1-9 A-D E-G H-M N-P Q-S T-Z

TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM CHLORIDE (THPC)

TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM CHLORIDE (THPC)
CAS NUMBER: 124-64-1
EC NUMBER: 204-707-7


SYNONYMS: Tetrakis(hydroxymethyl)phosphonium chloride solution; 124-64-1; Linear Formula (HOCH2)4PCl; 190.56; 3631669; MFCD00031687; AKXUUJCMWZFYMV-UHFFFAOYSA-M; 80% in H2O; Tetrakis(hydroxymethyl)phosphonium chloride solution; 3631669; 24865276; (HOCH2)4PCl; Tetrakis(hydroxymethyl)phosphonium chloride solution, 80% in H2O; Tetra(hydroxymethyl)phosphonium chloride; 190.562; 190.016174 Da; 29038; Chlorure de tétrakis(hydroxyméthyl)phosphonium [French] [ACD/IUPAC Name]; Phosphonium, tetrakis(hydroxymethyl)-, chloride (1:1) [ACD/Index Name]; Tetra(hydroxymethyl)phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride [ACD/IUPAC Name]; Tetrakis(hydroxymethyl)phosphoniumchlorid [German] [ACD/IUPAC Name]; [tris(hydroxymethyl)phosphino]methan-1-ol, chloride; 124-64-1 [RN]; 204-707-7 [EINECS]; 2245-60-5 [RN]; 52221-67-7 [RN]; 55566-30-8 [RN]; 7580-37-2 [RN]; EINECS 204-707-7; MFCD00031687 [MDL number]; Phosphonium, chloro-tetrakis(hydroxymethyl)-; phosphonium, tetrakis(hydroxymethyl)-, chloride; Proban CC; Pyroset TKC; Retardol C; Tetra(hydroxymethyl)phosphoniumchloride; Tetrahydroxymethylphosphonium chloride; TETRAKIS(HYDROXYMETHYL) PHOSPHONIUM CHLORIDE; Tetrakis(Hydroxymethyl) Posphonium Chloride; Tetrakis-(hydroxymethyl)fosfoniumchlorid [Czech]; Tetrakis-(hydroxymethyl)Fosfoniumchlorid [Czech]; tetrakis(hydroxymethyl)phosphanium chloride; Tetrakis(hydroxymethyl)phosphochloride; tetrakis(hydroxymethyl)-phosphonium chloride; tetrakis-(hydroxymethyl)-phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium Chloride (ca. 80% in Water); Tetrakis(hydroxymethyl)phosphonium chloride solution; Tetrakis(hydroxymethyl)phosphonium chloride;THPC; Tetrakis(hydroxymethyl)phosphonium phosphate tetrakis(hydroxymethyl)phosphoniumchloride; tetrakishydroxymethyl phosphonium chloride; tetrakishydroxymethylphosphonium chloride; TETRAMETHYLOLPHOSPHONIUM CHLORIDE; THPC; UNII:58WB2XCF8I; UNII-58WB2XCF8I; WLN: Q1P1Q1Q1Q & G; Tetrakis(hydroxymethyl)phosphonium chloride solution (CAS 124-64-1); CAS: 124-64-1, MF: (HOCH2)4PCl, MW: 190.56; Tetrakis(hydroxymethyl)phosphonium chloride solution; Tetrakis(hydroxymethyl)phosphonium Chloride (ca. 80% in Water); MFCD00031687; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride, ca. 80% solution in water; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride; MFCD00031687; Tetrakis(Hydroxymethyl)Phosphonium Chloride on Wool; TETRAKIS(HYDROXYMETHYL)-PHOSPHONIUM CHLORIDE UPON ACID HYDROLYSIS; tetrakis-hydroxymethyl-phosphonium-chloride-80-aqueous-solution; Tetramethylolphosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride, ca. 80%; 124-64-1,7732-18-5; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis (hydroxymethyl) phosphonium chloride; InChI=1S/C4H12O4P.ClH/c5-1-9(2-6,3-7)4-8;/h5-8H,1-4H2;1H/q+1;/p-1; AKXUUJCMWZFYMV-UHFFFAOYSA-M; 