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Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer

CAS 25766-18-1C10H16MW 136.23

Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer (CAS 25766-18-1) — formula C10H16, molecular weight 136.23; category paints and coatings.

Product Overview

CAS Number25766-18-1
Molecular FormulaC10H16
Molecular Weight136.23
Melting Point-67 °F (NTP, 1992)
Boiling Point313.2 °F at 760 mmHg (NTP, 1992)
LogP2.8
ApplicationsUses: Used to make camphor, insecticides, solvents, plasticizers, perfume bases, synthetic pine oil, flavorings, geraniol, terpineol, terpene esters and ethers, lube oil additives, camphene, terpin hydrate, and toxaphene, Also used as an odorant for synthetic resins and as a solvent for protective coatings, polishes, and waxes, [HSDB], Painting (Solvents) [Category: Paint], Used to make camphor, and synthetic pine oil, [Merck Index], For alpha-pinene (USEPA, OPP Pesticide Code: 067004) 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., Cosmetics, food, foodstuff additive, odor agents, Mfr of insecticides, former, Flavor ingredient, For more Uses (Complete) data for ALPHA-PINENE (9 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Intermediate, Fragrance, Intermediates, Consumer Uses: Solvent, Household Products: Information on 40 consumer products that contain Alpha-Pinenes in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Methods of Manufacturing: Obtained from oil of turpentine which contains 58-65% alpha-pinene along with 30% beta-pinene., Isolation of d-alpha-pinene from Port Oxford cedar wood oil (Chamaecyparis lawsoniama Parl., Pinaceae) ... Isolation of l-alpha-pinene from mandarin peel oil (Citrus reticulata Blando, Rutaceae)., Pure alpha-pinene is obtained by distillation of turpentine oils., U.S. Production: 2023: 55, 000, 000 - <70, 000 lb, 2022: 55, 2021: 55, 2020: 70, 000 - <85, (1972) 9.0X10+9 GRAMS (SALES), (1976) 2.41X10+9 GRAMS (SALES), alpha-Pinene is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2031], General Manufacturing Information: All Other Basic Organic Chemical Manufacturing, Soap, Cleaning Compound, and Toilet Preparation Manufacturing, Bicyclo[3.1.1]hept-2-ene, 2, 6, 6-trimethyl-: ACTIVE, Epoxidation of alpha-pinene gives pinene oxide which is isomerized to give campholenic aldehyde, an important feedstock for a variety of sandalwood materials., Pyrolysis yields a mixture of ocimene and allocimene
CategoryPaints & Coatings

Applications

Documented applications: Uses: Used to make camphor, insecticides, solvents, plasticizers, perfume bases, synthetic pine oil, flavorings, geraniol, terpineol, terpene esters and ethers, lube oil additives, camphene, terpin hydrate, and toxaphene, Also used as an odorant for synthetic resins and as a solvent for protective coatings, polishes, and waxes, [HSDB], Painting (Solvents) [Category: Paint], Used to make camphor, and synthetic pine oil, [Merck Index], For alpha-pinene (USEPA, OPP Pesticide Code: 067004) 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., Cosmetics, food, foodstuff additive, odor agents, Mfr of insecticides, former, Flavor ingredient, For more Uses (Complete) data for ALPHA-PINENE (9 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Intermediate, Fragrance, Intermediates, Consumer Uses: Solvent, Household Products: Information on 40 consumer products that contain Alpha-Pinenes in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Methods of Manufacturing: Obtained from oil of turpentine which contains 58-65% alpha-pinene along with 30% beta-pinene., Isolation of d-alpha-pinene from Port Oxford cedar wood oil (Chamaecyparis lawsoniama Parl., Pinaceae) ... Isolation of l-alpha-pinene from mandarin peel oil (Citrus reticulata Blando, Rutaceae)., Pure alpha-pinene is obtained by distillation of turpentine oils., U.S. Production: 2023: 55, 000, 000 - <70, 000 lb, 2022: 55, 2021: 55, 2020: 70, 000 - <85, (1972) 9.0X10+9 GRAMS (SALES), (1976) 2.41X10+9 GRAMS (SALES), alpha-Pinene is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2031], General Manufacturing Information: All Other Basic Organic Chemical Manufacturing, Soap, Cleaning Compound, and Toilet Preparation Manufacturing, Bicyclo[3.1.1]hept-2-ene, 2, 6, 6-trimethyl-: ACTIVE, Epoxidation of alpha-pinene gives pinene oxide which is isomerized to give campholenic aldehyde, an important feedstock for a variety of sandalwood materials., Pyrolysis yields a mixture of ocimene and allocimene.

Technical Profile

What this product is

Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer is a coating compound with CAS registry number 25766-18-1 and molecular formula C10H16 (molecular weight 136.23), belonging to the paints and coatings segment of chemical raw materials.

Identification

CAS number: 25766-18-1

Its molecular formula C10H16 comprises 10 C, 16 H atoms.

Also known as: Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer · 双环[3.1.1]庚-2-烯,2,6,6-三甲基-均聚物

Category: paints and coatings

Frequently Asked Questions

What is the CAS number of Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer?

The CAS registry number of Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer is 25766-18-1.

What is the molecular formula and molecular weight of Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer?

Molecular formula C10H16, molecular weight 136.23.

What other names is Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer known by?

It is also registered under: Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer, 双环[3.1.1]庚-2-烯,2,6,6-三甲基-均聚物.

