TRIS(DODECYLTHIO)ANTIMONY (CAS 6939-83-9) — formula C12H26S, molecular weight 202.40; category organic chemicals.
| CAS Number | 6939-83-9 |
|---|---|
| Molecular Formula | C12H26S |
| Molecular Weight | 202.40 |
| Melting Point | 19 °F (NTP, 1992) |
| Boiling Point | 511 to 541 °F at 760 mmHg (NTP, 1992) |
| LogP | 6.1 |
| Applications | Uses: Used in the production of drugs, insecticides, detergents, and synthetic rubber and as a flotation agent for metal refining, [ACGIH], Metal Extraction and Refining [Category: Industry], Polymerization regulator for styrene-butadiene rubber, In chemical syntheses of bactericides, as complexing agent, such as for the removal of metals from wastes, In manufacture of synthetic rubber, plastics, pharmaceuticals, fungicides, nonionic detergent, Flotation reagent, Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Flame retardant, Intermediate, Chain transfer agent, Lubricating agent, Antioxidant, Consumer Uses: Antioxidant, Methods of Manufacturing: Reaction of metallic hydrosulfide with n-dodecyl chloride, This mercaptan can be produced by action of hydrogen sulfide on lauryl alcohol or on dodecene., Formulations, Preparations: The commercial product is a mixture of isomers., Grade: 95%, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 10, 000 - <25, 2021: 10, 2020: 10, 1-Dodecanethiol 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)., (1972) Greater than 4.54X10+5 grams, (1975) Probably greater than 1.36X10+6 grams, General Manufacturing Information: Rubber Product Manufacturing, Petroleum Lubricating Oil and Grease Manufacturing, Plastics Product Manufacturing, Synthetic Rubber Manufacturing, Plastics Material and Resin Manufacturing, Construction, All Other Chemical Product and Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, 1-Dodecanethiol: ACTIVE, Thiols can be prepared by a variety of methods. The most-utilized of these synthetic methods for tertiary and secondary thiols is acid-catalyzed synthesis, for normal and secondary thiols, the most-utilized methods are free-radical-initiated, alcohol substitution, or halide substitution, for mercaptoalcohols, the most-utilized method is oxirane addition, and for mercaptoacids and mercaptonitriles, the most-utilized methods are Michael-type additions., Thiols |
| Category | Organic Chemicals |
Documented applications: Uses: Used in the production of drugs, insecticides, detergents, and synthetic rubber and as a flotation agent for metal refining, [ACGIH], Metal Extraction and Refining [Category: Industry], Polymerization regulator for styrene-butadiene rubber, In chemical syntheses of bactericides, as complexing agent, such as for the removal of metals from wastes, In manufacture of synthetic rubber, plastics, pharmaceuticals, fungicides, nonionic detergent, Flotation reagent, Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Flame retardant, Intermediate, Chain transfer agent, Lubricating agent, Antioxidant, Consumer Uses: Antioxidant, Methods of Manufacturing: Reaction of metallic hydrosulfide with n-dodecyl chloride, This mercaptan can be produced by action of hydrogen sulfide on lauryl alcohol or on dodecene., Formulations, Preparations: The commercial product is a mixture of isomers., Grade: 95%, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 10, 000 - <25, 2021: 10, 2020: 10, 1-Dodecanethiol 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)., (1972) Greater than 4.54X10+5 grams, (1975) Probably greater than 1.36X10+6 grams, General Manufacturing Information: Rubber Product Manufacturing, Petroleum Lubricating Oil and Grease Manufacturing, Plastics Product Manufacturing, Synthetic Rubber Manufacturing, Plastics Material and Resin Manufacturing, Construction, All Other Chemical Product and Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, 1-Dodecanethiol: ACTIVE, Thiols can be prepared by a variety of methods. The most-utilized of these synthetic methods for tertiary and secondary thiols is acid-catalyzed synthesis, for normal and secondary thiols, the most-utilized methods are free-radical-initiated, alcohol substitution, or halide substitution, for mercaptoalcohols, the most-utilized method is oxirane addition, and for mercaptoacids and mercaptonitriles, the most-utilized methods are Michael-type additions., Thiols.
TRIS(DODECYLTHIO)ANTIMONY is a carbon-based organic compound with CAS registry number 6939-83-9 and molecular formula C12H26S (molecular weight 202.40), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 6939-83-9
Its molecular formula C12H26S comprises 12 C, 26 H, 1 S atoms.
Also known as: TRIS(DODECYLTHIO)ANTIMONY · 三(十二硫基)锑
Category: organic chemicals
The CAS registry number of TRIS(DODECYLTHIO)ANTIMONY is 6939-83-9.
Molecular formula C12H26S, molecular weight 202.40.
