di(tridecyl) phthalate (CAS 119-06-2) — formula C34H58O4, molecular weight 530.8; category organic chemicals.
| CAS Number | 119-06-2 |
|---|---|
| Molecular Formula | C34H58O4 |
| Molecular Weight | 530.8 |
| Boiling Point | 285 °C at 3.5 mm Hg |
| LogP | 14.5 |
| Applications | Uses: Used as plasticizer for polyvinyl chloride in cable and high-temperature wire insulation, [HSDB], PLASTICIZER FOR POLYVINYL CHLORIDE FOR CABLE INSULATION, ELECTRICAL WIRE & BUILDING WIRE, Plasticizer in high temp wire compounds, Phthalate esters are mainly used as plasticizers, primarily used to soften polyvinyl chloride. They are found in a number of products, including glues, building materials, personal care products, detergents and surfactants, packaging, children's toys, paints, pharmaceuticals, food products, and textiles. Phthalates are used in a variety of household applications such as shower curtains, vinyl upholstery, adhesives, floor tiles, food containers and wrappers, and cleaning materials. Personal care items containing phthalates include perfume, eye shadow, moisturizer, nail polish, liquid soap, and hair spray. (L1903), Consumption Patterns: 100% AS A VINYL PLASTICIZER, U.S. Production: (1972) 1.09X10+10 G, (1975) 7.12X10+9 G, 1, 2-Benzenedicarboxylic acid, ditridecyl ester 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)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#1146], U.S. Imports: (1972) NEGLIGIBLE, (1974) 1.71X10+8 G, General Manufacturing Information: 1, 2-ditridecyl ester: ACTIVE, The first step, alcoholysis of phthalic anhydride (PA) to give the monoester, is rapid and goes to completion. The reaction generally starts at elevated temperatures and proceeds exothermically. The second step is the conversion of the monoester to a diester with the formation of water. This is a reversible reaction and proceeds more slowly than the first, thus determining the overall rate of reaction. To shift the equilibrium towards the diester, the water of reaction is removed by distillation. The rate of reaction can be influenced by the choice of catalyst and the reaction temperature. For fast conversion rates, high reaction temperatures are generally used. However, these are influenced by the boiling point of the alcohol and, or the type of catalyst. ... Currently, nearly all major phthalate producers use amphoteric catalysts for the esterification of high boiling alcohols. ... The reaction temperatures for the amphoteric catalysts are about 200 °C. At this temperature side reactions are minimized, and the alcohol can be recycled without purification. By using this type of catalyst, over 99.5 % conversion to diester can be achieved., Phthalates |
| Category | Organic Chemicals |
Documented applications: Uses: Used as plasticizer for polyvinyl chloride in cable and high-temperature wire insulation, [HSDB], PLASTICIZER FOR POLYVINYL CHLORIDE FOR CABLE INSULATION, ELECTRICAL WIRE & BUILDING WIRE, Plasticizer in high temp wire compounds, Phthalate esters are mainly used as plasticizers, primarily used to soften polyvinyl chloride. They are found in a number of products, including glues, building materials, personal care products, detergents and surfactants, packaging, children's toys, paints, pharmaceuticals, food products, and textiles. Phthalates are used in a variety of household applications such as shower curtains, vinyl upholstery, adhesives, floor tiles, food containers and wrappers, and cleaning materials. Personal care items containing phthalates include perfume, eye shadow, moisturizer, nail polish, liquid soap, and hair spray. (L1903), Consumption Patterns: 100% AS A VINYL PLASTICIZER, U.S. Production: (1972) 1.09X10+10 G, (1975) 7.12X10+9 G, 1, 2-Benzenedicarboxylic acid, ditridecyl ester 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)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#1146], U.S. Imports: (1972) NEGLIGIBLE, (1974) 1.71X10+8 G, General Manufacturing Information: 1, 2-ditridecyl ester: ACTIVE, The first step, alcoholysis of phthalic anhydride (PA) to give the monoester, is rapid and goes to completion. The reaction generally starts at elevated temperatures and proceeds exothermically. The second step is the conversion of the monoester to a diester with the formation of water. This is a reversible reaction and proceeds more slowly than the first, thus determining the overall rate of reaction. To shift the equilibrium towards the diester, the water of reaction is removed by distillation. The rate of reaction can be influenced by the choice of catalyst and the reaction temperature. For fast conversion rates, high reaction temperatures are generally used. However, these are influenced by the boiling point of the alcohol and, or the type of catalyst. ... Currently, nearly all major phthalate producers use amphoteric catalysts for the esterification of high boiling alcohols. ... The reaction temperatures for the amphoteric catalysts are about 200 °C. At this temperature side reactions are minimized, and the alcohol can be recycled without purification. By using this type of catalyst, over 99.5 % conversion to diester can be achieved., Phthalates.
di(tridecyl) phthalate is a carbon-based organic compound with CAS registry number 119-06-2 and molecular formula C34H58O4 (molecular weight 530.8), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 119-06-2
Its molecular formula C34H58O4 comprises 34 C, 58 H, 4 O atoms.
