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二苯甲酮

CAS 119-61-9C13H10OMW 182.22主营产品

二苯甲酮(CAS 119-61-9):分子式 C13H10O、分子量 182.22;类别 医药中间体。

产品概览

CAS号119-61-9
分子式C13H10O
分子量182.22
熔点47.8
沸点582.6 °F at 760 mmHg (NTP, 1992)
LogP3.4
应用领域Uses: Used in perfumes、flavoring agents、and organic synthesis、Also used as an inhibitor of styrene polymerization、a photoinitiator、an ultraviolet curing agent、and an additive (plastics、cosmetics、coatings、and adhesives)、[HSDB] Occurs naturally in some foods、[AIHA] Benzophenone (BZP)、and substituted BZP numbered 1-12、trade mark Uvinul、are photo-screen agents widely used in sunscreens and in cosmetics、such as antiaging creams and hair sprays and shampoos、paints、and plastics. [Kanerva、p. 1755]、Painting (Pigments、Binders、and Biocides) [Category: Paint]、Working with Glues and Adhesives [Category: Other]、Plastic Composites Manufacturing [Category: Industry]、For benzophenone (USEPA、OPP Pesticide Code: 000315) 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.、Fixative for heavy perfumes、such as geranium、new-mown hay、especially when used in soaps. In the manufacture of antihistamines、hypnotics、insecticides.、Organic synthesis、... derivatives are used as ultraviolet absorbers、flavoring、... polymerization inhibitor for styrene、Paints、lacquers and varnish industry、intermediate.、For more Uses (Complete) data for BENZOPHENONE (7 total)、please visit the HSDB record page.、Benzophenone is found in fruits. Benzophenone is a widely used building block in organic chemistry、being the parent diarylketone.、Use Classification: Fragrance Ingredients、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Flavoring Agents -> JECFA Flavorings Index、Cosmetics -> Uv absorber、Industry Uses: Photosensitive agent、Surface modifier、Not Known or Reasonably Ascertainable、Anti-stain agent、Tanning agents not otherwise specified、Consumer Uses: Anti-stain agent、Photosensitive agent、Household Products: Cosmetics product ingredient: Benzophenone、Also known as: phenyl ketone、diphenyl ketone、benzoyl benzene、Source: Benzophenone is a synthetic compound that blocks ultraviolet (UV) light. The addition of benzophenone to products protects other ingredients from UV damage and prevents product degradation. Manufacturers often add compounds related to benzophenone such as benzophenone-2、benzophenone-3、and benzophenone-8 to sunscreens and other cosmetics to give them a Sun Protection Factor (SPF).、Potential health impacts: Benzophenone can enter the body by inhalation、through skin absorption、or by ingestion、depending on the specific product. Studies of rats that ingested benzophenone found increased rates of liver and kidney cancer. The International Agency for Research on Cancer (IARC) categorizes benzophenone as an animal carcinogen and a possible human carcinogen. Benzophenone and its metabolites mimic estrogen activity in mice. Researchers have found that derivatives of benzophenone、including benzophenone-2 and benzophenone-3 (oxybenzone)、are endocrine disruptors with the potential to interrupt the body's normal hormone function.、Product count: 269、Information on 42 consumer products that contain Benzophenone in the following categories is provided:、• Auto Products、• Commercial、Institutional、• Home Maintenance、• Inside the Home、• Personal Care、Methods of Manufacturing: Benzophenone is usually produced by atmospheric oxidation of diphenylmethane in the presence of metal catalysts such as copper naphthenate. Other processes include Friedel-Crafts acylation of benzene with benzoyl chloride or of benzene with phosgene.、Prepared by the Friedel-Crafts ketone synthesis from benzene and benzoyl chloride in the presence of AlCl3 ... By decarboxylation of o-benzoylbenzoic acid in the presence of copper catalyst.、Formulations、Preparations: Grade: Free from chlorine (FFC)、also FCC (food chemicals codex).、U.S. Production: 2023: 1、000、000 - <2、500、000 lb、2022: 2、000 - <4、2021: 2、2020: 2、This chemical is listed as a High Production Volume (HPV) (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).、Methanone、diphenyl- 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、Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Methanone、diphenyl-. Aggregated National Production Volume: 1 to < 10 million pounds.、Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone、diphenyl-. National Production Volume: 3、867、158 lb、yr.、General Manufacturing Information: Plastics Product Manufacturing、Paint and Coating Manufacturing、Plastics Material and Resin Manufacturing、Adhesive Manufacturing、Printing Ink Manufacturing、Asphalt Paving、Roofing、and Coating Materials Manufacturing、diphenyl-: ACTIVE、Purification: crystallization from alcohol.、Benzophenone-1、-3、-4、-5、-9 and-11 are compounds made from 2-hydroxybenzophenone. These compounds are powders. In cosmetics and personal care products、Benzophenone-1 and Benzophenone-3 are used mostly in the formulation of nail polishes and enamels. These Benzophenone ingredients are also used in bath products、makeup products、hair products、sunscreens and skin care products.、Benzophenones、Benzophenone can m
类别医药中间体

