DL-1-Phenylethanol (CAS 13323-81-4) — formula C8H10O, molecular weight 122.16; category organic chemicals.
| CAS Number | 13323-81-4 |
|---|---|
| Molecular Formula | C8H10O |
| Molecular Weight | 122.16 |
| Melting Point | 68 °F (NTP, 1992) |
| Boiling Point | 399 °F at 745 mmHg (NTP, 1992) |
| LogP | 1.4 |
| Applications | Uses: Used in perfumery, as a flavoring agent, in dyes, as a laboratory reagent, in stoving enamels, in cellulose nitrate and acetyl cellulose lacquers, as an additive in paint-removal agents, [HSDB] Used as an un-isolated intermediate in styrene production, as an antimicrobial agent, [CHEMINFO], Painting (Solvents) [Category: Paint], Painting (Pigments, Binders, and Biocides) [Category: Paint], PERFUMERY, FLAVORING, DYES, LABORATORY REAGENT, Methylbenzyl alcohol can be used like benzyl alcohol, and can be employed in stoving enamels. In cellulose nitrate and acetyl cellulose lacquers, methylbenzyl alcohol helps to improve flow and film formation and prevents blushing at relatively high atmospheric humidity levels. It has also proved to be a useful additive in paint-removal agents on account of its dissolution properties and long evaporation time., Use Classification: Fragrance Ingredients, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Intermediate, Processing aids not otherwise specified, Methods of Manufacturing: REDUCTION OF ACETOPHENONE, REACTION OF METHYL MAGNESIUM CHLORIDE AND BENZALDEHYDE, OXIDATION OF ETHYLBENZENE, In the hydroperoxide process, an organic hydroperoxide is used to epoxidize propylene, an organic alcohol is a coproduct., Formulations, Preparations: GRADE: FCC, U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 1, 2021: 1, 2020: 1, (1974) 4.54X10+6 G (CONSUMPTION AS FRAGRANCE), (1977) LESS THAN 2.7X10+11 G-UNISOLATED INT, U.S. Imports: (1977) 1.05X10+8 GRAMS (PRINCPL CUSTMS DISTS), (1979) 6.81X10+7 GRAMS (PRINCPL CUSTMS DISTS), General Manufacturing Information: Petrochemical Manufacturing, Benzenemethanol, .alpha.-methyl-: ACTIVE, TWO OPTICALLY ACTIVE ISOMERS EXIST. COMMERCIAL PRODUCT IS RACEMIC FORM., REPORTED USES: NON-ALCOHOLIC BEVERAGES 4.6 PPM, ICE CREAM, ICES, ETC 3.8 PPM, CANDY 6.8 PPM, BAKED GOODS 9.0 PPM, GELATINS & PUDDINGS 4.0 PPM, CHEWING GUM 0.30 PPM. |
| Category | Organic Chemicals |
Documented applications: Uses: Used in perfumery, as a flavoring agent, in dyes, as a laboratory reagent, in stoving enamels, in cellulose nitrate and acetyl cellulose lacquers, as an additive in paint-removal agents, [HSDB] Used as an un-isolated intermediate in styrene production, as an antimicrobial agent, [CHEMINFO], Painting (Solvents) [Category: Paint], Painting (Pigments, Binders, and Biocides) [Category: Paint], PERFUMERY, FLAVORING, DYES, LABORATORY REAGENT, Methylbenzyl alcohol can be used like benzyl alcohol, and can be employed in stoving enamels. In cellulose nitrate and acetyl cellulose lacquers, methylbenzyl alcohol helps to improve flow and film formation and prevents blushing at relatively high atmospheric humidity levels. It has also proved to be a useful additive in paint-removal agents on account of its dissolution properties and long evaporation time., Use Classification: Fragrance Ingredients, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Intermediate, Processing aids not otherwise specified, Methods of Manufacturing: REDUCTION OF ACETOPHENONE, REACTION OF METHYL MAGNESIUM CHLORIDE AND BENZALDEHYDE, OXIDATION OF ETHYLBENZENE, In the hydroperoxide process, an organic hydroperoxide is used to epoxidize propylene, an organic alcohol is a coproduct., Formulations, Preparations: GRADE: FCC, U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 1, 2021: 1, 2020: 1, (1974) 4.54X10+6 G (CONSUMPTION AS FRAGRANCE), (1977) LESS THAN 2.7X10+11 G-UNISOLATED INT, U.S. Imports: (1977) 1.05X10+8 GRAMS (PRINCPL CUSTMS DISTS), (1979) 6.81X10+7 GRAMS (PRINCPL CUSTMS DISTS), General Manufacturing Information: Petrochemical Manufacturing, Benzenemethanol, .alpha.-methyl-: ACTIVE, TWO OPTICALLY ACTIVE ISOMERS EXIST. COMMERCIAL PRODUCT IS RACEMIC FORM., REPORTED USES: NON-ALCOHOLIC BEVERAGES 4.6 PPM, ICE CREAM, ICES, ETC 3.8 PPM, CANDY 6.8 PPM, BAKED GOODS 9.0 PPM, GELATINS & PUDDINGS 4.0 PPM, CHEWING GUM 0.30 PPM..
DL-1-Phenylethanol is a carbon-based organic compound with CAS registry number 13323-81-4 and molecular formula C8H10O (molecular weight 122.16), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 13323-81-4
Its molecular formula C8H10O comprises 8 C, 10 H, 1 O atoms.