Also known as: di(tridecyl) phthalate · 邻苯二甲酸二(十三烷基)酯
Category: organic chemicals
The CAS registry number of di(tridecyl) phthalate is 119-06-2.
Molecular formula C34H58O4, molecular weight 530.8.
It is also registered under: di(tridecyl) phthalate, 邻苯二甲酸二(十三烷基)酯.
Recorded applications: Uses: Used as plasticizer for polyvinyl chloride in cable and high-temperature wire insulation, [HSDB], PLASTICIZER FOR POLYVINYL CHLORIDE FOR CABLE INSULATION, ELECTRICAL WIRE & BUILDING WIRE, Plasticizer in high temp wire compounds, Phthalate esters are mainly used as plasticizers, primarily used to soften polyvinyl chloride. They are found in a number of products, including glues, building materials, personal care products, detergents and surfactants, packaging, children's toys, paints, pharmaceuticals, food products, and textiles. Phthalates are used in a variety of household applications such as shower curtains, vinyl upholstery, adhesives, floor tiles, food containers and wrappers, and cleaning materials. Personal care items containing phthalates include perfume, eye shadow, moisturizer, nail polish, liquid soap, and hair spray. (L1903), Consumption Patterns: 100% AS A VINYL PLASTICIZER, U.S. Production: (1972) 1.09X10+10 G, (1975) 7.12X10+9 G, 1, 2-Benzenedicarboxylic acid, ditridecyl ester 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)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#1146], U.S. Imports: (1972) NEGLIGIBLE, (1974) 1.71X10+8 G, General Manufacturing Information: 1, 2-ditridecyl ester: ACTIVE, The first step, alcoholysis of phthalic anhydride (PA) to give the monoester, is rapid and goes to completion. The reaction generally starts at elevated temperatures and proceeds exothermically. The second step is the conversion of the monoester to a diester with the formation of water. This is a reversible reaction and proceeds more slowly than the first, thus determining the overall rate of reaction. To shift the equilibrium towards the diester, the water of reaction is removed by distillation. The rate of reaction can be influenced by the choice of catalyst and the reaction temperature. For fast conversion rates, high reaction temperatures are generally used. However, these are influenced by the boiling point of the alcohol and, or the type of catalyst. ... Currently, nearly all major phthalate producers use amphoteric catalysts for the esterification of high boiling alcohols. ... The reaction temperatures for the amphoteric catalysts are about 200 °C. At this temperature side reactions are minimized, and the alcohol can be recycled without purification. By using this type of catalyst, over 99.5 % conversion to diester can be achieved., Phthalates.
Category: Organic Chemicals.
Independent reference data for di(tridecyl) phthalate (CAS 119-06-2), compiled from public chemistry databases.
| CAS Registry Number | 119-06-2 |
|---|---|
| PubChem CID | 8379 |
| Molecular formula | C34H58O4 |
| IUPAC name | ditridecyl benzene-1,2-dicarboxylate |
| UNII (FDA) | I7417R3544 |
| Molecular Weight | 530.8 |
|---|---|
| XLogP3 | 14.5 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 28 |
| Exact Mass | 530.43351033 |
| Monoisotopic Mass | 530.43351033 |
| Topological Polar Surface Area | 52.6 |
| Heavy Atom Count | 38 |
| Boiling Point | 285 °C at 3.5 mm Hg |
|---|---|
| Flash Point | 460 °F (NTP, 1992) |
| Flash Point | 470 °F (243 °C) (Open cup) |
| Density | 0.952 g/cu cm at 25 °C |
| Viscosity | 190 cP at 25 °C |
| Other Experimental Properties | Pour point -37 °C |
DITRIDECYL PHTHALATE; Nuoplaz; Staflex DTDP; Truflex DTDP; Bis(tridecyl) phthalate; 1-Tridecanol, phthalate; ditridecyl benzene-1,2-dicarboxylate; Jayflex DTDP; Di(tridecyl) phthalate; Phthalic acid, ditridecyl ester; 1,2-Benzenedicarboxylic acid, ditridecyl ester; Ditridecyl 1,2-benzenedicarboxylate; CCRIS 6197; HSDB 381; EINECS 204-294-3; BRN 2023076
| GHS notification summary | 100% (453 / 453) |
|---|
| GHS notification summary | 100% (453 / 453) |
|---|---|
| Reported hazard statements | H317, H373 |
This chemical does not meet GHS hazard criteria for 100% (453 of 453) of all reports.
Reported as not meeting GHS hazard criteria by 453 of 453 companies. For more detailed information, please visit ECHA C&L website.
di(tridecyl) phthalate · CAS 119-06-2 · C34H58O4. UNII I7417R3544. Boiling Point: 285 °C at 3.5 mm Hg; Flash Point: 460 °F (NTP, 1992); Flash Point: 470 °F (243 °C) (Open cup).
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 邻苯二甲酸二(十三烷基)酯