[1,1-Biphenyl]-2-yloxy(9CI) (CAS 73829-47-7) — formula C12H10O, molecular weight 170.21; category organic chemicals.
| CAS Number | 73829-47-7 |
|---|---|
| Molecular Formula | C12H10O |
| Molecular Weight | 170.21 |
| Melting Point | 131.9 to 135.5 °F (NTP, 1992) |
| Boiling Point | 527 °F at 760 mmHg (NTP, 1992) |
| LogP | 3.1 |
| Applications | Uses: Used as a dye intermediate, germicide, fungicide, disinfectant, and plasticizer, to manufacture rubber chemicals, in food packaging, as a preservative in water-oil emulsions, antimicrobial preservative in cosmetics, [HSDB] Used as an antimicrobial additive in the manufacture of metalworking fluids, leather, adhesives, and textiles, [Merck Index], Metal Machining [Category: Heat or Machine], Textiles (Fiber & Fabric Manufacturing) [Category: Industry], Working with Glues and Adhesives [Category: Other], Using Disinfectants or Biocides [Category: Clean], Leather Tanning and Processing [Category: Industry], For 2-phenylphenol (USEPA, OPP Pesticide Code: 064103) ACTIVE products with label matches., SRP: Registered for 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., Used in products predominantly as a disinfectant, antimicrobial, preservative, antioxidant, and sanitizing agent in various industries., Wood preserving ... used for sapstain control in freshly cut lumber, Fungicide for citrus (postharvest use), disinfectant (eg, for cutting oils, timber, + paper), dyestuff carrier for polyester fibers, For more Uses (Complete) data for o-Phenylphenol (16 total), please visit the HSDB record page., Use (kg, approx.) in Germany (2009): >250, Consumption (g per capita, approx.) in Germany (2009): 0.00305, Calculated removal (%): 82.5, 2-Biphenylol is found in lemon. It is an antifungal agent and preservative. 2-Biphenylol is used for post-harvest control of storage disease in apples, citrus fruit, stone fruit, tomatoes, cucumber and peppers through the use of impregnated wrapping materials or by direct application in a wax. 2-Biphenylol is used in food seasonings. The practical way of treatment is to immerse citrus fruit in an alkaline aqueous solution of the parent compound or its Na salt., Use Classification: Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Fungicides, Cosmetics -> Preservative, Household Products: Cosmetics product ingredient: o-Phenylphenol, Source: o-Phenylphenol is used to control the growth of fungus on produce. It is also used as an industrial disinfectant. It is an ingredient in some cleansers marketed for sensitive skin., Potential health impacts: People are mainly exposed to o-phenylphenol by ingestion, inhalation, or by skin contact. o-Phenylphenol is irritating to the skin, eyes, nose, and throat. Animal studies have shown that o-phenylphenol can damage the liver and kidneys. The International Agency for Research on Cancer (IARC) considers o-phenylphenol an animal carcinogen. The U.S. Environmental Protection Agency and California Proposition 65 list o-phenylphenol as a human carcinogen., Product count: 8, Information on 25 consumer products that contain o-Phenylphenol in the following categories is provided:, • Commercial, Institutional, • Inside the Home, • Personal Care, • Pesticides, Methods of Manufacturing: By hydrogenation of 2-cyclohexylidenecyclohexanone produced by the base catalyzed dimerization of cyclohexanone., Either synthesized directly or isolated as a byproduct in the production of phenol by the hydrolysis of monochlorobenzene., Prepared from phenyl ether., Biphenyl (sulphonation, alkali fusion, coproduced with p-phenylphenol). Chlorobenzene (arylation, base-catalyzed hydrolysis, coproduced with p-phenylphenol). Xylenol, mixed (fractionation, alkali extraction, coproduced with biphenyl), For more Methods of Manufacturing (Complete) data