Also known as: DL-1-Phenylethanol · DL-1-苯乙醇
Category: organic chemicals
The CAS registry number of DL-1-Phenylethanol is 13323-81-4.
Molecular formula C8H10O, molecular weight 122.16.
It is also registered under: DL-1-Phenylethanol, DL-1-苯乙醇.
Recorded applications: Uses: Used in perfumery, as a flavoring agent, in dyes, as a laboratory reagent, in stoving enamels, in cellulose nitrate and acetyl cellulose lacquers, as an additive in paint-removal agents, [HSDB] Used as an un-isolated intermediate in styrene production, as an antimicrobial agent, [CHEMINFO], Painting (Solvents) [Category: Paint], Painting (Pigments, Binders, and Biocides) [Category: Paint], PERFUMERY, FLAVORING, DYES, LABORATORY REAGENT, Methylbenzyl alcohol can be used like benzyl alcohol, and can be employed in stoving enamels. In cellulose nitrate and acetyl cellulose lacquers, methylbenzyl alcohol helps to improve flow and film formation and prevents blushing at relatively high atmospheric humidity levels. It has also proved to be a useful additive in paint-removal agents on account of its dissolution properties and long evaporation time., Use Classification: Fragrance Ingredients, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Intermediate, Processing aids not otherwise specified, Methods of Manufacturing: REDUCTION OF ACETOPHENONE, REACTION OF METHYL MAGNESIUM CHLORIDE AND BENZALDEHYDE, OXIDATION OF ETHYLBENZENE, In the hydroperoxide process, an organic hydroperoxide is used to epoxidize propylene, an organic alcohol is a coproduct., Formulations, Preparations: GRADE: FCC, U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 1, 2021: 1, 2020: 1, (1974) 4.54X10+6 G (CONSUMPTION AS FRAGRANCE), (1977) LESS THAN 2.7X10+11 G-UNISOLATED INT, U.S. Imports: (1977) 1.05X10+8 GRAMS (PRINCPL CUSTMS DISTS), (1979) 6.81X10+7 GRAMS (PRINCPL CUSTMS DISTS), General Manufacturing Information: Petrochemical Manufacturing, Benzenemethanol, .alpha.-methyl-: ACTIVE, TWO OPTICALLY ACTIVE ISOMERS EXIST. COMMERCIAL PRODUCT IS RACEMIC FORM., REPORTED USES: NON-ALCOHOLIC BEVERAGES 4.6 PPM, ICE CREAM, ICES, ETC 3.8 PPM, CANDY 6.8 PPM, BAKED GOODS 9.0 PPM, GELATINS & PUDDINGS 4.0 PPM, CHEWING GUM 0.30 PPM..
Category: Organic Chemicals.
Independent reference data for DL-1-Phenylethanol (CAS 13323-81-4), compiled from public chemistry databases.
| CAS Registry Number | 13323-81-4 |
|---|---|
| PubChem CID | 7409 |
| Molecular formula | C8H10O |
| IUPAC name | 1-phenylethanol |
| UNII (FDA) | E6O895DQ52 |
| FEMA number | 2685 |
| JECFA number | 799 |
| Molecular Weight | 122.16 |
|---|---|
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 122.073164938 |
| Monoisotopic Mass | 122.073164938 |
| Topological Polar Surface Area | 20.2 |
| Heavy Atom Count | 9 |
| Boiling Point | 399 °F at 745 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | 204 °C |
| Boiling Point | 204.00 to 205.00 °C. @ 745.00 mm Hg |
| Melting Point | 68 °F (NTP, 1992) |
| Melting Point | 20.7 °C |
| Melting Point | 20 °C |
| Flash Point | 185 °F (NTP, 1992) |
| Flash Point | 93 °C |
| Flash Point | 200 °F (93 °C) (CLOSED CUP) |
| Solubility | In water, 1,950 mg/l @ 25 °C |
1-Phenylethanol; 98-85-1; ALPHA-METHYLBENZYL ALCOHOL; Styrallyl alcohol; Methylphenyl carbinol; Styralyl alcohol; Methylphenylcarbinol; 1-Phenethyl alcohol; (1-Hydroxyethyl)benzene; 1-Phenylethyl alcohol; Phenylmethylcarbinol; alpha-Methylbenzenemethanol; alpha-Phenylethanol; alpha-Phenylethyl alcohol; 1-Phenyl-1-hydroxyethane; Ethanol, 1-phenyl-
| Regulatory & Food Contact | EU Flavoring substances FDA Substance added to food: FLAVORING AGENT OR ADJUVANT Flavoring Agents FLAVOURING_AGENT: Flavouring Agent Floral, Honey, Rose JECFA ADI: 0-0.1 mg/kg bw (1993) |
|---|---|
| GHS notification summary | 1.9% (37 / 1934) |
| GHS notification summary | 1.9% (37 / 1934) |
|---|---|
| Reported hazard statements | H302 (98.1%), H319 (77.2%), H315 (100%), H318 (100%), H335 (100%) |
This chemical does not meet GHS hazard criteria for 1.9% (37 of 1934) of reports.
H302 (98.1%): Harmful if swallowed [Warning Acute toxicity, oral]
DL-1-Phenylethanol · CAS 13323-81-4 · C8H10O. UNII E6O895DQ52. Boiling Point: 399 °F at 745 mmHg (NTP, 1992); Boiling Point: 204 °C; Boiling Point: 204.00 to 205.00 °C. @ 745.00 mm Hg.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: DL-1-苯乙醇