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(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇

CAS 10334-13-1C10H18OMW 154.25

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇(CAS 10334-13-1):分子式 C10H18O、分子量 154.25。

产品概览

CAS号10334-13-1
分子式C10H18O
分子量154.25
熔点216 °C
LogPlog Kow = 3.24
应用领域Uses: Used as a synthetic flavor、In over-the-counter preparations containing <11% camphor、it has been used as a moth repellent、cold sore topical medication、muscle liniment、and steam-inhaled cough suppressant、[HSDB] Used in perfumes、[Hawley]、For isoborneol (USEPA、OPP Pesticide Code: 047089) 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.、Reported uses (ppm):、Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#4225]、Perfumery、chemical esters.、The repellence of the plant-derived bicyclic monoterpenoid isoborneol on subterranean termites was assessed in short-term laboratory bioassays. Depending on concentration、application of isoborneol to different soil types was efficient in creating repellent soil barriers、which were not penetrated by workers of Reticulitermes santonensis De Feytaud or R. flavipes Kollar within 2 wk after adding the substance to the substrate. Isoborneol-treated barriers did not affect termite survival. The bioavailability of the active ingredient decreased with increasing clay content of the soil. Evaporation of isoborneol from treated soil increased with increasing particle size of the substrate and could be reduced by covering the soil surface.、MEDICATION、Use Classification: Fragrance Ingredients、Flavoring Agents -> JECFA Flavorings Index、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Industry Uses: Other、Fragrance、Consumer Uses: Fragrance、Household Products: Information on 6 consumer products that contain Isoborneol in the following categories is provided:、• Commercial、Institutional、• Inside the Home、Methods of Manufacturing: By hydrolysis of isobornyl acetate、or by catalytic reduction of camphor (both d- and l-isomers)、the optically inactive compound can be prepared by treating camphene with 1:1 mixture of sulfuric acid and glacial acetic acid and then hydrolyzing the isobornyl acetate.、U.S. Production: 2023: 250、000 - <400、000 lb、2022: 250、2021: 250、2020: 50、000 - <250、Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Isoborneol:、Table: National Aggregate Production Volume (pounds) [Table#4224]、General Manufacturing Information: All Other Chemical Product and Preparation Manufacturing、Not Known or Reasonably Ascertainable、Plastics Material and Resin Manufacturing、Soap、Cleaning Compound、and Toilet Preparation Manufacturing、Bicyclo[2.2.1]heptan-2-ol、1、7、7-trimethyl-、(1R、2R、4R)-rel-: ACTIVE、Borneol is an endo isomer、the corresponding exo isomer is isoborneol、Natural occurrence: Ashanti pepper (Piper guineense Schum and Thom) Ginger (Zingiber species) Grape brandy Camomile Honey Cheese、various types Mastic (Pistacia lentiscus) Cinnamomum species Ocimum species Curcuma species Papaya (Carica papaya L.) Eucalyptus oil (Eucalyptus globulus Labill) Raspberry、blackberry and boysenberry Rooibos tea (Aspalathus linearis) Salvia species Rosemary (Rosmarinus officinalis L.) Thyme (Thymus species)

应用领域

登记用途:Uses: Used as a synthetic flavor、In over-the-counter preparations containing <11% camphor、it has been used as a moth repellent、cold sore topical medication、muscle liniment、and steam-inhaled cough suppressant、[HSDB] Used in perfumes、[Hawley]、For isoborneol (USEPA、OPP Pesticide Code: 047089) 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.、Reported uses (ppm):、Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#4225]、Perfumery、chemical esters.、The repellence of the plant-derived bicyclic monoterpenoid isoborneol on subterranean termites was assessed in short-term laboratory bioassays. Depending on concentration、application of isoborneol to different soil types was efficient in creating repellent soil barriers、which were not penetrated by workers of Reticulitermes santonensis De Feytaud or R. flavipes Kollar within 2 wk after adding the substance to the substrate. Isoborneol-treated barriers did not affect termite survival. The bioavailability of the active ingredient decreased with increasing clay content of the soil. Evaporation of isoborneol from treated soil increased with increasing particle size of the substrate and could be reduced by covering the soil surface.、MEDICATION、Use Classification: Fragrance Ingredients、Flavoring Agents -> JECFA Flavorings Index、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Industry Uses: Other、Fragrance、Consumer Uses: Fragrance、Household Products: Information on 6 consumer products that contain Isoborneol in the following categories is provided:、• Commercial、Institutional、• Inside the Home、Methods of Manufacturing: By hydrolysis of isobornyl acetate、or by catalytic reduction of camphor (both d- and l-isomers)、the optically inactive compound can be prepared by treating camphene with 1:1 mixture of sulfuric acid and glacial acetic acid and then hydrolyzing the isobornyl acetate.、U.S. Production: 2023: 250、000 - <400、000 lb、2022: 250、2021: 250、2020: 50、000 - <250、Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Isoborneol:、Table: National Aggregate Production Volume (pounds) [Table#4224]、General Manufacturing Information: All Other Chemical Product and Preparation Manufacturing、Not Known or Reasonably Ascertainable、Plastics Material and Resin Manufacturing、Soap、Cleaning Compound、and Toilet Preparation Manufacturing、Bicyclo[2.2.1]heptan-2-ol、1、7、7-trimethyl-、(1R、2R、4R)-rel-: ACTIVE、Borneol is an endo isomer、the corresponding exo isomer is isoborneol、Natural occurrence: Ashanti pepper (Piper guineense Schum and Thom) Ginger (Zingiber species) Grape brandy Camomile Honey Cheese、various types Mastic (Pistacia lentiscus) Cinnamomum species Ocimum species Curcuma species Papaya (Carica papaya L.) Eucalyptus oil (Eucalyptus globulus Labill) Raspberry、blackberry and boysenberry Rooibos tea (Aspalathus linearis) Salvia species Rosemary (Rosmarinus officinalis L.) Thyme (Thymus species)。

技术档案

这个产品是什么

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 是一种化工化合物,登记 CAS 号为 10334-13-1,分子式 C10H18O(分子量 154.25)。

识别信息

登记 CAS 号:10334-13-1

其分子式 C10H18O 由 10 个碳、18 个氢、1 个氧 组成。

别名/同义词:(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 · (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2α-ol

常见问题

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 的 CAS 号是多少?