应用领域

登记用途:Uses: Used in perfumes、flavoring agents、and organic synthesis、Also used as an inhibitor of styrene polymerization、a photoinitiator、an ultraviolet curing agent、and an additive (plastics、cosmetics、coatings、and adhesives)、[HSDB] Occurs naturally in some foods、[AIHA] Benzophenone (BZP)、and substituted BZP numbered 1-12、trade mark Uvinul、are photo-screen agents widely used in sunscreens and in cosmetics、such as antiaging creams and hair sprays and shampoos、paints、and plastics. [Kanerva、p. 1755]、Painting (Pigments、Binders、and Biocides) [Category: Paint]、Working with Glues and Adhesives [Category: Other]、Plastic Composites Manufacturing [Category: Industry]、For benzophenone (USEPA、OPP Pesticide Code: 000315) 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.、Fixative for heavy perfumes、such as geranium、new-mown hay、especially when used in soaps. In the manufacture of antihistamines、hypnotics、insecticides.、Organic synthesis、... derivatives are used as ultraviolet absorbers、flavoring、... polymerization inhibitor for styrene、Paints、lacquers and varnish industry、intermediate.、For more Uses (Complete) data for BENZOPHENONE (7 total)、please visit the HSDB record page.、Benzophenone is found in fruits. Benzophenone is a widely used building block in organic chemistry、being the parent diarylketone.、Use Classification: Fragrance Ingredients、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Flavoring Agents -> JECFA Flavorings Index、Cosmetics -> Uv absorber、Industry Uses: Photosensitive agent、Surface modifier、Not Known or Reasonably Ascertainable、Anti-stain agent、Tanning agents not otherwise specified、Consumer Uses: Anti-stain agent、Photosensitive agent、Household Products: Cosmetics product ingredient: Benzophenone、Also known as: phenyl ketone、diphenyl ketone、benzoyl benzene、Source: Benzophenone is a synthetic compound that blocks ultraviolet (UV) light. The addition of benzophenone to products protects other ingredients from UV damage and prevents product degradation. Manufacturers often add compounds related to benzophenone such as benzophenone-2、benzophenone-3、and benzophenone-8 to sunscreens and other cosmetics to give them a Sun Protection Factor (SPF).、Potential health impacts: Benzophenone can enter the body by inhalation、through skin absorption、or by ingestion、depending on the specific product. Studies of rats that ingested benzophenone found increased rates of liver and kidney cancer. The International Agency for Research on Cancer (IARC) categorizes benzophenone as an animal carcinogen and a possible human carcinogen. Benzophenone and its metabolites mimic estrogen activity in mice. Researchers have found that derivatives of benzophenone、including benzophenone-2 and benzophenone-3 (oxybenzone)、are endocrine disruptors with the potential to interrupt the body's normal hormone function.、Product count: 269、Information on 42 consumer products that contain Benzophenone in the following categories is provided:、• Auto Products、• Commercial、Institutional、• Home Maintenance、• Inside the Home、• Personal Care、Methods of Manufacturing: Benzophenone is usually produced by atmospheric oxidation of diphenylmethane in the presence of metal catalysts such as copper naphthenate. Other processes include Friedel-Crafts acylation of benzene with benzoyl chloride or of benzene with phosgene.、Prepared by the Friedel-Crafts ketone synthesis from benzene and benzoyl chloride in the presence of AlCl3 ... By decarboxylation of o-benzoylbenzoic acid in the presence of copper catalyst.、Formulations、Preparations: Grade: Free from chlorine (FFC)、also FCC (food chemicals codex).、U.S. Production: 2023: 1、000、000 - <2、500、000 lb、2022: 2、000 - <4、2021: 2、2020: 2、This chemical is listed as a High Production Volume (HPV) (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).、Methanone、diphenyl- 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、Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Methanone、diphenyl-. Aggregated National Production Volume: 1 to < 10 million pounds.、Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone、diphenyl-. National Production Volume: 3、867、158 lb、yr.、General Manufacturing Information: Plastics Product Manufacturing、Paint and Coating Manufacturing、Plastics Material and Resin Manufacturing、Adhesive Manufacturing、Printing Ink Manufacturing、Asphalt Paving、Roofing、and Coating Materials Manufacturing、diphenyl-: ACTIVE、Purification: crystallization from alcohol.、Benzophenone-1、-3、-4、-5、-9 and-11 are compounds made from 2-hydroxybenzophenone. These compounds are powders. In cosmetics and personal care products、Benzophenone-1 and Benzophenone-3 are used mostly in the formulation of nail polishes and enamels. These Benzophenone ingredients are also used in bath products、makeup products、hair products、sunscreens and skin care products.、Benzophenones、Benzophenone can m。