for o-Phenylphenol (7 total), Formulations, Preparations: Coldcide 0.25%: Active Ingredients 0.2750% Glutaral, 0.0027% 4-tert-Amylphenol, 0.0137% o-Phenylphenol, Staphene Disinfectant Spray And Deodorizer: Active Ingredients 53.096% Ethyl alcohol, 0.077% 2-Benzyl-4-chlorophenol, 0.074% 4-tert-Amylphenol, 0.041% o-Phenylphenol, 0.042% Alkyl* dimethyl benzyl ammonium chloride *(60%C14, 30%C16, 5%C1 8, 5%C12), 0.042% Alkyl* dimethyl ethylbenzyl ammonium chloride *(50%C12, 30%C14, 17%C16, 3%C18), Easy-Dab Bacteriostatic Creme Cleanser: Active Ingredient 0.05% o-Phenylphenol, Steriphene II Brand Disinfectant Deodorant: Active Ingredients 64.000% Ethyl alcohol, 0.071% 2-Benzyl-4-chlorophenol, 0.051% o-Phenylphenol, For more Formulations, Preparations (Complete) data for o-Phenylphenol (92 total), U.S. Production: (1976) Probably greater than 4.54x10+5 g, (1978) Probably greater than 4.54x10+5 g, Current global production is estimated to be less than 10 million pounds per year., [1, 1'-Biphenyl]-2-ol 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).[EPA, Office of Pollution Prevention and Toxics, High Production Volume (HPV) Challenge Program., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3538], [US EPA, Non-confidential Production Volume Information Submitted by Companies for Chemicals Under the 1986-2002 Inventory Update Rule (IUR)., U.S. Imports: (1976) 6.01X10+6 g (Princpl custms dists), (1978) 3.00X10+7 g (Princpl custms dists), General Manufacturing Information: [1, 1'-Biphenyl]-2-ol: ACTIVE, The tendency, of o-phenylphenol, to scald citrus fruits is reduced by addition of hexamine., Water sol sodium salt of o-phenylphenol is used for protecting water extendable paints against decomposition prior to use and is e |
| Category | Organic Chemicals |
Documented applications: Uses: Used as a dye intermediate, germicide, fungicide, disinfectant, and plasticizer, to manufacture rubber chemicals, in food packaging, as a preservative in water-oil emulsions, antimicrobial preservative in cosmetics, [HSDB] Used as an antimicrobial additive in the manufacture of metalworking fluids, leather, adhesives, and textiles, [Merck Index], Metal Machining [Category: Heat or Machine], Textiles (Fiber & Fabric Manufacturing) [Category: Industry], Working with Glues and Adhesives [Category: Other], Using Disinfectants or Biocides [Category: Clean], Leather Tanning and Processing [Category: Industry], For 2-phenylphenol (USEPA, OPP Pesticide Code: 064103) ACTIVE products with label matches., SRP: Registered for 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., Used in products predominantly as a disinfectant, antimicrobial, preservative, antioxidant, and sanitizing agent in various industries., Wood preserving ... used for sapstain control in freshly cut lumber, Fungicide for citrus (postharvest use), disinfectant (eg, for cutting oils, timber, + paper), dyestuff carrier for polyester fibers, For more Uses (Complete) data for o-Phenylphenol (16 total), please visit the HSDB record page., Use (kg, approx.) in Germany (2009): >250, Consumption (g per capita, approx.) in Germany (2009): 0.00305, Calculated removal (%): 82.5, 2-Biphenylol is found in lemon. It is an antifungal agent and preservative. 