190.562; Tetrakis (hydroxymethyl) phosphonium chloride from phosphine and formaldehyde; Tetrakis(hydroxymethyl)phosphonium chloride, ca. 80% solution in water; Tetrakis(hydroxymethyl)phosphonium chloride, ca. 80% solution in water; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis(hydroxymethyl)phosphonium chloride; tetramethylolphosphonium chloride; THPC; TKC; 204-707-7; Tetrakis(hydroxymethyl) phosphonium chloride (THPC); Tetrakis(hydroxymethyl) phosphonium chloride ca. 80% solution in water; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrahydroxymethylphosphonium chloride, THPC; Tetrakis(hydroxymethyl)phosphonium chloride - CAS # 124-64-1; Tetrakis(hydroxymethyl)phosphonium chloride; C4H12ClO4P; 124-64-1; THPC; Tetramethylolphosphonium chloride; Proban CC; Tetrakis(hydroxymethyl)phosphochloride; etrakis(hydroxymethyl)phosphonium chloride; TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM CHLORIDE; Tetrakis Hydroxymethyl Phosphonium Chloride (THPC); Tetrakis Hydroxymethyl Phosphonium Chloride-Urea (THPC-U); Tetrakis(hydroxymethyl)fosfoniumchloride; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis-Hydroxymethyl Phosphonium Chloride (THPC); Tetrakis(hydroxymethyl)phosphonium chloride (THPC); Tetrakis(hydroxymethyl)phosphonium chloride ureapolymer; MFCD09263723; Tetrakis(hydroxymethyl)phosphonium chloride urea polymer; Tetrakis(hydroxymethyl)phosphonium chloride urea polymer | CAS Number: 27104-30-9; ACM27104309; THPC-Urea;tetrakis(hydroxymethyl)phosphonium chloride urea polymer;TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM PRECONDENSATE; TetrakisHydroxymethylPhosphoniumChloride-Urea(Thpc-U); Oligomertetrakis(hydroxymethyl)phosphoniumchloride-urea; Tetrakis(hydroxymethyl)phosp; (C4H12O4P?CH4N2O?Cl)x; Tetrakis (hydroxymethyl) phosphonium chloride; tetrakis(hydroxymethyl)phosphonium chloride;Tetrakis (hydroxymethyl) phosphonium chloride;Tetrahydroxymethyl phosphonium chloride; THPC; TMPC; C4H12ClO4P; 1S/C4H12O4P.ClH/c5-1-9(2-6,3-7)4-8;/h5-8H,1-4H2;1H/q+1;/p-1; AKXUUJCMWZFYMV-UHFFFAOYSA-M; Tetrakis Hydroxymethyl Phosphonium Chloride(THPC); Tetramethylolphosphonium Chloride ; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrahydroxymethylphosphonium chloride; THPC; tetrakis(hydroxymethyl)phosphonium chloride - CAS 124-64-1; C4H12O4P?Cl;C4H12ClO4P; THPC; TETRA(HYDROXYMETHYL)PHOSPHONIUM CHLORIDE; TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM CHLORIDE; tetramethylolphosphonium chloride; AURORA KA-1157; nci-c55061; tetrakis(hydroxymethyl)phosphonium chloride; Name: tetrakis(hydroxymethyl)phosphonium chloride; 124-64-1; C10H24O12P2; 398.238; tetrakis(hydroxymethyl)phosphonium chloride; THPC; Tetramethylolphosphonium chloride; THPS-UPC; tetrakis(hydroxymethyl)phosphonium; bis[tetrakis(hydroxymethyl)phosphonium] sulfate; tetrakis(hydroxymethyl)phosphonium acetate; bis[tetrakis(hydroxymethyl)phosphonium] ethanedioate; Tetrakis-Hydroxymethyl Phosphonium Sulfate-Urea Pre-condensate