It is also registered under: TRIS(DODECYLTHIO)ANTIMONY, 三(十二硫基)锑.
Recorded applications: Uses: Used in the production of drugs, insecticides, detergents, and synthetic rubber and as a flotation agent for metal refining, [ACGIH], Metal Extraction and Refining [Category: Industry], Polymerization regulator for styrene-butadiene rubber, In chemical syntheses of bactericides, as complexing agent, such as for the removal of metals from wastes, In manufacture of synthetic rubber, plastics, pharmaceuticals, fungicides, nonionic detergent, Flotation reagent, Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Industry Uses: Flame retardant, Intermediate, Chain transfer agent, Lubricating agent, Antioxidant, Consumer Uses: Antioxidant, Methods of Manufacturing: Reaction of metallic hydrosulfide with n-dodecyl chloride, This mercaptan can be produced by action of hydrogen sulfide on lauryl alcohol or on dodecene., Formulations, Preparations: The commercial product is a mixture of isomers., Grade: 95%, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 10, 000 - <25, 2021: 10, 2020: 10, 1-Dodecanethiol 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)., (1972) Greater than 4.54X10+5 grams, (1975) Probably greater than 1.36X10+6 grams, General Manufacturing Information: Rubber Product Manufacturing, Petroleum Lubricating Oil and Grease Manufacturing, Plastics Product Manufacturing, Synthetic Rubber Manufacturing, Plastics Material and Resin Manufacturing, Construction, All Other Chemical Product and Preparation Manufacturing, All Other Basic Organic Chemical Manufacturing, 1-Dodecanethiol: ACTIVE, Thiols can be prepared by a variety of methods. The most-utilized of these synthetic methods for tertiary and secondary thiols is acid-catalyzed synthesis, for normal and secondary thiols, the most-utilized methods are free-radical-initiated, alcohol substitution, or halide substitution, for mercaptoalcohols, the most-utilized method is oxirane addition, and for mercaptoacids and mercaptonitriles, the most-utilized methods are Michael-type additions., Thiols.
Category: Organic Chemicals.
Independent reference data for TRIS(DODECYLTHIO)ANTIMONY (CAS 6939-83-9), compiled from public chemistry databases.
| CAS 号 | 6939-83-9 |
|---|---|
| PubChem CID | 8195 |
| 分子式 | C12H26S |
| IUPAC 名称 | dodecane-1-thiol |
| UNII（FDA） | S8ZJB6X253 |
| FEMA 编号 | 4581 |
| JECFA 编号 | 1924 |
| Molecular Weight | 202.40 |
|---|---|
| XLogP3 | 6.1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 10 |
| Exact Mass | 202.17552200 |
| Monoisotopic Mass | 202.17552200 |
| Topological Polar Surface Area | 1 |
| Heavy Atom Count | 13 |
| Boiling Point | 511 to 541 °F at 760 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | BP: 142-145 °C @ 15 MM HG |
| Boiling Point | 266-285 °C |
| Boiling Point | 142-143 °C (16 mm Hg) |
| Boiling Point | 441-478 °F |
| Melting Point | 19 °F (NTP, 1992) |
| Melting Point | -7 °C |
| Melting Point | -7 - -9 °C |
| Melting Point | 19 °F |
| Melting Point | 15 °F |
1-DODECANETHIOL; 112-55-0; Dodecyl mercaptan; Lauryl mercaptan; n-Dodecyl mercaptan; n-Dodecanethiol; 1-Mercaptododecane; n-Lauryl mercaptan; N-Dodecylmercaptan; 1-Dodecyl mercaptan; Pennfloat M; Dodecylmercaptan; 1-dodecylthiol; Pennfloat S; Lauryl mercaptide; M-Lauryl mercaptan
| 法规与食品接触 | FDA Substance added to food: FLAVORING AGENT OR ADJUVANT FDA 21 CFR 中列出的食品接触物质清单：FCS FLAVOURING_AGENT: Flavouring Agent Flavoring Agents Savory No safety concern at current levels of intake when used as a flavouring agent |
|---|---|
| GHS 通报统计 | 1% (11 / 1091) |
| GHS 通报统计 | 1% (11 / 1091) |
|---|---|
| 已通报的危害声明 | H302 (10.4%), H312 (10.4%), H314 (44.3%), H315 (26.7%), H317 (66.7%), H318 (53.3%), H319 (25.9%), H332 (10.4%) |
三(十二硫基)锑 · CAS 6939-83-9 · C12H26S. UNII S8ZJB6X253. Boiling Point: 511 to 541 °F at 760 mmHg (NTP, 1992); Boiling Point: BP: 142-145 °C @ 15 MM HG; Boiling Point: 266-285 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 三(十二硫基)锑