2-Biphenylol is used for post-harvest control of storage disease in apples, citrus fruit, stone fruit, tomatoes, cucumber and peppers through the use of impregnated wrapping materials or by direct application in a wax. 2-Biphenylol is used in food seasonings. The practical way of treatment is to immerse citrus fruit in an alkaline aqueous solution of the parent compound or its Na salt., Use Classification: Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Fungicides, Cosmetics -> Preservative, Household Products: Cosmetics product ingredient: o-Phenylphenol, Source: o-Phenylphenol is used to control the growth of fungus on produce. It is also used as an industrial disinfectant. It is an ingredient in some cleansers marketed for sensitive skin., Potential health impacts: People are mainly exposed to o-phenylphenol by ingestion, inhalation, or by skin contact. o-Phenylphenol is irritating to the skin, eyes, nose, and throat. Animal studies have shown that o-phenylphenol can damage the liver and kidneys. The International Agency for Research on Cancer (IARC) considers o-phenylphenol an animal carcinogen. The U.S. Environmental Protection Agency and California Proposition 65 list o-phenylphenol as a human carcinogen., Product count: 8, Information on 25 consumer products that contain o-Phenylphenol in the following categories is provided:, • Commercial, Institutional, • Inside the Home, • Personal Care, • Pesticides, Methods of Manufacturing: By hydrogenation of 2-cyclohexylidenecyclohexanone produced by the base catalyzed dimerization of cyclohexanone., Either synthesized directly or isolated as a byproduct in the production of phenol by the hydrolysis of monochlorobenzene., Prepared from phenyl ether., Biphenyl (sulphonation, alkali fusion, coproduced with p-phenylphenol). Chlorobenzene (arylation, base-catalyzed hydrolysis, coproduced with p-phenylphenol). Xylenol, mixed (fractionation, alkali extraction, coproduced with biphenyl), For more Methods of Manufacturing (Complete) data for o-Phenylphenol (7 total), Formulations, Preparations: Coldcide 0.25%: Active Ingredients 0.2750% Glutaral, 0.0027% 4-tert-Amylphenol, 0.0137% o-Phenylphenol, Staphene Disinfectant Spray And Deodorizer: Active Ingredients 53.096% Ethyl alcohol, 0.077% 2-Benzyl-4-chlorophenol, 0.074% 4-tert-Amylphenol, 0.041% o-Phenylphenol, 0.042% Alkyl* dimethyl benzyl ammonium chloride *(60%C14, 30%C16, 5%C1 8, 5%C12), 0.042% Alkyl* dimethyl ethylbenzyl ammonium chloride *(50%C12, 30%C14, 17%C16, 3%C18), Easy-Dab Bacteriostatic Creme Cleanser: Active Ingredient 0.05% o-Phenylphenol, Steriphene II Brand Disinfectant Deodorant: Active Ingredients 64.000% Ethyl alcohol, 0.071% 2-Benzyl-4-chlorophenol, 0.051% o-Phenylphenol, For more Formulations, Preparations (Complete) data for o-Phenylphenol (92 total), U.S. Production: (1976) Probably greater than 4.54x10+5 g, (1978) Probably greater than 4.54x10+5 g, Current global production is estimated to be less than 10 million pounds per year., [1, 1'-Biphenyl]-2-ol 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).[EPA, Office of Pollution Prevention and Toxics, High Production Volume (HPV) Challenge Program., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3538], [US EPA, Non-confidential Production Volume Information Submitted by Companies for Chemicals Under the 1986-2002 Inventory Update Rule (IUR)., U.S. Imports: (1976) 6.01X10+6 g (Princpl custms dists), (1978) 3.00X10+7 g (Princpl custms dists), General Manufacturing Information: [1, 1'-Biphenyl]-2-ol: ACTIVE, The tendency, of o-phenylphenol, to scald citrus fruits is reduced by addition of hexamine., Water sol sodium salt of o-phenylphenol is used for protecting water extendable paints against decomposition prior to use and is e.
[1,1-Biphenyl]-2-yloxy(9CI) is a carbon-based organic compound with CAS registry number 73829-47-7 and molecular formula C12H10O (molecular weight 170.21), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 73829-47-7
Its molecular formula C12H10O comprises 12 C, 10 H, 1 O atoms.
Also known as: [1,1-Biphenyl]-2-yloxy(9CI) · [1,1-联苯]-2-基氧基(9Cl)
Category: organic chemicals
The CAS registry number of [1,1-Biphenyl]-2-yloxy(9CI) is 73829-47-7.
Molecular formula C12H10O, molecular weight 170.21.
It is also registered under: [1,1-Biphenyl]-2-yloxy(9CI), [1,1-联苯]-2-基氧基(9Cl).
