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Isobutyl stearate

Isobutyl stearate structure

Isobutyl stearate 

structure
  • CAS No:

    646-13-9

  • Formula:

    C22H44O2

  • Chemical Name:

    Isobutyl stearate

  • Synonyms:

    Octadecanoic acid,2-methylpropyl ester;Stearic acid,isobutyl ester;Isobutyl stearate;Isobutyl octadecanoate;2-Methylpropyl stearate;Estol 1476;Emerest 2324

  • Categories:

    Cosmetic Ingredient  >  Skin Conditioning

Description

Waxy, crystalline solid.


Liquid

Isobutyl stearate Basic Attributes

340.58

340.58

211-466-1

V8DPR6HNX3

DTXSID9027285

WAX|Paraffin-like, crystal substance @ low temp|Waxy, crystalline solid

2915709000

Characteristics

26.30000

10.09

Liquid

0.8498 g/cm3 @ Temp: 20 °C

28.9 °C

223 °C @ Press: 15 Torr

187.7±8.8 °C

1.447

Very sol in ether

Store below +30°C.

Safety Information

P264, P280, P302+P352, P305+P351+P338, P310, P321, P332+P313, P337+P313, P362

H315

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Not Classified

A skin irritant.

RURAL/REMOTE: Isobutyl stearate was qualitatively detected in a single sample obtained at a countryside apartment in Schmallenberg, Germany, 1988(1).|INDOOR AIR: Isobutyl stearate was qualitatively detected in the emissions from new carpeting(1).

Toxicity

Isobutyl stearate's production and use in cosmetics, inks, coatings, polishes, soaps, and rubber manufacture(1,2) may result in its release to the environment through various waste streams(SRC).

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 33,000(SRC), determined from a structure estimation method(2), indicates that isobutyl stearate is expected to be immobile in soil(SRC). Volatilization of isobutyl stearate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 0.038 atm-cu m/mole(SRC), using a fragment constant estimation method(3). However, adsorption to soil is expected to attenuate volatilization(SRC). Isobutyl stearate is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 2.8X10-5 mm Hg(4). Isobutyl stearate is expected to rapidly biodegrade in aerobic soils as suggested by the rapid biodegradation of structurally similar long-chain fatty acid esters(5-7).|AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 33,000(SRC), determined from a structure estimation method(2), indicates that isobutyl stearate is expected to adsorb to suspended solids and sediment in water(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 0.038 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Volatilization half-lives for a model river and model lake are 5 hours and 7 days, respectively(SRC), using an estimation method(3). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column(SRC). The volatilization half-life from a model pond is estimated to be about 64 hours ignoring adsorption; when considering maximum adsorption the volatilization half-life increases to 10 months(5). According to a classification scheme(6), an estimated BCF of 3(SRC) from an estimated log Kow of 9.63(12) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low. Isobutyl stearate is expected to rapidly biodegrade in aerobic soils as suggested by the rapid biodegradation of structurally similar long-chain fatty acid esters(8-10). An estimated base-catalyzed second-order hydrolysis rate constant of 0.015 L/mole-sec(11,SRC) corresponds to half-lives of 14 and 1.4 years at pH values of 7 and 8, respectively(11).|ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), isobutyl stearate, which has an estimated vapor pressure of 2/8X10-5 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase isobutyl stearate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 15 hours(SRC) from its estimated rate constant of 2.6X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure/reactivity estimation method(3). Particulate-phase isobutyl stearate may be removed from the air by wet and dry deposition(SRC).

The rate constant for the vapor-phase reaction of isobutyl stearate with photochemically-produced hydroxyl radicals has been estimated as 2.6X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure/reactivity estimation method(1). This corresponds to an atmospheric half-life of about 15 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). A base-catalyzed second-order hydrolysis rate constant of 0.016 L/mole-sec(SRC) was estimated using a structure estimation method(2); this corresponds to half-lives of 14 and 1.4 years at pH values of 7 and 8, respectively(2). Isobutyl stearate is not expected to directly photolyze due to the lack of absorption in the environmental UV spectrum.

An estimated BCF of 3 was calculated for isobutyl stearate(SRC) using an estimated log Kow of 9.63(1,SRC) and a regression-derived equation(2). According to a classification scheme(3), the estimated BCF suggests the potential for bioconcentration in aquatic organisms is low.

Using a structure estimation method based on molecular connectivity indices(1), the Koc for isobutyl stearate can be estimated to be about 33,000(SRC). According to a classification scheme(2), this estimated Koc value suggests that isobutyl stearate is expected to be immobile in soil.

The Henry's Law constant for isobutyl stearate is estimated as 0.038 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that isobutyl stearate is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as approximately 5 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as approximately 7 days(SRC). Isobutyl stearate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). The volatilization half-life from a model pond 2 m deep is estimated to be about 64 hours ignoring adsorption; when considering maximum adsorption the volatilization half-life increases to 10 months(3). Isobutyl stearate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). Isobutyl stearate is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 2.8X10-5 mm Hg(4).

NIOSH (NOES Survey 1981-1983) has statistically estimated that 8,524 workers (1,325 of these are female) are potentially exposed to isobutyl stearate in the US(1). Occupational exposure to isobutyl stearate may occur through inhalation and dermal contact with this compound at workplaces where isobutyl stearate is produced or used(SRC). The general population may be exposed to isobutyl stearate due to its presence in cosmetics, inks, coatings, polishes, soaps, and other consumer products(2,3).

Drug Information

/LOW DISSOCIATION CONSTANTS & /...LACK OF WATER SOLUBILITY & ABILITY TO PENETRATE SKIN OR MUCOUS MEMBRANES PROBABLY EXPLAINS THE LACK OF IRRITATION OF HIGHER FATTY ACIDS, THE LIMITED AMT IN SOLN BEING NEUTRALIZED PROMPTLY. /FATTY ACIDS/

Isobutyl stearate Use and Manufacturing

Uses

Waterproof coatings, polishes, face creams, rouges, ointments, soaps, rubber manufacture, dye solutions, inks, lubricants.


Finishing agents


Fabric, textile, and leather products not covered elsewhere

Production

100,000 - 500,000 lb

All other chemical product and preparation manufacturing|Octadecanoic acid, 2-methylpropyl ester: ACTIVE

/METHOD FOR EXTRACTING FATS & FATTY ACIDS AS STEARIC ACID FROM FACE POWDERS BY EXTRACTION & EVAPORATION USING BENZENE & PETROLEUM ETHER AS SOLVENTS. CAUTION: SOLVENTS ARE TOXIC & FLAMMABLE/

Food additives -> Flavoring Agents|Cosmetics -> Emollient; Skin conditioning

Flavoring Agents

Computed Properties

Molecular Weight:340.6
XLogP3:9.9
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:19
Exact Mass:340.334130642
Monoisotopic Mass:340.334130642
Topological Polar Surface Area:26.3
Heavy Atom Count:24
Complexity:261
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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