Polymer; InChI=1/2C4H12O4P.C2H2O4/c2*5-1-9(2-6,3-7)4-8;3-1(4)2(5)6/h2*5-8H,1-4H2;(H,3,4)(H,5,6)/q2*+1;/p-2; tetrakis(hydroxymethyl)phosphonium chloride; C10H24O12P2; Tetrakis(hydroxymethyl)phosphonium chloride-urea (THPC-UREA); (CH2OH)3P+CH2NHCONHCH2P+(CH2OH)3; tetrakis(hydroxymethyl)phosphonium chloride-urea (THPC-UREA) C9O7H24P2Cl2N2 ,Content %; Tetrakis-Hydroxymethyl Phosphonium Chloride; Tetrakis(hydroxymethyl)phosphonium chloride; TETRAKIS (HYDROXYMETHYL) PHOSPHONIUM CHLORIDE FROM PHOSPHINE AND FORMALDEHYDE; Tetrakis(hydroxymethyl)phosphonium chloride; Tetrakis (hydroxymethyl) phosphonium chloride (THPC); Tetrakis(Hydroxymethyl)Phosphonium Chloride; MFCD00031687; AKXUUJCMWZFYMV-UHFFFAOYSA-M; C4H12ClO4P; tetramethylolphosphonium acetate;Tetramethylolphosphonium chloride; tetramethylolphosphonium hydroxide; etramethylolphosphonium nitrate; tetramethylolphosphonium oxalate (2:1)tetramethylolphosphonium phosphate (3:1); tetramethylolphosphonium sulfate (2:1); THPC; Tetrakis(hydroxymethyl)phosphonium chloride; 124-64-1; THPC; Pyroset TKC; Retardol C; NCI-C55061; TETRAMETHYLOLPHOSPHONIUM CHLORIDE; Tetra(hydroxymethyl)phosphonium chloride; UNII-58WB2XCF8I; Proban CC; Tetrakis(hydroxymethyl)phosphochloride; CCRIS 317; Phosphonium, tetrakis(hydroxymethyl)-, chloride; tetrakis(hydroxymethyl)phosphanium chloride; HSDB 2923; EINECS 204-707-7; Tetrahydroxymethylphosphonium chloride; SC 30698; AI3-22268; Tetrakis-(hydroxymethyl)fosfoniumchlorid [Czech]; Phosphonium, tetrakis(hydroxymethyl)-, chloride (1:1); pyrosettkc; TETRAKIS(HYDROXYMETHYL) PHOSPHONIUM CHLORIDE; aurora ka-1157; Tetrakis-(hydroxymethyl)fosfoniumchlorid; ACMC-1BPFQ; AC1L1LCW; DSSTox_CID_1330; C1Q1SP2; 58WB2XCF8I; DSSTox_RID_76085; DSSTox_GSID_21330; KSC492Q8N; SCHEMBL196471; Jsp001618; CHEMBL2131547; DTXSID5021330; CTK3J2886; AKXUUJCMWZFYMV-UHFFFAOYSA-M; MolPort-002-043-774; WLN: Q1P1Q1Q1Q & GLS-31; NSC30698; Tox21_302070; 7580-37-2 (unspecified acetate); ANW-43807; MFCD00031687; NSC-30698; AKOS015918384; Tetra(hydroxymethyl)Phosphoniumchloride; NE10887; RTR-003787; NCGC00164162-01; NCGC00255382-01; 2031-17-0 (phosphate[3:1]); 52221-67-7 (oxalate[2:1]); 55566-30-8 (sulfate[2:1]); AK115995; CAS-124-64-1; KB-61541; OR013154; OR243180; SC-80017; DB-007909; tetrakis-(hydroxymethyl)phosphonium chloride; TR-003787; FT-0081358; T-0631726; Phosphonium, chloro-tetrakis(hydroxymethyl)-Phosphonium,tetrakis(hydroxymethyl)-,chloride; ST51055809; EN300-19000; I14-8218; TETRA HYDROXYMETHYL)PHOSPHONIUM CHLORIDE 80% SOLN IN H2O; 2245-60-5; CB2166508; tetrakishidroksimetil fosfonyum klorür; tetrakishidroksimetil fosfonyumklor; tetrakishidroksimetil fosfonyum; tetrakishidroksimethyl fosfonyum; tetrakishidroksimethyl fosfonyum kloride; tetrakishidroksimethyl fosfonyum chlorit; tetrakishidroksimethyl fosfonyum klorit; THPC; thpc; TETRAKİS; tetrakis; hidroksimetil; fosfonyum; klorür; phosphonium; chloride; hydroxy; methyl; hydroxymethyl; thps; thpc; fosfonyum kulorit; tetrakishidroksimetilfosfonyumkuloride; kuloride