技术档案

这个产品是什么

二苯甲酮 是一种化工化合物,登记 CAS 号为 119-61-9,分子式 C13H10O(分子量 182.22),归属于医药中间体大类化工原料。

识别信息

登记 CAS 号:119-61-9

其分子式 C13H10O 由 13 个碳、10 个氢、1 个氧 组成。

别名/同义词:二苯甲酮 · Benzophenone

所属分类:医药中间体

常见问题

二苯甲酮 的 CAS 号是多少?

二苯甲酮 的 CAS 登记号为 119-61-9。

二苯甲酮 的分子式与分子量是多少?

分子式 C13H10O,分子量 182.22。

二苯甲酮 还有哪些别名?

别名/同义词:二苯甲酮、Benzophenone。

二苯甲酮 的登记用途是什么?

登记用途:Uses: Used in perfumes、flavoring agents、and organic synthesis、Also used as an inhibitor of styrene polymerization、a photoinitiator、an ultraviolet curing agent、and an additive (plastics、cosmetics、coatings、and adhesives)、[HSDB] Occurs naturally in some foods、[AIHA] Benzophenone (BZP)、and substituted BZP numbered 1-12、trade mark Uvinul、are photo-screen agents widely used in sunscreens and in cosmetics、such as antiaging creams and hair sprays and shampoos、paints、and plastics. [Kanerva、p. 1755]、Painting (Pigments、Binders、and Biocides) [Category: Paint]、Working with Glues and Adhesives [Category: Other]、Plastic Composites Manufacturing [Category: Industry]、For benzophenone (USEPA、OPP Pesticide Code: 000315) 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.、Fixative for heavy perfumes、such as geranium、new-mown hay、especially when used in soaps. In the manufacture of antihistamines、hypnotics、insecticides.、Organic synthesis、... derivatives are used as ultraviolet absorbers、flavoring、... polymerization inhibitor for styrene、Paints、lacquers and varnish industry、intermediate.、For more Uses (Complete) data for BENZOPHENONE (7 total)、please visit the HSDB record page.、Benzophenone is found in fruits. Benzophenone is a widely used building block in organic chemistry、being the parent diarylketone.、Use Classification: Fragrance Ingredients、Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes、Flavoring Agents -> JECFA Flavorings Index、Cosmetics -> Uv absorber、Industry Uses: Photosensitive agent、Surface modifier、Not Known or Reasonably Ascertainable、Anti-stain agent、Tanning agents not otherwise specified、Consumer Uses: Anti-stain agent、Photosensitive agent、Household Products: Cosmetics product ingredient: Benzophenone、Also known as: phenyl ketone、diphenyl ketone、benzoyl benzene、Source: Benzophenone is a synthetic compound that blocks ultraviolet (UV) light. The addition of benzophenone to products protects other ingredients from UV damage and prevents product degradation. Manufacturers often add compounds related to benzophenone such as benzophenone-2、benzophenone-3、and benzophenone-8 to sunscreens and other cosmetics to give them a Sun Protection Factor (SPF).、Potential health impacts: Benzophenone can enter the body by inhalation、through skin absorption、or by ingestion、depending on the specific product. Studies of rats that ingested benzophenone found increased rates of liver and kidney cancer. The International Agency for Research on Cancer (IARC) categorizes benzophenone as an animal carcinogen and a possible human carcinogen. Benzophenone and its metabolites mimic estrogen activity in mice. Researchers have found that derivatives of benzophenone、including benzophenone-2 and benzophenone-3 (oxybenzone)、are endocrine disruptors with the potential to interrupt the body's normal hormone function.、Product count: 269、Information on 42 consumer products that contain Benzophenone in the following categories is provided:、• Auto Products、• Commercial、Institutional、• Home Maintenance、• Inside the Home、• Personal Care、Methods of Manufacturing: Benzophenone is usually produced by atmospheric oxidation of diphenylmethane in the presence of metal catalysts such as copper naphthenate. Other processes include Friedel-Crafts acylation of benzene with benzoyl chloride or of benzene with phosgene.、Prepared by the Friedel-Crafts ketone synthesis from benzene and benzoyl chloride in the presence of AlCl3 ... By decarboxylation of o-benzoylbenzoic acid in the presence of copper catalyst.、Formulations、Preparations: Grade: Free from chlorine (FFC)、also FCC (food chemicals codex).、U.S. Production: 2023: 1、000、000 - <2、500、000 lb、2022: 2、000 - <4、2021: 2、2020: 2、This chemical is listed as a High Production Volume (HPV) (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).、Methanone、diphenyl- 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、Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Methanone、diphenyl-. Aggregated National Production Volume: 1 to < 10 million pounds.、Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone、diphenyl-. National Production Volume: 3、867、158 lb、yr.、General Manufacturing Information: Plastics Product Manufacturing、Paint and Coating Manufacturing、Plastics Material and Resin Manufacturing、Adhesive Manufacturing、Printing Ink Manufacturing、Asphalt Paving、Roofing、and Coating Materials Manufacturing、diphenyl-: ACTIVE、Purification: crystallization from alcohol.、Benzophenone-1、-3、-4、-5、-9 and-11 are compounds made from 2-hydroxybenzophenone. These compounds are powders. In cosmetics and personal care products、Benzophenone-1 and Benzophenone-3 are used mostly in the formulation of nail polishes and enamels. These Benzophenone ingredients are also used in bath products、makeup products、hair products、sunscreens and skin care products.、Benzophenones、Benzophenone can m。

