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TERSİYER DODESİL MERKAPTAN (TERT DODECYL MERCAPTAN)

TERT DODECYL MERCAPTAN

CAS NUMBER: 25103-58-6

EC NUMBER: 246-619-1

SYNONYMS:tert-Dodecanethiol; 2,3,3,4,4,5-Hexamethyl-2-hexanethiol; tert-Dodecylmercaptan; sulfole120; t-ddm; tert.Dodecanthiol;tert-Dodecyl Mercaptan ;tert-Dodecanethiol; Tert-dodecyl mercaptan;Lauryl mercaptan; Dodecyl mercaptan; TDM;t-ddm;sulfole120;Sulfol 120;Dodecanethiol;tert-Dodecanet;T-DODECANETHIOL;Ncgc00091163-01;tert-dodecylthiol;tert.Dodecanthiol; tert-Dodecanethiol, tert-Lauryl Mercaptan;tert-Dodecyl mercaptan; tert-Dodecylthiol; TERT-DODECANETHIOL; t-Dodecanethiol; t-Dodecylmercaptan; Sulfole 120; CCRIS 6030; t-DDM; 2,3,3,4,4,5; hexamethylhexane-2-thiol; terc.Dodecylmerkaptan [Czech]; EINECS 246-619-1; BRN 1738382; NCGC00091163-03; 2,3,3,4,4,5-Hexamethyl-2-hexanethiol; terc.Dodecylmerkaptan; AC1L1OFU; DSSTox_CID_5221; UNII-G00MDQ58TB; DSSTox_RID_77707; G00MDQ58TB; DSSTox_GSID_25221; SCHEMBL3332338; CHEMBL1325985; DTXSID1025221; YAJYJWXEWKRTPO-UHFFFAOYSA-NTox21_400018; AKOS015900250; LS-1066; NCGC00091163-01; NCGC00091163-02; NCGC00091163-04; CAS-25103-58-6; 3-01-00-01794 (Beilstein Handbook Reference); I14-10461; 119147-91-0; 90501-34-1; InChI=1S/C12H26S/c1-9(2)10(3,4)11(5,6)12(7,8)13/h9,13H,1-8H3; YAJYJWXEWKRTPO-UHFFFAOYSA-N; tert-Dodecanethiol; tert-Dodecanethiol; Mercaptan (tert-Dodecyl Mercaptan); tert-Dodecanethiol (mixture of isomers); tert-Lauryl Mercaptan (mixture of isomers); tert-Dodecanethiol; Alkyl Thiols, Materials Science, Micro/NanoElectronics, Self Assembly & Contact Printing, Self-Assembly Materials, Thiols; InChI=1S/C12H26S/c1-12(2,3)10-8-6-4-5-7-9-11-13/h13H,4-11H2,1-3H3; UVXGZLRXSOTRRS-UHFFFAOYSA-N; Decanethiol, 9,9-dimethyl-; Lauryl mercaptan, Dodecyl mercaptan; tert-Dodecanethiol (mixture of isomers) for synthesis; TDM, Tert-Dodecanethiol; 2,3,3,4,4,5-HEXAMETHYL-2-HEXANETHIOL; SULFOLE 120; T-DDM; T-DODECANETHIOL; T-DODECYLMERCAPTAN, TERT-DODECANETHIOL; TERT-DODECYL MERCAPTAN; TERT-DODECYL THIOL, TERT-DODECYLMERCAPTAN; TERT-DODECYLTHIOL; TERT-LAURYL MERCAPTAN; C12H26S; tert-Dodecyl Mercaptan; tert-Dodecyl mercaptan, ethoxylated;tert-Dodecylthio poly(ethyleneoxy) ethanol; tert-Dodecyl mercaptan, ethoxylated; tert-Dodecyl mercaptan, ethoxylated;tert-Dodecylthio poly(ethyleneoxy) ethanol; Sphalerite flotationTert dodecyl mercaptanDensity functional theory; tert-Dodecyl Mercaptan; tert dodecyl mercaptan wiki; tert-dodecylmercaptaN; tert-Dodecylthiol 0.97; tert-Dodecylthiol 98%; dodecanthiol 98.00% ; tert-Dodecanethiol 98+% ; tert-Dodecylthiol; tert-Dodecyl mercaptan; Tert Dodecyl Mercaptan,99.00 Grade A, 99.00 Grade A *; tert-Dodecanethiol_(mixture of isomers); ; Lauryl mercaptan; Dodecyl mercaptan; tert-Dodecanethiol; tert-Dodecyl mercaptane; tert-Dodecanethiol (mixture ofisomers); tert dodecylmercaptan ; tert-Dodecylthio 92%; tert-Dodecyl mercaptan; tert-dodecylthiol 98.0%; tert-dodecylthiol2,3,3,4,4,5-hexamethyl-2-hexanethiol; tert-Dodecylthiol 99%; tert-Dodecyl mercaptan; Sulfide Palladium Acetophenone Hydrochloric Acid Solution Mercaptan ; PEG TERT-DODECYL THIOETHER; ALPHA-(2-(TERT-DODECYLTHIO)ETHYL)-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); DODECYLTHIOL, TERT-, ETHOXYLATED; DODECYL