 

 

 

 


Tetrakis(hydroxymethyl)phosphonium chloride (THPC) is an organophosphorus compound with the chemical formula [P(CH2OH)4]Cl. The cation P(CH2OH)4+ is four-coordinate, as is typical for phosphonium salts. THPC has applications as a precursor to fire-retardant materials. THPC has industrial importance in the production of crease-resistant and flame-retardant finishes on cotton textiles and other cellulosic fabrics. A flame-retardant finish can be prepared from THPC by the Proban Process,[4] in which THPC is treated with urea. The urea condenses with the hydroxymethyl groups on THPC. The phosphonium structure is converted to phosphine oxide as the result of this reaction.

[P(CH2OH)4]Cl + NH2CONH2 › (HOCH2)2POCH2NHCONH2 + HCl + HCHO + H2 + H2O
This reaction proceeds rapidly, forming insoluble high molecular weight polymers. The resulting product is applied to the fabrics in a "pad-dry process." This treated material is then treated with ammonia and ammonia hydroxide to produce fibers that are flame-retardant. etrakis(hydroxymethyl)phosphonium chloride (THPC) is an organophosphorus compound with the chemical formula [P(CH2OH)4]Cl. The cation P(CH2OH)4+ is four-coordinate, as is typical for phosphonium salts. THPC has applications as a precursor to fire-retardant materials. THPC can condense with many other types of monomers in addition to urea. These monomers include amines, phenols, and polybasic acids and anhydrides. Tris(hydroxymethyl)phosphine, which is derived from tetrakis(hydroxymethyl)phosphonium chloride, is an intermediate in the preparation of the water-soluble ligand 1,3,5-triaza-7-phosphaadamantane (PTA). This conversion is achieved by treating hexamethylenetetramine with formaldehyde and tris(hydroxymethyl)phosphine. Tris(hydroxymethyl)phosphine can also be used to synthesize the heterocycle, N-boc-3-pyrroline by ring-closing metathesis using Grubbs' catalyst (bis(tricyclohexylphosphine)benzylidineruthenium dichloride ). N-Boc-diallylamine is treated with Grubbs' catalyst, followed by tris(hydroxymethyl)phosphine. The carbon-carbon double bonds undergo ring closure, releasing ethylene gas, resulting in N-boc-3-pyrroline.[7] The hydroxymethyl groups on THPC undergo replacement reactions when THPC is treated with ?,ß-unsaturated nitrile, acid, amide, and epoxides. For example, base induces condensation between THPC and acrylamide with displacement of the hydroxymethyl groups. (Z = CONH2)

[P(CH2OH)4]Cl + NaOH + 3CH2=CHZ › P(CH2CH2Z)3 + 4CH2O + H2O + NaCl
Similar reactions occur when THPC is treated with acrylic acid; only one hydroxymethyl group is displaced, however. Tetrakis(hydroxymethyl)phosphonium chloride (THPC) is an organophosphorus compound with the chemical formula [P(CH2OH)4]Cl. The cation P(CH2OH)4+ is four-coordinate, as is typical for phosphonium salts. THPC has applications as a precursor to fire-retardant materials. Physical and chemical properties, toxicokinetics, toxicological, epidemiological, and exposure data on tetrakis(hydroxymethyl) phosphonium chloride (THPC), which is one of the tetrakis(hydroxymethyl) phosphonium salts. Although other tetrakis(hydroxymethyl) phosphonium salts have been used as flame retardants, the subcommittee chose to focus its assessment on THPC because it has a large toxicology database and is the most toxic of the phosphate salts. The subcommittee used the toxicity and exposure information on THPC to characterize the health risk from exposure to THPC. The subcommittee also identified data gaps and recommended research relevant for determining the health risk from exposure to THPC. The physical and chemical properties of THPC are summarized in Table 18-1. THPC is a water-soluble tetrakis(hydroxymethyl) phosphonium salt (IARC 1990) that is a common ingredient in commercial flame-retardant (FR) formulations. Tetrakis(hydroxymethyl)phosphonium chloride reacts vigorously with oxidizers and alkalis. Reacts with cellulose.


