for (R)-(+)-limonene is its use as a chiral starting material for the synthesis of (R)-(-)-carvone., An application for printed circuit board cleaners has also been developed using dipentene and limonene with emulsifying surfactants to facilitate removal by rinsing in water., For more Uses (Complete) data for LIMONENE (13 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Fragrance Ingredients, Cosmetics -> Solvent, Industry Uses: Monomers, Intermediates, Fragrance, Not Known or Reasonably Ascertainable, Soil amendments (fertilizers), Consumer Uses: Fragrance, Household Products: Cosmetics product ingredient: Limonene (1-methyl-4-prop-1-en-2-yl-cyclohexene, dl-limonene (racemic), Dipentene, (R)-p-mentha-1, 8-diene, (d-limonene), (S)-p-mentha-1, (l-limonene)), Limonene is a fragrance allergen. Fragrance allergens are hazardous only to individuals who suffer from fragrance allergies. The Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 requires fragrance allergens included in Annex III of the EU Cosmetics Regulation No. 1223, 2009 be reported to the California Department of Public Health. Fragrance allergens are only required to be reported if present in a rinse-off cosmetic product at a concentration at or above 0.01 percent (100 parts per million) or in a leave-on cosmetic product at a concentration at or above 0.001 percent (10 parts per million)., For more information, you can visit the fragrance allergens webpage on the California Safe Cosmetics Program website:, https:, www.cdph.ca.gov, Programs, CCDPHP, DEODC, OHB, CSCP, Pages, FragranceAllergens.aspx, Product count: 43730, Information on 149 consumer products that contain Dipentene in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Information on 6 consumer products that contain 1-Methyl-4-Methylvinyl-Cyclohexene in the following categories is provided:, Methods of Manufacturing: Extraction from Southeastern pine stumps, and citrus fruits (especially from the peels of oranges and lemons), from pyrolysis of alpha-pinene, As a by-product in the manufacture of terpineol and in various synthetic products made from alpha-pinene or turpentine oil., Derivation: (1) Lemon, bergamot, caraway, orange, and other oils, (2) peppermint and spearmint oils., The richest sources are the oils contained in the peel of citrus fruits, which contain levels up to 90%. The major source of limonene is ... from citrus peel, largely as a by-product of the fruit juice industry. Citrus fruit produce the (R)-enantiomer and so the bulk of commercially available limonene is dextrorotatory. The levorotatory enantiomer is available, but in much more restricted supply and at a higher price., Impurities: Impurities are mainly other monoterpenes, such as myrcene (7-methyl-3-methylene-1, 6-octadiene), alpha-pinene (2, 6, 6-trimethyl-bicyclo[3.1.1]hept-2-ene), alpha-pinene (6, 6-dimethyl-2-methylene-bicyclo[3.1.1]heptane), sabinene (2-methyl-5-(1-methylethyl)-bicyclo[3.1.0]hexan-2-ol), and Gamma3-carene ((1S-cis)-3, 7, 7-trimethyl-bicyclo[4.1.0]hept-2-ene)., Formulations, Preparations: Dipenten, mixture of limonene, 56-64%, and terpinolene, 20-25%, Consumption Patterns: Use in fragrances in the USA amounts to <1000 lb, yr., U.S. Production: 2023: 5, 500, 000 - <7, 000, 000 lb, 2022: 8, 000 - <10, 2021: 8, 2020: 7, 000 - <8, (1986) >10 million-50 million pounds, (1990) 10 thousand-500 thousand pounds, (1994) 10 thousand-500 thousand pounds, (1998) >1 million-10 million pounds, For more U.S. Production (Complete) data for LIMONENE (7 total), General Manufacturing Information: Soap, Cleaning Compound, and Toilet Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Plastics Material and Resin Manufacturing, Cyclohexene, 1-methyl-4-(1-methylethenyl)-: ACTIVE, Concentration in final product (%): as usual to maximum range is 0.05-0.75 in soap, 0.05-0.075 in detergent, 0.5-2.0 in perfume and 0.25 maximum in creams and lotions., A widely distributed, optically active terpene, closely related to isoprene. It occurs naturally in both d- and l-forms. Racemic mixture of the two isomers is known as dipentene., Limonene is the most important and widespread terpene, it is known in the d- and l- optically active forms and in the optically inactive dl-form (known as dipentene)..
Category: Spice Oils.
Independent reference data for TURPENTINE OIL (CAS 7705-14-8), compiled from public chemistry databases.
| CAS Registry Number | 7705-14-8 |
|---|---|
| PubChem CID | 22311 |
| Molecular formula | C10H16 |
| IUPAC name | 1-methyl-4-prop-1-en-2-ylcyclohexene |
| UNII (FDA) | 9MC3I34447 |
| Molecular Weight | 136.23 |
|---|---|
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 1 |
| Exact Mass | 136.125200510 |
| Monoisotopic Mass | 136.125200510 |
| Topological Polar Surface Area | 0 |
| Heavy Atom Count | 10 |
| Boiling Point | 352 °F at 760 mmHg (USCG, 1999) |
|---|---|
| Boiling Point | 352 °F |
| Melting Point | -40 °F (USCG, 1999) |
| Melting Point | -95.5 °C |
| Melting Point | -40 °F |
| Flash Point | 115 °F (USCG, 1999) |
| Flash Point | 45 °C |
| Flash Point | 113 °F (45 °C) (Close cup) |
| Flash Point | 115 °F |
| Solubility | In water, 7.57 mg/L at 25 °C |
1-methyl-4-prop-1-en-2-ylcyclohexene; RefChem:1055817; LIMONENE; Dipentene; 138-86-3; Cinene; Cajeputene; DL-Limonene; Kautschin; Dipenten; Eulimen; Nesol; Limonen; p-Mentha-1,8-diene; 1,8-p-Menthadiene; Cajeputen
| Regulatory & Food Contact | EU Flavoring substances FDA Substance added to food: Use unspecified FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS Flavoring Agents CIR / INCI: Cosmetics ingredient -> Base; Colorant; Conditioning/Emollient; Emulsifier; Flavor; Fragrance; Moisturizing/Hu |
|---|---|
| GHS notification summary | 0.1% (1 / 3461) |
| GHS notification summary | 0.1% (1 / 3461) |
|---|---|
| Reported hazard statements | H226, H315, H317, H400, H410, H304 (49.2%), H319 (14.9%) |
H226: Flammable liquid and vapor [Warning Flammable liquids]
H315: Causes skin irritation [Warning Skin corrosion/irritation]
TURPENTINE OIL · CAS 7705-14-8 · C10H16. UNII 9MC3I34447. Boiling Point: 352 °F at 760 mmHg (USCG, 1999); Boiling Point: 352 °F; Melting Point: -40 °F (USCG, 1999).
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 松节油