MERCAPTAN, TERT-, ETHOXYLATED; PEG TERT-DODECANETHIOL; POLY(OXY-1,2-ETHANEDIYL), ALPHA-(2 (TERT DODECYLTHIO)ETHYL)-OMEGA-HYDROXY- TERT-DODECYL MERCAPTAN, ETHOXYLATED; t-dodecanethiol; 2,2,4,6,6-Pentamethyl-4-heptanethiol [ACD/IUPAC Name]; 2,2,4,6,6-Pentaméthyl-4-heptanethiol [French] [ACD/IUPAC Name]; 2,2,4,6,6-Pentamethyl-4-heptanthiol [German] [ACD/IUPAC Name]; 2,2,4,6,6-Pentamethylheptane-4-thiol; 25103-58-6 [RN]; 296-714-7 [EINECS]; 4-Heptanethiol, 2,2,4,6,6-pentamethyl- [ACD/Index Name]; MFCD00043233 [MDL number]; tert-Dodecylmercaptan; tert-Dodecanethiol; tert-Dodecanethiol (mixture of isomers); tert-dodecylthiol; tert-Dodecyl mercaptan; tert-Dodecylthiol; TERT-DODECANETHIOL; t-Dodecanethiol; t-Dodecylmercaptan; Sulfole 120; CCRIS 6030; t-DDM; 2,3,3,4,4,5; hexamethylhexane-2-thiol; terc.Dodecylmerkaptan [Czech]; EINECS 246-619-1; BRN 1738382; NCGC00091163-03; 2,3,3,4,4,5-Hexamethyl-2-hexanethiol; terc.Dodecylmerkaptan; AC1L1OFU; DSSTox_CID_5221; UNII-G00MDQ58TB; DSSTox_RID_77707; G00MDQ58TB; DSSTox_GSID_25221; SCHEMBL3332338; CHEMBL1325985; DTXSID1025221; YAJYJWXEWKRTPO-UHFFFAOYSA-N; Tox21_400018; AKOS015900250; LS-1066; NCGC00091163-01; NCGC00091163-02; NCGC00091163-04; CAS-25103-58-6; 3-01-00-01794 (Beilstein Handbook Reference); I14-10461; 119147-91-0; 90501-34-1; InChI=1S/C12H26S/c1-9(2)10(3,4)11(5,6)12(7,8)13/h9,13H,1-8H3; YAJYJWXEWKRTPO-UHFFFAOYSA-N; tert-Dodecanethiol; tert-Dodecanethiol; Mercaptan (tert-Dodecyl Mercaptan); tert-Dodecanethiol (mixture of isomers); tert-Lauryl Mercaptan (mixture of isomers); tert-Dodecanethiol; Alkyl Thiols, Materials Science, Micro/NanoElectronics, Self Assembly & Contact Printing, Self-Assembly Materials, Thiols; InChI=1S/C12H26S/c1-12(2,3)10-8-6-4-5-7-9-11-13/h13H,4-11H2,1-3H3; UVXGZLRXSOTRRS-UHFFFAOYSA-N; Decanethiol, 9,9-dimethyl-; Lauryl mercaptan, Dodecyl mercaptan; tert-Dodecanethiol (mixture of isomers) for synthesis; TDM, Tert-Dodecanethiol; 2,3,3,4,4,5-HEXAMETHYL-2-HEXANETHIOL; SULFOLE 120; T-DDM; T-DODECANETHIOL; T-DODECYLMERCAPTAN, TERT-DODECANETHIOL; TERT-DODECYL MERCAPTAN; TERT-DODECYL THIOL, TERT-DODECYLMERCAPTAN; TERT-DODECYLTHIOL; TERT-LAURYL MERCAPTAN; C12H26S; tert-Dodecyl Mercaptan; tert-Dodecyl mercaptan, ethoxylated;tert-Dodecylthio poly(ethyleneoxy) ethanol; tert-Dodecyl mercaptan, ethoxylated; tert-Dodecyl mercaptan, ethoxylated;tert-Dodecylthio poly(ethyleneoxy) ethanol; Sphalerite flotationTert dodecyl mercaptanDensity functional theory; tert-Dodecyl Mercaptan; tert dodecyl mercaptan wiki; tert-dodecylmercaptaN; tert-Dodecylthiol 0.97; tert-Dodecylthiol 98%; dodecanthiol 98.00% ; tert-Dodecanethiol 98+% ; tert-Dodecylthiol; tert-Dodecyl mercaptan; Tert Dodecyl Mercaptan,99.00 Grade A, 99.00 Grade A *; tert-Dodecanethiol_(mixture of isomers); ; Lauryl mercaptan; Dodecyl mercaptan; tert-Dodecanethiol; tert-Dodecyl mercaptane; tert-Dodecanethiol (mixture ofisomers); tert dodecylmercaptan ; tert-Dodecylthio 92%; tert-Dodecyl mercaptan; tert-dodecylthiol 98.0%; tert-dodecylthiol2,3,3,4,4,5-hexamethyl-2-hexanethiol; tert-Dodecylthiol 99%; tert-Dodecyl mercaptan; Sulfide Palladium Acetophenone Hydrochloric Acid Solution Mercaptan ; PEG TERT-DODECYL THIOETHER; ALPHA-(2-(TERT-DODECYLTHIO)ETHYL)-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); DODECYLTHIOL, TERT-, ETHOXYLATED; DODECYL