PHYSICAL DESCRIPTION
Clear slightly viscous,colorless to yellow liquid (20% H2O solution).
Color: Crystalline; Clear light pink or yellow-green
Solubility: greater than or equal to 100 mg/mL at 68° F (NTP, 1992).
Corrosivity: Corrosive
Melting point:154°C
Boiling point:115°C/760mmHg
Density: 1.341 g/mL at 25 °C
refractive index: n20/D 1.512
form: Solution
Water Solubility >=10 g/100 mL at 20 ºC


Formulations/Preparations
May be used in combination with triethylolamine and urea (Roxel process) or with triethanolamine and tris(1-aziridinyl) phosphate oxide. When heated to decomposition it emits very toxic fumes of /phosphorous oxides & hydrogen chloridE. Tetrakis(hydroxymethyl)phosphonium chloride can be absorbed through the skin. THPC is produced by the reaction of formaldehyde, phosphine, and hydrochloric acid. THPC and its sulfur salt THPS are the predominant FR chemicals used for cotton apparel, especially children's sleepwear. THPC was the most widely used FR for cotton fabrics in the 1950s. About 1,000-5,000 tons of THPC was used in the United States in 1987. No studies were identified that investigated the dermal absorption of THPC or other tetrakis(hydroxymethyl) phosphonium salts by humans. Dermal application of THPC to rats resulted in body weight loss and death (Aoyama 1975), indicating that THPC is absorbed by this route. Ulsamer et al., citing a 1953 report by the Wisconsin Alumni Research Foundation, stated that THPC can be absorbed through the skin in large amounts (1.5 gm/kg). It is not clear whether this is a derived amount or one based on animal data. The subcommittee could not locate a copy of the 1953 report. Results indicate that if all of the THPC is released from the fabric into the air, THPC could be a toxic risk to persons entering the room. In reality, any FR that evaporated so rapidly would be useless in preventing upholstery flammability. Either THPC is much more strongly bound to the fabric than assumed in this scenario (so that the parameter γ in the analysis above is substantially less than unity), or the chemical is transformed during the application process. In either case, the emission rate would likely be controlled by some process other than diffusion through a boundary layer of air, as assumed here. The subcommittee believes that this exposure scenario provides no useful information about the potential toxicity of THPC vapors to humans associated with the emission of THPC vapors from treated furniture upholstery. Therefore, further investigation should be carried out to determine if exposure to THPC by this route poses a toxic risk to humans. These results suggest that the vapor inhalation scenario is unrealistic for THPC-treated furniture in a residential setting because evaporative loss of all THPC over 16 hr could not occur under normal conditions. Since THPC is chemically cross-linked within the treated upholstery, the vapor pressure of THPC is assumed to be the vapor pressure for the polymerized form. In the absence of any published data, it is assumed that the polymerized form of THPC will have a vapor pressure approaching zero. Thus, the vapor inhalation noncancer risk from THPC-treated fabric may be assumed to be minimal if not zero.


ACUTE/CHRONIC HAZARDS

Tetrakis(hydroxymethyl)phosphonium chloride may be corrosive. When heated to decomposition, it may emit very toxic fumes of POx, hydrogen chloride and bis(chloromethyl)ether. Decomposition of Tetrakis(hydroxymethyl)phosphonium chloride in an aqueous environment may produce phosphine, formaldehyde and hydrogen chloride. Tetrakis(hydroxymethyl)phosphonium chloride is probably combustible. Phosphonium describes a univalent radical, PH4, phosphorus analogous to ammonium. Quaternary phosphonium salts, obtained from tertiary alkylphosphines with the treatment with alkyl or aromatic halides, are replacing phase transfer catalysts and biocides functions for quaternary ammonium salts due to more effective performance and higher thermal stability. Phosphonium saltds are used as flame retardants in textile, especially cotton, and as cease and rot resistance agents in fabric. They acts as biocides against SRB (Sulphate reducing bacteria known as Desulfuvibrio Desulfuricans) which produce enzymes to accelerate the reduction reaction of sulphates to the corrosive hydrogen sulphide and causes corrosion of iron material in a water system. Phosphonium salts are used as epoxy curing agents. A variety of phosphine transition metal complexes including chiral complexes are synthesized as the very reactive and versatile homogeneous catalysts and stereospecific as well. Tetrakis(hydroxymethyl)phosphonium Chloride is used as a flame retardant in textiles. THPC acts as a biocide against SRB (Sulphate reducing bacteria known as Desulfuvibrio Desulfuricans) which produce enzymes to accelerate the reduction reaction of sulphates to the corrosive hydrogen sulphide and causes corrosion of iron material in a water system. When THPC acts as a corrosion inhibitor in circulating water system. It has been replaced by the sulfate compound because of its forming of carcinogenic compound.