What are the documented applications of Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer?

Recorded applications: Uses: Used to make camphor, insecticides, solvents, plasticizers, perfume bases, synthetic pine oil, flavorings, geraniol, terpineol, terpene esters and ethers, lube oil additives, camphene, terpin hydrate, and toxaphene, Also used as an odorant for synthetic resins and as a solvent for protective coatings, polishes, and waxes, [HSDB], Painting (Solvents) [Category: Paint], Used to make camphor, and synthetic pine oil, [Merck Index], For alpha-pinene (USEPA, OPP Pesticide Code: 067004) 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., Cosmetics, food, foodstuff additive, odor agents, Mfr of insecticides, former, Flavor ingredient, For more Uses (Complete) data for ALPHA-PINENE (9 total), please visit the HSDB record page., Use Classification: Fragrance Ingredients, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Intermediate, Fragrance, Intermediates, Consumer Uses: Solvent, Household Products: Information on 40 consumer products that contain Alpha-Pinenes in the following categories is provided:, • Auto Products, • Commercial, Institutional, • Inside the Home, • Personal Care, Methods of Manufacturing: Obtained from oil of turpentine which contains 58-65% alpha-pinene along with 30% beta-pinene., Isolation of d-alpha-pinene from Port Oxford cedar wood oil (Chamaecyparis lawsoniama Parl., Pinaceae) ... Isolation of l-alpha-pinene from mandarin peel oil (Citrus reticulata Blando, Rutaceae)., Pure alpha-pinene is obtained by distillation of turpentine oils., U.S. Production: 2023: 55, 000, 000 - <70, 000 lb, 2022: 55, 2021: 55, 2020: 70, 000 - <85, (1972) 9.0X10+9 GRAMS (SALES), (1976) 2.41X10+9 GRAMS (SALES), alpha-Pinene is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2031], General Manufacturing Information: All Other Basic Organic Chemical Manufacturing, Soap, Cleaning Compound, and Toilet Preparation Manufacturing, Bicyclo[3.1.1]hept-2-ene, 2, 6, 6-trimethyl-: ACTIVE, Epoxidation of alpha-pinene gives pinene oxide which is isomerized to give campholenic aldehyde, an important feedstock for a variety of sandalwood materials., Pyrolysis yields a mixture of ocimene and allocimene.

Which category does Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer belong to?

Category: Paints & Coatings.

PubChem Public Data

Independent reference data for Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer (CAS 25766-18-1), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number25766-18-1
PubChem CID6654
Molecular formulaC10H16
IUPAC name2,6,6-trimethylbicyclo[3.1.1]hept-2-ene
UNII (FDA)JPF3YI7O34
FEMA number2902
JECFA number1329

Computed descriptors

Molecular Weight136.23
XLogP32.8
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass136.125200510
Monoisotopic Mass136.125200510
Topological Polar Surface Area0
Heavy Atom Count10

Physicochemical values on record

Boiling Point313.2 °F at 760 mmHg (NTP, 1992)
Boiling Point156 °C at 760 mm Hg
Boiling Point155 °C
Boiling Point313.2 °F
Melting Point-67 °F (NTP, 1992)
Melting Point-62.5 °C
Melting Point-67 °F
Flash Point91 °F (NTP, 1992)
Flash Point33 °C
Flash Point91 °F (33 °C) (CLOSED CUP)

Documented uses on record

    Used to make camphor, insecticides, solvents, plasticizers, perfume bases, synthetic pine oil, flavorings, geraniol, terpineol, terpene esters and ethers, lube oil additives, camphene, terpin hydrate, and toxaphene; Also used as an odorant for synthetic resins and as a solvent for protective coatings, polishes, and waxes; [HSDB]Painting (Solvents) [Category: Paint]

    Synonyms and trade names

    ALPHA-PINENE; 80-56-8; 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; Acintene A; pin-2(3)-ene; alfa-Pinene; Sylvapine A; PINENE, ALPHA; DTXSID4026501; Leavo-95; (+-)-alpha-pinene; (+-)-2-pinene; NSC-7727; 2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene; Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-; PC-500(TERPENE)

    Regulatory listings held on file

    Regulatory & Food ContactEU Flavoring substances
    FDA Substance added to food: FLAVORING AGENT OR ADJUVANT
    FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS
    Flavoring Agents
    FLAVOURING_AGENT: Flavouring Agent
    Cedarwood, Pine, Sharp
    GHS notification summary1.2% (25 / 2036)

    GHS hazard classification

    GHS notification summary1.2% (25 / 2036)
    Reported hazard statementsH226 (97.6%), H302 (13.7%), H304 (74.1%), H315 (83.2%), H317 (66.1%), H318 (23.3%), H400 (52.7%), H410 (55.7%)

    This chemical does not meet GHS hazard criteria for 1.2% (25 of 2036) of reports.

    H226 (97.6%): Flammable liquid and vapor [Warning Flammable liquids]

    What the public record says

    Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-, homopolymer · CAS 25766-18-1 · C10H16. UNII JPF3YI7O34. Boiling Point: 313.2 °F at 760 mmHg (NTP, 1992); Boiling Point: 156 °C at 760 mm Hg; Boiling Point: 155 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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中文页面: 双环[3.1.1]庚-2-烯,2,6,6-三甲基-均聚物

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