MERCAPTAN, TERT-, ETHOXYLATED; PEG TERT-DODECANETHIOL; POLY(OXY-1,2-ETHANEDIYL), ALPHA-(2 (TERT DODECYLTHIO)ETHYL)-OMEGA-HYDROXY- TERT-DODECYL MERCAPTAN, ETHOXYLATED; t-dodecanethiol; 2,2,4,6,6-Pentamethyl-4-heptanethiol [ACD/IUPAC Name]; 2,2,4,6,6-Pentaméthyl-4-heptanethiol [French] [ACD/IUPAC Name]; 2,2,4,6,6-Pentamethyl-4-heptanthiol [German] [ACD/IUPAC Name]; 2,2,4,6,6-Pentamethylheptane-4-thiol; 25103-58-6 [RN]; 296-714-7 [EINECS]; 4-Heptanethiol, 2,2,4,6,6-pentamethyl- [ACD/Index Name]; MFCD00043233 [MDL number]; tert-Dodecylmercaptan; tert-Dodecanethiol; tert-Dodecanethiol (mixture of isomers); tert-dodecylthiol; tert-Dodecyl mercaptan, ethoxylated;tert-Dodecylthio pol (ethyleneoxy) ethanol; Sphalerite flotationTert dodecyl mercaptanDensity functional theory; 2,2,4,6,6-pentamethyl-4-heptanethiol (major, representative component), tert-dodecylmercaptan, tert-laurylmercaptan, TDM, tert-DDM, Sulfole®120; Sulfide Palladium Acetophenone Hydrochloric Acid Solution Mercaptan; tert dodecil merkaptan; tersiyer dodesil merkaptan; tersıyer dodesıl merkaptan; tersıyer dodesil merkaptan; tersiyer dodesıl merkaptan; tert dodecyl mercaptan; tert dodsil merkaptan; tert dodecyl mercaptan; TERT DODECYL MERCAPTAN; TERSİYER DODECYŞ MERCAPTAN; TERSIYER DODESIL MERKAPTAN; TERSİYER DODESİL MERKAPTAN; TERSIYER DODESİL MERKAPTAN; TERSİYER DODESIL MERKAPTAN; TERT DODECYL MERCAPTAN; PEG-9-10 TERT-DODECYL THIOETHER; DODECYLTHIOL, TERT-, ETHOXYLATED (9-10 MOLES); DODECYL MERCAPTAN, TERT-, ETHOXYLATED (9-10 MOLES); PEG-9-10 TERT-DODECANETHIOL; TERT-DODECANETHIOL, ETHOXYLATED (9-10 MOLES); TERT-DODECYL MERCAPTAN, ETHOXYLATED (9-10 MOLES); tert Dodecylmercaptan;Sulfole 120;t-DDM;tert-Dodecyl Thiol;tert-Lauryl Mercaptan;2,3,3,4,4,5-Hexamethyl-2-hexanethiol;2,3,3,4,4,5-Hexamethylhexane-2-thiol;tert-Dodecylthiol;Tertiary Dodecyl Mercaptan;tert-Dodecyl Mercaptan;tert-Dodecanethiol;Tertiary Dodecyl Mercaptan;Tert Dodecyl Mercaptan; Tert-dodecyl mercaptan; tert-Dodecanethiol (mixture of isomers); dodecanethiol, mixed isomers; 2,3,3,4,4,5-hexamethylhexane-2-thiol; tert-Dodecanethiol; n-Dodecyl mercaptan; Dodecyl mercaptan; Lauryl mercaptan; Mercaptan C12; NDM; 1-Dodecanethiol; CH3(CH2)11SH; 202.40; 969337; MFCD00004885; tert-Dodecyl mercaptan; TERT-DODECANETHIOL; tert-Dodecylthiol; t-Dodecanethiol; t-Dodecylmercaptan; Sulfole 120; CCRIS 6030; t-DDM; 2,3,3,4,4,5-hexamethylhexane-2-thiol; terc.Dodecylmerkaptan [Czech]; 1,3,3,4,4,5-Hexamethyl-2-hexanethiol; EINECS 246-619-1; BRN 1738382; NCGC00091163-03; terc.Dodecylmerkaptan; AC1L1OFU; DSSTox_CID_5221; UNII-G00MDQ58TB; DSSTox_RID_77707; G00MDQ58TB; DSSTox_GSID_25221; SCHEMBL3332338; CHEMBL1325985; DTXSID1025221; YAJYJWXEWKRTPO-UHFFFAOYSA-N; Tox21_400018; AKOS015900250; LS-1066; NCGC00091163-01; NCGC00091163-02; NCGC00091163-04; LP082215; OR050371; CAS-25103-58-6; 3-01-00-01794; (Beilstein Handbook Reference); I14-10461; 119147-91-0; 90501-34-1; C12H26S; 1-Dodécanethiol; 1-Dodecanthiol; Pennfloat M; Pennfloat S; UNII:S8ZJB6X253; WNAHIZMDSQCWRP-UHFFFAOYSA-N; dodesil; dodesil merkaptan; merkaptan; dodecil; dodecil mercaptan; dodecyl mercaptane; dodesil mercaptane; dodecyl merkaptan; dodecyl merkaptane; dodesil merkaptane