 

 

 

 

 

 


Tetrakis (hidroksimetil) fosfonyum klorür (THPC), kimyasal formül [P (CH2OH) 4] Cl'ye sahip bir organofosfor bileşiğidir. P (CH2OH) 4+ katyonu fosfonyum tuzları için tipik olduğu gibi dört koordinatlıdır. THPC, yangın geciktirici materyallerin öncüsü olarak uygulamaları vardır. THPC, pamuklu tekstiller ve diğer selülozik kumaşlara kıvrıma dirençli ve alevi tutmayan kaplamalar üretiminde endüstriyel öneme sahiptir. Alev geciktirici bir yüzey, THPC'den Proba Process, [4] tarafından THPC'ye üre ile muamele edilerek hazırlanabilir. Üre, THPC üzerinde hidroksimetil gruplarıyla yoğunlaşır. Fosfonyum yapısı, bu reaksiyon sonucunda fosfin oksite dönüştürülür.

[P (CH2OH) 4] Cl + NH2CONH2> (HOCH2) 2POCH2NHCONH2 + HC1 + HCHO + H2 + H20
Bu reaksiyon hızla ilerleyerek çözünmeyen yüksek molekül ağırlıklı polimerler oluşturur. Nihai ürün, kumaşlara "pedin kuru süreci" ile uygulanır. Bu muamele edilen malzeme daha sonra alev geciktirici lifler üretmek için amonyak ve amonyak hidroksit ile muamele edilir. etrakis (hidroksimetil) fosfonyum klorür (THPC) kimyasal formülü [P (CH2OH) 4] Cl olan bir organofosfor bileşiğidir. P (CH2OH) 4+ katyonu fosfonyum tuzları için tipik olduğu gibi dört koordinatlıdır. THPC, yangın geciktirici materyallerin öncüsü olarak uygulamaları vardır. THPC, üreye ilaveten birçok başka monomer türü ile yoğunlaşabilir. Bu monomerlere aminler, fenoller ve polibazik asitler ve anhidritler dahildir. Tetrakis (hidroksimetil) fosfonyum klorurdan türetilen Tris (hidroksimetil) fosfin, suda çözünür 1,3,5-triaza-7-fosfadamantanın (PTA) hazırlanmasında kullanılan bir ara maddedir. Bu dönüşüm, hekzametilenetetaminin formaldehit ve tris (hidroksimetil) fosfin ile muamele edilmesiyle elde edilir. Tris (hidroksimetil) fosfin, Grubbs katalizörü (bis (trisikloheksilfosfin) benzilidinerutenyum diklorür) kullanılarak halka kapanış metateziyle heterohalkayı, N-boc-3-pirolini sentezlemek için de kullanılabilir. N-Boc-diallilamin Grubbs 'katalizörü, ardından tris (hidroksimetil) fosfin ile muamele edilir. Karbon-karbon çift bağları etilen gazı serbest bırakarak halka kapanır ve böylece N-boc-3-pirolin oluşur. [7] THPC üzerindeki hidroksimetil grupları, THPC, a, ß-doymamış nitril, asit, amid ve epoksitler ile muamele edildiğinde yer değiştirme reaksiyonlarına girerler. Örneğin, baz hidroksimetil gruplarının yer değiştirmesi ile THPC ve akrilamid arasında yoğunlaşmayı indükler. (Z = CONH2)