Recorded applications: Uses: Used as a dye intermediate, germicide, fungicide, disinfectant, and plasticizer, to manufacture rubber chemicals, in food packaging, as a preservative in water-oil emulsions, antimicrobial preservative in cosmetics, [HSDB] Used as an antimicrobial additive in the manufacture of metalworking fluids, leather, adhesives, and textiles, [Merck Index], Metal Machining [Category: Heat or Machine], Textiles (Fiber & Fabric Manufacturing) [Category: Industry], Working with Glues and Adhesives [Category: Other], Using Disinfectants or Biocides [Category: Clean], Leather Tanning and Processing [Category: Industry], For 2-phenylphenol (USEPA, OPP Pesticide Code: 064103) ACTIVE products with label matches., SRP: Registered for 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., Used in products predominantly as a disinfectant, antimicrobial, preservative, antioxidant, and sanitizing agent in various industries., Wood preserving ... used for sapstain control in freshly cut lumber, Fungicide for citrus (postharvest use), disinfectant (eg, for cutting oils, timber, + paper), dyestuff carrier for polyester fibers, For more Uses (Complete) data for o-Phenylphenol (16 total), please visit the HSDB record page., Use (kg, approx.) in Germany (2009): >250, Consumption (g per capita, approx.) in Germany (2009): 0.00305, Calculated removal (%): 82.5, 2-Biphenylol is found in lemon. It is an antifungal agent and preservative. 2-Biphenylol is used for post-harvest control of storage disease in apples, citrus fruit, stone fruit, tomatoes, cucumber and peppers through the use of impregnated wrapping materials or by direct application in a wax. 2-Biphenylol is used in food seasonings. The practical way of treatment is to immerse citrus fruit in an alkaline aqueous solution of the parent compound or its Na salt., Use Classification: Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Food Additives -> PRESERVATIVE -> JECFA Functional Classes, Fungicides, Cosmetics -> Preservative, Household Products: Cosmetics product ingredient: o-Phenylphenol, Source: o-Phenylphenol is used to control the growth of fungus on produce. It is also used as an industrial disinfectant. It is an ingredient in some cleansers marketed for sensitive skin., Potential health impacts: People are mainly exposed to o-phenylphenol by ingestion, inhalation, or by skin contact. o-Phenylphenol is irritating to the skin, eyes, nose, and throat. Animal studies have shown that o-phenylphenol can damage the liver and kidneys. The International Agency for Research on Cancer (IARC) considers o-phenylphenol an animal carcinogen. The U.S. Environmental Protection Agency and California Proposition 65 list o-phenylphenol as a human carcinogen., Product count: 8, Information on 25 consumer products that contain o-Phenylphenol in the following categories is provided:, • Commercial, Institutional, • Inside the Home, • Personal Care, • Pesticides, Methods of Manufacturing: By hydrogenation of 2-cyclohexylidenecyclohexanone produced by the base catalyzed dimerization of cyclohexanone., Either synthesized directly or isolated as a byproduct in the production of phenol by the hydrolysis of monochlorobenzene., Prepared from phenyl ether., Biphenyl (sulphonation, alkali fusion, coproduced with p-phenylphenol). Chlorobenzene (arylation, base-catalyzed hydrolysis, coproduced with p-phenylphenol). Xylenol, mixed (fractionation, alkali extraction, coproduced with biphenyl), For more Methods of Manufacturing (Complete) data