Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Octyl hydrogen phthalate is a phthalic acid monoester that is obtained through the formal condensation of one of the carboxy groups of phthalic acid with the hydroxy group of octanol. It is characterized by its light brown liquid appearance.

5393-19-1

Post Buying Request

5393-19-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5393-19-1 Usage

Uses

Used in Plastic Industry:
Octyl hydrogen phthalate is used as a plasticizer for enhancing the flexibility, workability, and durability of various types of plastics. Its chemical properties allow it to be easily incorporated into the plastic matrix, resulting in improved performance and reduced brittleness.
Used in Cosmetics and Personal Care Industry:
In the cosmetics and personal care industry, octyl hydrogen phthalate is used as an additive to improve the consistency, texture, and stability of products such as lotions, creams, and nail polishes. Its ability to increase the flexibility and workability of these products makes it a valuable component in the formulation of various cosmetic and personal care items.
Used in Lubricant Industry:
Octyl hydrogen phthalate is utilized as a lubricant additive due to its ability to reduce friction and wear between moving parts. It is particularly useful in the automotive and mechanical industries, where it can be added to lubricants to improve their performance and extend the life of machinery and vehicle components.
Used in Medical Applications:
In the medical field, octyl hydrogen phthalate is used as a component in the production of certain medical devices and equipment. Its properties make it suitable for use in applications where flexibility, durability, and resistance to wear are required, such as in the manufacturing of tubing, catheters, and other medical instruments.
Used in Packaging Industry:
Octyl hydrogen phthalate is employed in the packaging industry as an additive to improve the flexibility and durability of packaging materials. Its incorporation into the packaging materials can enhance their resistance to wear and tear, as well as provide a more appealing and consistent appearance for the products being packaged.

Check Digit Verification of cas no

The CAS Registry Mumber 5393-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5393-19:
(6*5)+(5*3)+(4*9)+(3*3)+(2*1)+(1*9)=101
101 % 10 = 1
So 5393-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O4/c1-2-3-4-5-6-9-12-20-16(19)14-11-8-7-10-13(14)15(17)18/h7-8,10-11H,2-6,9,12H2,1H3,(H,17,18)

5393-19-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Monooctyl Phthalate

1.2 Other means of identification

Product number -
Other names MONOCTYLPHTHALATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5393-19-1 SDS

5393-19-1Synthetic route

phthalic anhydride
85-44-9

phthalic anhydride

octanol
111-87-5

octanol

A

Di-n-octyl phthalate
117-84-0

Di-n-octyl phthalate

B

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

Conditions
ConditionsYield
With montmorillonite K-10 In tetrachloromethane at 76℃; for 12h;A 21%
B 54%
phthalic anhydride
85-44-9

phthalic anhydride

octanol
111-87-5

octanol

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

Conditions
ConditionsYield
at 100 - 110℃;
Heating;
at 105 - 110℃; for 2h;
Di-n-octyl phthalate
117-84-0

Di-n-octyl phthalate

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

Conditions
ConditionsYield
With Tris-HCl buffer; mouse hepatic microsomal esterase ES46.5K In acetone at 37℃; pH=8.0; Enzyme kinetics; Further Variations:; Reagents; Hydrolysis;
phthalic anhydride
85-44-9

phthalic anhydride

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

2-Hydroperoxycarbonyl-benzoic acid octyl ester
139029-99-5

2-Hydroperoxycarbonyl-benzoic acid octyl ester

Conditions
ConditionsYield
With sulfuric acid; dihydrogen peroxide at 10℃; for 1h;66%
vinyl acetate
108-05-4

vinyl acetate

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

phthalic acid octyl ester-vinyl ester
47222-65-1

phthalic acid octyl ester-vinyl ester

Conditions
ConditionsYield
With sulfuric acid; mercury(II) diacetate

5393-19-1Relevant articles and documents

Temperature-resistant salt-tolerant anti-swelling clay stabilizer and synthesis method thereof

-

Paragraph 0026; 0030; 0031; 0037; 0041; 0042; 0048; 0052, (2019/08/28)