Tersiyer dodesil merkaptan (TDM), üretim sürecinde yaygın olarak bir zincir transfer maddesi olarak kullanılır. Halı ve kağıt endüstrisinde kullanım için stiren / bütadien lateks. Bir gaz kromatografisi tekniği başarıyla gerçekleştirilmiştir. Malzeme tanımlaması, trend analizi için kükürt içeriğine dayalı TDM ölçümü için veya Nihai ürünlerdeki reaksiyona girmemiş kalıntı malzemenin izlenmesi. Yöntem düşük termal kütle gaz kromatografisi (LTM-) kullanır.GC) ve bir çift-plazma kükürt kemilüminesans detektörü (DP-SCD), yüksek bir hassasiyet ve seçicilik derecesi elde etmek için. Tarif edilen teknik kullanılarak, 0.5 ppm (v / v) TDM aralığında ve 1 dakikadan az analiz süresinde bir tespit limiti olabilir elde etti. Yanıt,% 5`ten daha az RSD`nin yüksek tekrarlanabilirlik derecesine sahip dört büyüklük derecesi üzerinde doğrusaldır. İçinde Stiren-butadien gibi lateks imalat prosesi, bir zincir transfer ajanı gereklidir. Zincir aktarımı ajan, istenen moleküler dağılımın ürünlerini yapmak için polimerizasyonda yardımcı olur. Daha önce klorlu bu uygulama için karbon tetraklorür ve kloroform gibi bileşikler kullanılmıştır, ancak toksisiteleri nedeniyle ve olumsuz çevresel etkiler, artık kullanılan lateks üretimi için söz konusu bileşiklerin kullanılması bir uygulamadır. Halı ve kağıt endüstrisi için. Bunun yerine, uygulamalar için tersiyer dodesil merkaptan (TDM) kullanılması tercih edilir tanımladı. Dünya lateks talebi ve ilgili endüstrilerin büyüklüğü nedeniyle, TDM bir endüstriyel önemi olan kimyasallar.