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 的 CAS 登记号为 10334-13-1。

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 的分子式与分子量是多少?

分子式 C10H18O,分子量 154.25。

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 还有哪些别名?

别名/同义词:(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇、(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2α-ol。

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 的登记用途是什么?

登记用途:Uses: Used as a synthetic flavor、In over-the-counter preparations containing <11% camphor、it has been used as a moth repellent、cold sore topical medication、muscle liniment、and steam-inhaled cough suppressant、[HSDB] Used in perfumes、[Hawley]、For isoborneol (USEPA、OPP Pesticide Code: 047089) 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.、Reported uses (ppm):、Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#4225]、Perfumery、chemical esters.、The repellence of the plant-derived bicyclic monoterpenoid isoborneol on subterranean termites was assessed in short-term laboratory bioassays. Depending on concentration、application of isoborneol to different soil types was efficient in creating repellent soil barriers、which were not penetrated by workers of Reticulitermes santonensis De Feytaud or R. flavipes Kollar within 2 wk after adding the substance to the substrate. Isoborneol-treated barriers did not affect termite survival. The bioavailability of the active ingredient decreased with increasing clay content of the soil. Evaporation of isoborneol from treated soil increased with increasing particle size of the substrate and could be reduced by covering the soil surface.、MEDICATION、Use Classification: Fragrance Ingredients、Flavoring Agents -> JECFA Flavorings Index、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Industry Uses: Other、Fragrance、Consumer Uses: Fragrance、Household Products: Information on 6 consumer products that contain Isoborneol in the following categories is provided:、• Commercial、Institutional、• Inside the Home、Methods of Manufacturing: By hydrolysis of isobornyl acetate、or by catalytic reduction of camphor (both d- and l-isomers)、the optically inactive compound can be prepared by treating camphene with 1:1 mixture of sulfuric acid and glacial acetic acid and then hydrolyzing the isobornyl acetate.、U.S. Production: 2023: 250、000 - <400、000 lb、2022: 250、2021: 250、2020: 50、000 - <250、Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Isoborneol:、Table: National Aggregate Production Volume (pounds) [Table#4224]、General Manufacturing Information: All Other Chemical Product and Preparation Manufacturing、Not Known or Reasonably Ascertainable、Plastics Material and Resin Manufacturing、Soap、Cleaning Compound、and Toilet Preparation Manufacturing、Bicyclo[2.2.1]heptan-2-ol、1、7、7-trimethyl-、(1R、2R、4R)-rel-: ACTIVE、Borneol is an endo isomer、the corresponding exo isomer is isoborneol、Natural occurrence: Ashanti pepper (Piper guineense Schum and Thom) Ginger (Zingiber species) Grape brandy Camomile Honey Cheese、various types Mastic (Pistacia lentiscus) Cinnamomum species Ocimum species Curcuma species Papaya (Carica papaya L.) Eucalyptus oil (Eucalyptus globulus Labill) Raspberry、blackberry and boysenberry Rooibos tea (Aspalathus linearis) Salvia species Rosemary (Rosmarinus officinalis L.) Thyme (Thymus species)。

PubChem 公开数据

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇(CAS 10334-13-1)的独立参考数据,整理自公开化学数据库。

各数据库的登记标识

CAS 号10334-13-1
PubChem CID6321405
分子式C10H18O
IUPAC 名称(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
UNII(FDA)L88RA8N5EG
FEMA 编号2158
JECFA 编号1386

计算分子描述符

Molecular Weight154.25
XLogP32.7
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass154.135765193
Monoisotopic Mass154.135765193
Topological Polar Surface Area20.2
Heavy Atom Count11

在册的理化数值

Melting Point216 °C
Melting Point212 °C
Density1.10 g/cm cu at 20 °C
Vapor Pressure0.03 [mmHg]
LogPlog Kow = 3.24

同义词与商品名

Isoborneol; 124-76-5; Isocamphol; Isobornyl alcohol; 2-exo-Bornyl alcohol; Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel-; FEMA No. 2158; DTXSID2042060; L88RA8N5EG; DTXCID0022060; NSC-26350; Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel-; RefChem:5910; 204-712-4; (-)-Isoborneol; DL-Isoborneol

已收录的法规名录

法规与食品接触EU Flavoring substances
FDA Substance added to food: FLAVORING AGENT OR ADJUVANT
Flavoring Agents
FLAVOURING_AGENT: Flavouring Agent
Camphor, Must
No safety concern at current levels of intake when used as a flavouring agent

GHS 危害分类

已通报的危害声明H228 (99.6%), H315 (11.4%)

公开数据库对它的描述

(1R,4R)-1,7,7-三甲基双环[2.2.1]庚-2α-醇 · CAS 10334-13-1 · C10H18O. UNII L88RA8N5EG. Melting Point: 216 °C; Melting Point: 212 °C; Density: 1.10 g/cm cu at 20 °C.

数据来源:PubChem / Wikidata;与随货 COA 不一致时以 COA 为准。

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