The invention belongs to the technical field of oilfield development, and specifically relates to a temperature-resistant and salt-resistant type anti-swelling clay stabilizer and a synthetic method thereof. The temperature-resistant and salt-resistant type anti-swelling clay stabilizer is prepared through the following steps of enabling phthalic anhydride to react with n-octyl alcohol, thus generating n-octyl phthalic anhydride hemi-ester; carrying out a solution polymerization reaction on the n-octyl phthalic anhydride hemi-ester and 2-(dimethylamino) chloromethane hydrochloride, thus generating an intermediate; finally enabling the intermediate to react with benzyl bromide, thus generating the temperature-resistant and salt-resistant type anti-swelling clay stabilizer, wherein a molar ratio of the phthalic anhydride, the n-octyl alcohol, the 2-(dimethylamino) chloromethane hydrochloride and the benzyl bromide is 1 to 1.1 to 1.3 to 1.6. The temperature-resistant and salt-resistant type anti-swelling clay stabilizer disclosed by the invention has the characteristics that the sources of raw materials are wide, a synthetic technology is simple, the dosage is less, and the oil reservoir adaptability is strong; the temperature-resistant and salt-resistant type anti-swelling clay stabilizer is good in temperature resistance and salt resistance, the temperature resistance can reach 250 DEG C, the mineralization resistance degree can reach 200,000 mg/L, and good compatibility is obtained; the temperature-resistant and salt-resistant type anti-swelling clay stabilizer can be forcefully adsorbed to the surface of clay and is not easy to decompose, long in validity period and high in anti-swelling rate, and the anti-swelling rate can reach 98 percent or more.

Ecotoxicity and biodegradation of phthalate monoesters

Scholz, Norbert

, p. 921 - 926 (2007/10/03)

Little is known about the fate and the effects of phthalic acid monoesters. Various of these monoesters ranging from n-butyl to isononyl monoester have been evaluated in respect to their biodegradation behaviour and their acute aquatic toxicity. All esters are readily biodegradable, achieving degradation rates of 90% and more. The acute toxicity values strongly depend on the carbon chain length of the alcohol moiety. The short chain specimen have LC/EC 50 around and above 100 mg/l, with values levelling off to around 30 mg/l for the isononyl monoester.

Adjuvant and immuno-suppressive effect of six monophthalates in a subcutaneous injection model with BALB/c mice

Larsen, Soren Thor,Hansen, Jitka Stilund,Thygesen, Peter,Begtrup, Mikael,Poulsen, Otto Melchior,Nielsen, Gunnar Damgard

, p. 37 - 51 (2007/10/03)

The prevalence of allergic airway diseases is rapidly increasing in Western Europe and North America. This increase in disease prevalence may be associated with environmental pollutants. The present study investigated the adjuvant and immuno-suppressive effect of a series of monophthalates which are considered to be important metabolites of commonly used phthalate plasticizers. The effects were studied in a screening model. Ovalbumin (OA), used as the model antigen, was injected subcutaneously in the neck region of BALB/cJ mice with or without one of the test substances, mono-n-butyl phthalate (MnBP), monobenzyl phthalate (MBnP), mono-n-octyl phthalate (MnOP), mono-2-ethylhexyl phthalate (MEHP), mono-iso-nonyl phthalate (MiNP) or mono-iso-decyl phthalate (MiDP). The levels of OA-specific IgE, IgG1 and IgG2a in sera were measured by ELISA. Immuno-suppressive effect, defined as a statistically significant reduction in IgE or IgG1 antibody production, was observed with MEHP (1000 μg/ml, IgE and IgG1), MnOP (1000 μg/ml, IgE and IgG1), MiNP (1000 μg/ml, IgE and 10 μg/ml, IgG1) and MiDP (100 μg/ml, IgE and IgG1). Adjuvant effect, defined as a statistically significant increase in IgE or IgG1 antibody level, occurred with MEHP (10 μg/ml, IgE), MnOP (100 μg/ml, and 10 μg/ml, IgG1) and MiNP (100 μg/ml, IgE). No statistically significant immune modulating effect was seen with MBnP and MnBP.

Monitoring of phthalic acid monoesters in river water by solid-phase extraction and GC-MS determination

Suzuki,Yaguchi,Suzuki,Suga

, p. 3757 - 3763 (2007/10/03)

An analytical method for monitoring 10 phthalic acid monoesters in river water was investigated by solid-phase extraction, methylation with diazomethane, and GC-MS. Two cartridge-type solid phases packed with octadesyl-coated silica (C18) and styrenedivinyl polymer (PS-2) and one disk-type solid phase made from octadesyl-coated styrene-divinylbenzene polymer (SDB-XD) were investigated in solid-phase extraction. PS-2 gave the highest recoveries of the three solid phases, and recoveries of more than 80% of the monoesters in filtered water samples were obtained at pH 2 to 3 with PS-2 at the spiked level of 0.1 μg L-1, except for monomethyl-phthalate (MMP), in which more than 72% of the monoesters were recovered. For the monoesters in the suspended solids (SS), an acidic methanol extract of SS was added to purified water acidified to pH 2, and the monoesters were extracted with PS-2. The recoveries of the monoesters in SS were more than 80%, but the recoveries of MMP were more than 57%. The method detection limit (MDL) of each phthalic acid monoester in 500 mL of water sample and in 2 mg of dry weight of SS ranged from 0.010 to 0.030 μg L-1 and from 1 to 11 μg g-1 respectively. Monitoring of phthalic acid monoesters in the Tama River in Tokyo was conducted every month from March 1999 to February 2000 using the present method. MMP, mono-n-butyl-phthalate (MBP), and mono-(2-ethylhexyl)-phthalate (MEHP) were detected at concentrations of 0.030-0.0340, 0.010-0.480, and 0.010-1.30 μg L-1. respectively, in the filtered water samples but were not detected in SS. Dimethyl-phthalate (DMP), di-n-butyl-phthalate (DBP), and di-(2-ethylhexyl)-phthalate (DEHP) were detected in the river water at concentrations of 0.010-0.092, 0.008-0.540, and 0.013-3.60 μg L-1, respectively. Diethyl-, di-iso-butyl-, and benzylbutyl-phthalates were also detected at concentrations of nanograms per liter, whereas the corresponding monoesters did not appear. The concentrations of MBP and MEHP in the river water were slightly lower than those of the corresponding diesters at the majority of sampling sites and sampling times.