Önemli

-TDM, daha az CuSO4 ve frother içermeyen sfalerit için etkili bir toplayıcıdır.

-Mineraller yüzeyinde TDM kemisorbs.

-TDM`nin mineral yüzeyler üzerindeki adsorpsiyon modları, ilk prensip çalışması ile elde edilir.

-TDM`nin ZnS (110) ve FeS2 (100) üzerindeki soğurma enerjileri ⿿394.78, 19219.33 kJ / mol`dür.

-Sürümler S 3p orbital TDM ve Zn / Fe minerallerinin orbitalleri arasında gerçekleşir.

Sfaleritin flotasyonunda, sülfidik (pirit) ve sülfürik olmayan gang (silika) minerallerinin eşzamanlı flotasyonu Şamandıra konsantresinin derecesini önemli ölçüde azaltır. Araştırma için laboratuvar ölçeği deneyleri yapılmıştır.Tert dodesil merkaptanın (TDM) bir toplayıcı olarak sfaleritin flotasyonuna etkisi. Sadece 160 g / t ilavesi Şu anda xanthate reaktif şemasında kullanılanın% 30`u olan bakır sülfat, kurtarma. Pirit ile ilgili olarak sfalerit için seçicilik, bakır sülfat olduğunda önemli ölçüde geliştirilmiştir. Deprem olarak kireç ile eklenir ve sonuçlar pH 9⿿10.5 de elde edilebilir. Elde edilen sonuçlara göre, tert dodesil merkaptanın sfalerit ile etkileşimi adsorpsiyon ölçümü, fourier dönüşümü ile araştırılmıştır.Kızılötesi (FTIR) ve yoğunluk fonksiyonel teorisi (DFT). TDM`nin sfalerit yüzeyinde kimyasal olarak adsorbe olduğu gösterilmiştir.FTIR testlerinde bazı karakteristik pikler sfalerit yüzeyinde ortaya çıkmış ve göç etmişlerdir. Butilxanthate ile karşılaştırıldığında, bir TDM ve sfalerit arasındaki daha güçlü etkileşim, sınır yörüngesinin enerji hesaplamasının analizi ile belirlenir. Bu ayrıca, adsorpsiyon enerji hesaplaması ile TDM ve ZnS (110) yüzeyi arasında güçlü bir etkileşimin, enerji ⿿394,78 kJ / mol. TDM üzerindeki S 3p yörüngesi ZnS (110) yüzeyinde Zn 3d orbital ile kuvvetli bir şekilde etkileşti ve Zn atomundan O atomuna aktarılan elektronlar, pozitif bir koordinat bağı ile sonuçlandı. Tersiyer dodesil merkaptan veya TDM, izobütilen trimeri veya propilen tetramerin oligomerlerinden elde edilen izometrik tiyollerin bir kombinasyonudur. Üreticiler bu ikisinden birini seçer ve hidrojen sülfür ile karıştırır, sonra karışımı bor gibi bir katalizör üzerinden geçirirler. TDM üretmek için trifluoride. Kısa bir süre önce zincir aktarımı olarak kullanılması nedeniyle önemli bir endüstriyel kimyasal haline gelmiştir.Lateks üretiminde ajan. Bir ajan olarak, son ürünlerin polimerizasyonunda yardımcı olur. Bu rol eskiden kloroform, karbon tetraklorür ve diğer klorlu bileşiklere verilir. Ancak, toksisite ve ekolojik ekolojik çarpışma endüstrinin alternatifler aramasını sağladı. Bu kimyasal ayrıca aşağıdaki isimlerle gider: tert-Dodecyl mercaptan, TERT-DODECANETHIOL, t-Dodecanethiol, Sulfole 120, tert-Dodesiltiol, CCRIS 6030 ve t-DDM. Ara madde olarak kullanılır. Bir proses regülatörü olarak ve yağlayıcılara bir katkı maddesi olarak. Bu, itici bir kokuya sahiprenksiz bir sıvı olarak görünür.