[P (CH2OH) 4] Cl + NaOH + 3CH2 = CH2> P (CH2CH2Z) 3 + 4CH2O + H20 + NaCl
THPC akrilik asit ile muamele edildiğinde benzer reaksiyonlar oluşur; Bununla birlikte, sadece bir hidroksimetil grubu yerinden edilmiştir. Tetrakis (hidroksimetil) fosfonyum klorür (THPC), kimyasal formül [P (CH2OH) 4] Cl'ye sahip bir organofosfor bileşiğidir. P (CH2OH) 4+ katyonu fosfonyum tuzları için tipik olduğu gibi dört koordinatlıdır. THPC, yangın geciktirici materyallerin öncüsü olarak uygulamaları vardır. Tetrakis (hidroksimetil) fosfonyum tuzlarından biri olan tetrakis (hidroksimetil) fosfonyum klorid (THPC) üzerindeki fiziksel ve kimyasal özellikler, toksikokinetik, toksikolojik, epidemiyolojik ve maruz kalma verileri. Alev geciktiriciler olarak diğer tetrakis (hidroksimetil) fosfonyum tuzları kullanılmış olsa da, alt komite, THPC'ye ilişkin değerlendirmesine odaklanmayı tercih etmiştir, çünkü büyük bir toksikoloji veritabanına sahiptir ve fosfat tuzlarının en toksiktir. Alt komite, THPC'ye maruz kalmadan sağlık riskini karakterize etmek için THPC üzerindeki toksisite ve maruz kalma bilgilerini kullandı. Alt komite aynı zamanda veri boşluklarını tespit etti ve THPC'ye maruz kalındığında sağlık riskini belirlemek için gerekli araştırma önerdi. THPC'nin fiziksel ve kimyasal özellikleri Tablo 18-1'de özetlenmiştir. THPC, ticari alev geciktirici (FR) formülasyonlarda ortak bir bileşen olan suda çözünür bir tetrakis (hidroksimetil) fosfonyum tuzudur (IARC, 1990). Tetrakis (hidroksimetil) fosfonyum klorür, oksitleyiciler ve alkaliler ile kuvvetli tepki verir. Selüloz ile reaksiyona girer.
Tetrakis (hidroksimetil) fosfonyum tuzlarından biri olan tetrakis (hidroksimetil) fosfonyum klorid (THPC) üzerindeki fiziksel ve kimyasal özellikler, toksikokinetik, toksikolojik, epidemiyolojik ve maruz kalma verileri. Alev geciktiriciler olarak diğer tetrakis (hidroksimetil) fosfonyum tuzları kullanılmış olsa da, alt komite, THPC'ye ilişkin değerlendirmesine odaklanmayı tercih etmiştir, çünkü büyük bir toksikoloji veritabanına sahiptir ve fosfat tuzlarının en toksiktir. Alt komite, THPC'ye maruz kalmadan sağlık riskini karakterize etmek için THPC üzerindeki toksisite ve maruz kalma bilgilerini kullandı. Alt komite aynı zamanda veri boşluklarını tespit etti ve THPC'ye maruz kalındığında sağlık riskini belirlemek için gerekli araştırma önerdi. THPC'nin fiziksel ve kimyasal özellikleri Tablo 18-1'de özetlenmiştir. THPC, ticari alev geciktirici (FR) formülasyonlarda ortak bir bileşen olan suda çözünür bir tetrakis (hidroksimetil) fosfonyum tuzudur (IARC, 1990). Tetrakis (hidroksimetil) fosfonyum klorür, oksitleyiciler ve alkaliler ile kuvvetli tepki verir. Selüloz ile reaksiyona girer.


FİZİKSEL TANIM
Hafifçe viskoz, renksiz ila sarı sıvıya temizleyin (% 20 H20 çözeltisi).
Renk: Kristalin; Açık pembe veya sarı-yeşil berrak
Çözünürlük: 68 ° F'da 100 mg / mL'den büyük veya eşit (NTP, 1992).
Koroziflik: Korozif
Erime noktası: 154 ° C
Kaynama noktası: 115 ° C / 760mmHg
Yoğunluk: 25 ° C'de 1.341 g / mL
kırma indisi: n20 / D 1.512
form: Çözüm
Suda Çözünürlük> = 10 g / 100 mL, 20 ºC'de