Montmorillonite clay catalysis. Part 10. K-10 and KSF-catalysed acylation of alcohols, phenols, thiols and amines: Scope and limitation

Li, Tong-Shuang,Li, Ai-Xiao

, p. 1913 - 1917 (2007/10/03)

Montmorillonite K-10 and KSF are highly efficient catalysts for the acetylation of a variety of alcohols, thiols, phenols and amines with acetic anhydride. Amino groups can be selectively acetylated in the presence of hydroxy groups, while the hydroxy groups can be preferentially acetylated in the presence of thiol groups. No selectivity is observed between primary and secondary hydroxy groups in the presence of K-10 and KSF. The catalysts are found not to be efficient for acetylation of tertiary alcohols. This method is simple and convenient with minimum environmental impact. The catalysts are also effective for the acylation of alcohols, thiols, phenols and amines with acetyl chloride and benzoyl chloride. Cyclic anhydrides such as succinic anhydride, maleic anhydride and phthalic anhydride and p-toluene sulfonyl chloride show less reactivity than acetic anhydride and acyl chlorides.

Involvement of a novel mouse hepatic microsomal esterase, ES46.5K, in the hydrolysis of phthalate esters

Kayano, Yuichiro,Watanabe, Kazuhito,Matsunaga, Tamihide,Yamamoto, Ikuo,Yoshimura, Hidetoshi

, p. 749 - 751 (2007/10/03)

ES46.5K, a novel esterase from mouse hepatic microsomes (Watanabe K., et al., Biochem. Mol. Biol. Int., 31, 25-30 (1993)), catalyzed hydrolysis of phthalate esters. ES46.5K and mouse hepatic microsomes hydrolyzed diethyl-, dibutyl-, diisobutyl-, dioctyl- and diethylhexyl phthalates, whereas dicyclohexyl- and dipbenyl phthalates having ring structure were not hydrolyzed by the enzymes. V(max) (μmol/min/mg protein)/K(m) (μM) ratios of ES46.5K for diethyl-, dibutyl-, diisobutyl-, dioctyl- and diethylhexyl phthalates were 291, 2786, 565, 51 and 57, respectively, while those of microsomes were 0.58, 0.83, 1.71, 0.05 and 1.10, respectively. The hydrolytic activity of ES46.5K was inhibited by diisopropylfluorophosphate and bis-p- nitrophenylphosphate. These results suggest that ES46.5K has high catalytic activity for phthalate esters and some role in the metabolism of phthalate esters in mice.

NOUVEAUX DECONTAMINANTS. ACTION DES PERACIDES A GROUPE ESTER SUR QUELQUES TOXIQUES INSECTICIDES OU DE GUERRE

Lion, C.,Hedayatullah, M.,Bauer, P.,Boukou-Poba, J. P.,Charvy, C.,et al.

, p. 555 - 560 (2007/10/02)

A new peroxyacid-ester series has been obtained and used in the destruction of toxic agents.These structures oROCOC6H4CO3H and ROCO(CH2)nCO3H are more stable than the unsubstituted compounds.The reaction with paraoxon (O,O-diethyl O-paranitrophenylphosphate) and HD (2,2'-dichlorodiethylsulfide) goes to completion in a very short time.The influence of the R group and the length of the chain (n=2......12) has been studied.The addition of some long chain tetraalkyl-ammonium salts enhances the rate of the reaction by micellar catalysis.

Process for producing benzene carboxylic acid ester

-

, (2008/06/13)

Benzenecarboxylic acid ester is produced at a higher reaction rate in a better yield in a shorter time by reacting benzenecarboxylic acid having 8 to 10 carbon atoms or its anhydride with aliphatic alcohol having 7 to 11 carbon atoms in the presence of amorphous aluminum compound as a catalyst and an alkali metal compound as a promoter.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5393-19-1