for o-Phenylphenol (7 total), Formulations, Preparations: Coldcide 0.25%: Active Ingredients 0.2750% Glutaral, 0.0027% 4-tert-Amylphenol, 0.0137% o-Phenylphenol, Staphene Disinfectant Spray And Deodorizer: Active Ingredients 53.096% Ethyl alcohol, 0.077% 2-Benzyl-4-chlorophenol, 0.074% 4-tert-Amylphenol, 0.041% o-Phenylphenol, 0.042% Alkyl* dimethyl benzyl ammonium chloride *(60%C14, 30%C16, 5%C1 8, 5%C12), 0.042% Alkyl* dimethyl ethylbenzyl ammonium chloride *(50%C12, 30%C14, 17%C16, 3%C18), Easy-Dab Bacteriostatic Creme Cleanser: Active Ingredient 0.05% o-Phenylphenol, Steriphene II Brand Disinfectant Deodorant: Active Ingredients 64.000% Ethyl alcohol, 0.071% 2-Benzyl-4-chlorophenol, 0.051% o-Phenylphenol, For more Formulations, Preparations (Complete) data for o-Phenylphenol (92 total), U.S. Production: (1976) Probably greater than 4.54x10+5 g, (1978) Probably greater than 4.54x10+5 g, Current global production is estimated to be less than 10 million pounds per year., [1, 1'-Biphenyl]-2-ol 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).[EPA, Office of Pollution Prevention and Toxics, High Production Volume (HPV) Challenge Program., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3538], [US EPA, Non-confidential Production Volume Information Submitted by Companies for Chemicals Under the 1986-2002 Inventory Update Rule (IUR)., U.S. Imports: (1976) 6.01X10+6 g (Princpl custms dists), (1978) 3.00X10+7 g (Princpl custms dists), General Manufacturing Information: [1, 1'-Biphenyl]-2-ol: ACTIVE, The tendency, of o-phenylphenol, to scald citrus fruits is reduced by addition of hexamine., Water sol sodium salt of o-phenylphenol is used for protecting water extendable paints against decomposition prior to use and is e.
Category: Organic Chemicals.
Independent reference data for [1,1-Biphenyl]-2-yloxy(9CI) (CAS 73829-47-7), compiled from public chemistry databases.
| CAS 号 | 73829-47-7 |
|---|---|
| PubChem CID | 7017 |
| 分子式 | C12H10O |
| IUPAC 名称 | 2-phenylphenol |
| UNII（FDA） | D343Z75HT8 |
| FEMA 编号 | 3959 |
| JECFA 编号 | 735 |
| Molecular Weight | 170.21 |
|---|---|
| XLogP3 | 3.1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 170.073164938 |
| Monoisotopic Mass | 170.073164938 |
| Topological Polar Surface Area | 20.2 |
| Heavy Atom Count | 13 |
| Boiling Point | 527 °F at 760 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | 286 °C |
| Boiling Point | 282.00 to 285.00 °C. @ 760.00 mm Hg |
| Boiling Point | 282 °C |
| Boiling Point | 286 °C @760 [mm Hg] |
| Melting Point | 131.9 to 135.5 °F (NTP, 1992) |
| Melting Point | 59 °C |
| Melting Point | 56 °C |
| Melting Point | 58-60 °C |
| Melting Point | 57.5 °C |
2-Phenylphenol; 2-Hydroxybiphenyl; 90-43-7; O-PHENYLPHENOL; Biphenyl-2-ol; 2-Biphenylol; o-Hydroxybiphenyl; o-Hydroxydiphenyl; 2-Hydroxydiphenyl; o-Phenyl phenol; Orthoxenol; [1,1'-Biphenyl]-2-ol; Orthophenylphenol; Dowicide 1; o-Diphenylol; Torsite
| 法规与食品接触 | FDA Substance added to food: ANTIMICROBIAL AGENT, SURFACE-ACTIVE AGENT FDA Cumulative Estimated Daily Intake (CEDI): FCS FDA 21 CFR 中列出的食品接触物质清单：FCS PRESERVATIVE: Food Additives Flavoring Agents JECFA ADI: 0-0.4 mg/kg bw (1999) |
|---|
| 已通报的危害声明 | H314, H317, H318, H351, H400, H410, H315 (100%), H319 (97.3%) |
|---|
[1,1-联苯]-2-基氧基(9Cl) · CAS 73829-47-7 · C12H10O. UNII D343Z75HT8. Boiling Point: 527 °F at 760 mmHg (NTP, 1992); Boiling Point: 286 °C; Boiling Point: 282.00 to 285.00 °C. @ 760.00 mm Hg.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: [1,1-联苯]-2-基氧基(9Cl)