二苯甲酮 属于哪个分类?

所属分类:医药中间体。

PubChem 公开数据

二苯甲酮(CAS 119-61-9)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119-61-9
PubChem CID3102
分子式C13H10O
分子量182.07 g/mol
IUPAC 名称diphenylmethanone
InChIKeyRWCCWEUUXYIKHB-UHFFFAOYSA-N
UNII(FDA)701M4TTV9O
ChEBI 编号CHEBI:41308
FEMA 编号2134
JECFA 编号831

计算分子描述符

Molecular Weight182.22
XLogP33.4
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass182.073164938
Monoisotopic Mass182.073164938
Topological Polar Surface Area17.1
Heavy Atom Count14

在册的理化数值

Boiling Point582.6 °F at 760 mmHg (NTP, 1992)
Boiling Point305.4
Boiling Point305.9 °C
Boiling Point305.00 to 307.00 °C. @ 760.00 mm Hg
Boiling Point305 °C
Boiling Point583 °F
Boiling Point305.4 °C @760 [mm Hg]
Melting Point47.8
Melting Point48.5 °C
Melting Point26 °C

同义词与商品名

BENZOPHENONE; 119-61-9; diphenylmethanone; Diphenyl ketone; Benzoylbenzene; Methanone, diphenyl-; Phenyl ketone; alpha-Oxoditane; Ketone, diphenyl; Diphenylketone; Benzene, benzoyl-; alpha-Oxodiphenylmethane; Kayacure bp; DTXSID0021961; Adjutan 6016; Caswell No. 081G

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
Floral
No safety concern at current levels of intake when used as a flavouring agent
GHS 通报统计1.8% (84 / 4790)

GHS 危害分类

GHS 通报统计1.8% (84 / 4790)
已通报的危害声明H350, H373 (37.4%), H411 (74.8%), H302, H320, H351, H401, H400

公开数据库对它的描述

二苯甲酮 的 CAS 号为 119-61-9,分子式 C13H10O,分子量 182.07 g/mol。 UNII 701M4TTV9O; ChEBI 41308; InChIKey RWCCWEUUXYIKHB-UHFFFAOYSA-N. Boiling Point: 582.6 °F at 760 mmHg (NTP, 1992); Boiling Point: 305.4; Boiling Point: 305.9 °C.

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

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