Trietilolamin ve üre (Roksel proses) veya trietanolamin ve tris (1-aziridinil) fosfat oksit ile kombinasyon halinde kullanılabilir. Parçalanmaya kadar ısıtıldığında, fosfor oksitler ve hidrojen klorid / toksik dumanlar yayar. Tetrakis (hidroksimetil) fosfonyum klorür deriden absorbe edilebilir. THPC, formaldehit, fosfin ve hidroklorik asit reaksiyonuyla üretilir. THPC ve sülfür tuzu THPS pamuklu giysiler, özellikle çocuk pijama için kullanılan baskın FR kimyasallarıdır. THPC 1950'lerde pamuklu kumaşlar için en yaygın olarak kullanılan FR idi. 1987'de Birleşik Devletlerde yaklaşık 1.000-5.000 ton THPC kullanıldı. İnsanlar tarafından THPC veya diğer tetrakis (hidroksimetil) fosfonyum tuzlarının dermal emilimini araştıran hiçbir çalışma tespit edilmemiştir. THPC'nin sıçanlara uygulanması, vücut ağırlığı kaybı ve ölüm ile sonuçlanmıştır (Aoyama 1975). THPK'nin bu yol tarafından absorbe edildiğini gösterir. Ulsamer ve arkadaşları, Wisconsin Mezun Araştırmaları Vakfı tarafından 1953 yılında hazırlanan bir rapora dayanarak, THPC'nin ciltten büyük miktarlarda (1.5 gm / kg) emilebileceğini belirtti. Bunun türetilmiş bir miktar olup olmadığı veya hayvan verilerine dayalı bir miktar olup olmadığı açık değildir. Alt komite 1953 raporunun bir kopyasını bulamadı. Sonuçlar, THPC'nin tamamının kumaştan havaya bırakılması halinde THPC'nin odaya giren kişilere toksik bir risk oluşturabileceğini göstermektedir. Gerçekte, bu kadar çabuk buharlaşan herhangi bir FR, döşemenin yanıcılığını önlemede yararsız olacaktır. THPC, bu senaryoda varsayıldığı kadar kumaşa çok daha fazla bağlıdır (yukarıdaki analizde γ parametresi esasen birlikten daha düşüktür) veya kimyasal uygulama işlemi sırasında dönüştürülür. Her iki durumda da, emisyon oranı muhtemelen burada varsayıldığı gibi hava sınır tabakası üzerinden difüzyon dışında bir süreç tarafından kontrol edilir. Alt komite, bu maruz kalma senaryosunun THPC buharının işlenmiş mobilya döşemesinden THPC buharı emisyonuyla ilişkili THPC buharlarının potansiyel toksisitesi hakkında yararlı bir bilgi sağladığına inanıyor. Bu nedenle, bu yol tarafından THPC'ye maruz kalmanın insanlar için toksik bir risk oluşturup oluşturmadığını belirlemek için daha fazla araştırma yapılmalıdır. Bu sonuçlar, buhar inhalasyon senaryosunun konut ortamında THPC ile işlem gören mobilyalar için gerçekçi olmadığını göstermektedir, çünkü normal koşullar altında tüm THPC'nin buharlaşan kaybı 16 saatte oluşamamıştır. THPC, muamele edilmiş döşeme içinde kimyasal olarak çapraz bağlandığından, THPC'nin buhar basıncı, polimerize form için buhar basıncı olarak kabul edilir. Herhangi bir yayınlanmış veri yokluğunda, THPC'nin polimerize formunun buhar basıncının sıfıra yaklaşacağı varsayılmaktadır. Dolayısıyla, THPC ile işlemden geçirilmiş kumaştan alınan buharı teneffüs etme dışı kanser riski, sıfır olmasa da minimal kabul edilebilir.


AKUT / KRONİK TEHLİKELER

Tetrakis (hidroksimetil) fosfonyum klorür aşındırıcı olabilir. Parçalanmaya kadar ısıtıldığında, POx, hidrojen klorür ve bis (klorometil) eter gibi çok toksik dumanlar yayabilir. Tetrakis (hidroksimetil) fosfonyum kloridin sulu bir ortamda ayrılması fosfin, formaldehit ve hidrojen klorür üretebilir. Tetrakis (hidroksimetil) fosfonyum klorür muhtemelen yanıcıdır.

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