Tertiary dodecyl mercaptan (TDM) is commonly used as a chain transfer agent in the manufacturing process of styrene/butadiene latex for use in carpet and paper industries. A gas chromatographic technique has been successfully developed for the measurement of TDM based on its sulfur content for material identification, trend analysis, or for the monitoring of un-reacted residual material in final products. The method employs low thermal mass gas chromatography (LTM-GC) and a dual-plasma sulfur chemiluminescence detector (DP-SCD) to attain a high degree of sensitivity and selectivity. Using the technique described, a detection limit in the range of 0.5 ppm (v/v) TDM and less than 1 min analysis time can be achieved. Response is linear over four orders of magnitude with high degree of repeatability of less than 5% RSD. In the process of manufacturing latex such as styrene-butadiene, a chain transfer agent is required. The chain transfer agent assists in the polymerization to make products of the desired molecular distribution. Previously, chlorinated compounds such as carbon tetrachloride and chloroform have been used for this application, but because of their toxicity and negative environmental effects, it is no longer a practice to employ said compounds for the manufacturing of latex used for the carpet and paper industries. Instead, use of tertiary dodecyl mercaptan (TDM) is preferred for the applications described. As a result of the world demand for latex and the magnitude of the associated industries, TDM has become a chemical of industrial significance.

Highlights

-TDM is an effective collector for sphalerite with less CuSO4 and without frother.

-TDM chemisorbs on the minerals surface.

-Adsorption modes of TDM on mineral surfaces are obtained by first-principle study.

-Absorption energies of TDM on ZnS (110) and FeS2 (100) are ⿿394.78, ⿿219.33 kJ/mol.

-Reactions happen between S 3p orbital of TDM and 3d of Zn/Fe orbital of minerals.

In the flotation of sphalerite, the concomitant flotation of sulfidic (pyrite) and nonsulfidic gangue (silica) minerals significantly reduces the grade of the float concentrate. Laboratory scale experiments have been conducted to investigate the effect of tert dodecyl mercaptan (TDM) as a collector on the flotation of sphalerite. The addition of only 160 g/t copper sulfate, which is ⿼30% of that which is being used currently in the xanthate reagent scheme, improves the grade and the recovery. The selectivity for sphalerite, with respect to pyrite, has been improved significantly when copper sulfate is added with lime as the depressant, and the results could be achieved at pH 9⿿10.5.Based on the results obtained, the interaction of tert dodecyl mercaptan with sphalerite has been investigated by adsorption measurement, fourier transform infrared (FTIR) and density functional theory (DFT). It is showed that, TDM adsorbed on sphalerite surface chemically with some characteristic peaks appeared and migrated on sphalerite surface in FTIR tests. Compared with butyl xanthate, a stronger interaction between TDM and sphalerite is determined by analyses of frontier orbital energy calculation. It is also indicated that, by adsorption energy calculation, a strong interaction between TDM and ZnS (110) surface occurs, with the energy ⿿394.78 kJ/mol. The S 3p orbital on TDM interacted strongly with Zn 3d orbital on ZnS (110) surface, and electrons transferred from the Zn atom to the O atom, which resulted in a positive coordinate bond formed. Tertiary dodecyl mercaptan or TDM is a combination of isometric thiols obtained from oligomers of isobutylene trimer or propylene tetramer. Manufacturers pick one of these two and mix it with hydrogen sulfide, then pass the mixture over a catalyst like boron trifluoride to produce TDM. It has recently become a significant industrial chemical because of its use as a chain transfer agent in the manufacture of latex. As an agent, it helps in the polymerization of the end products. This role used to be given to chloroform, carbon tetrachloride, and other compounds of chlorine. However, their toxicity and negative ecological impact made the industry look for alternatives. This chemical also goes by the following names: tert-Dodecyl mercaptan, TERT-DODECANETHIOL, t-Dodecanethiol, Sulfole 120, tert-Dodecylthiol, CCRIS 6030, and t-DDM. It is used as an intermediate, as a process regulator, and as an additive to lubricants. This appears as a colorless liquid with a repulsive odor.

TERSİYER DODESİL MERKAPTAN (TERT DODECYL MERCAPTAN)

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