630-06-8CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCYDLYQMBWCWFRAI-UHFFFAOYSA-NHexatriacontane is an alkane that has 36 carbons and a straight-chain structure.
630-06-8DTXSID7060885CHEBI:72688Other Classes -> Aliphatics, Saturated (>C11)
n-Alkane
White, translucent solid; tasteless; odorless; consisting of a mixture of solid hydrocarbons of high molecular weight e.g. C36H74; Soluble in benzene, ligroin, warm alcohol, chloroform, turpentine, carbon disulfide, and olive oil; Insoluble in water and acids; combustible /Paraffin Wax/
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
This chemical does not meet GHS hazard criteria for 100% (44 of 44) of all reports.
Not Classified
Aggregated GHS information provided per 44 reports by companies from 1 notifications to the ECHA C&L Inventory.
Wear self contained breathing apparatus for fire fighting if necessary.
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
They are used mainly in applications for which isoalkanes are not acceptable for biological reasons, e.g., the production of detergents or proteins. /Higher n-Alkanes/
Solid n-alkanes (paraffin waxes) are used in a variety of applications, e.g., ... oxidation, and chlorination reactions. /Higher n-Alkanes/
The liquefaction of coal provides the greatest variety of saturated hydrocarbons. The Fischer-Tropsch synthesis produces alkanes from syngas (CO + H2) in the range C1 to C30 or higher depending on the process variant: depending on the catalyst employed, the synthesis yields predominantly liquid hydrocarbons in the gasoline range, along with gases from C1 to C4 when iron-based catalysts are used, while cobalt-based catalysts produce longer chain hydrocarbons in the diesel and wax range that often undergo, depending of the desired product slate, further processing, especially for gasoline generation. While iron-based Fischer-Tropsch catalysts generate complex mixtures that also include branched and olefinic hydrocarbons, cobalt-based catalysts produce streams that are rich in n-alkanes and are therefore suitable raw materials for detergents and for wax products. /Saturated Hydrocarbons/
Suitable sources for n-alkanes with more than six carbon atoms are the appropriate petroleum distillate fractions, from which the n-paraffins can be isolated in high isomeric purity (= 95% linearity) by selective separation techniques, especially fractional distillation. /Higher n-Alkanes/
Hexatriacontane: ACTIVE
Gas-phase dehydrogenation of n-alkanes over noble-metal catalysts yield the corresponding n-alkenes at low conversion rates (ca. 10%) with predominantly internal double bonds. The corresponding alkenes can be isolated in high purity by selective molecular-sieve processes. /Higher n-Alkanes/
용도Hexatriacontane is a monomer of poly cyclic aromatic hydrocarbons that are found in wetlands.
일반 설명1-Hexene can undergo bio-oxidation to form 5-hexen-1-ol, which can undergo further oxidation to yield 5-hexenoic acid. It can also find applications as a comonomer in the production of polyethylene.
현재 필터 조건에 해당하는 반응 기록이 없습니다.
불러오는 중…
white shiny flakes
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Avoid dust formation. Avoid breathing vapors, mist or gas. Environmental precautions: Do not let product enter drains. Methods and materials for containment and cleaning up: Sweep up and shovel. Keep in suitable, closed containers for disposal.
SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
Product: Offer surplus and non-recyclable solutions to a licensed disposal company. Contaminated packaging: Dispose of as unused product.
Provide appropriate exhaust ventilation at places where dust is formed. Normal measures for preventive fire protection.
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Avoid dust formation. Avoid breathing vapors, mist or gas. Environmental precautions: Do not let product enter drains. Methods and materials for containment and cleaning up: Sweep up and shovel. Keep in suitable, closed containers for disposal.
Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.
SRP: Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area. Ventilation control of the contaminant as close to its point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants. Ensure that the local ventilation moves the contaminant away from the worker.
SRP: The scientific literature for the use of contact lenses by industrial workers is inconsistent. The benefits or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
Eye/face protection: Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection: Handle with gloves.
Body Protection: Choose body protection in relation to its type, to the concentration and amount of dangerous substances, and to the specific work-place.
Respiratory protection: Respiratory protection is not required. Where protection from nuisance levels of dusts are desired, use type N95 (US) or type P1 (EN 143) dust masks. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 8.7X10+9(SRC), determined from a structure estimation method(2), indicates that hexatricontane is expected to be immobile in soil(SRC). Volatilization of hexatricontane from moist soil surfaces is expected to be a fate process(SRC) given an estimated Henry's Law constant of 8400 atm-cu m/mole(SRC), using a fragment constant estimation method(2). However, adsorption to soil is expected to attenuate volatilization(SRC). Hexatricontane is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 9.2X10-9 mm Hg at 25 °C(SRC), determined from a fragment constant method(2). A biodegradation oxygen consumption value of 7.6 ug/mL using a soil suspension(3) indicates that biodegradation of hexatriacontane may be a slow environmental fate process in soil(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 8.7X10+9(SRC), determined from a structure estimation method(2), indicates that hexatriacontane is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 8400 atm-cu m/mole(SRC), developed using a fragment constant estimation method(1). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 6.6 and 210 hours, respectively(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is more than 2 years if adsorption is considered(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from an estimated log Kow of 18.02(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). A biodegradation oxygen consumption value of 7.6 ug/mL using a soil suspension(3) indicates that biodegradation of hexatriacontane may be a slow environmental fate process in water(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), hexatriacontane, which has an estimated vapor pressure of 9.2X10-09 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase hexatriacontane may be removed from the air by wet and dry deposition(SRC). Hexatriacontane does not contain chromophores that absorb at wavelengths >290 nm(3) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).
Hexatriacontane detections in plants used in food and medicinal applications(1). /Hexatriacontaine/[Table#8392]
n-Hexatriacontane detections in plants used in food and medicinal applications(1).[Table#8393]
Using a structure estimation method based on molecular connectivity indices(1), the Koc of hexatriacontane can be estimated to be 8.7X10+9 (SRC). According to a classification scheme(2), this estimated Koc value suggests that hexatriacontane is expected to be immobile in soil.
URBAN/SUBURBAN: A mean hexatriacontane concentration of approximately 1 ng/cu m was reported in the particulate phase of air samples collected in an urban and industrialized area in Prato, Italy during 2002(1). Hexatriacontane concentrations were 2.8 and 2.0 ng/cu m in particulate phase in the summer and winter, respectively, and 0.2 ng/m3 in vapor phase in both summer and winter; samples were collected in an urban area in Nagoya, Japan in 1991(2).
AEROBIC: Oxygen consumption of 7.6 ug/mL over 10 days was reported for hexatriacontane using a soil suspension of Hudson-Collamer silt loam soil incubated in the dark at 25 °C(1).
PURE CULTURE: Using 5 different marine bacterial strains and 4 different nitrogen sources, biodegradation of petroleum oil was examined under aerobic conditions at 26 °C for 10 days. Data reported for hexacosane (C26), octacosane (C28), and triacontane (C30), which were present as components of the petroleum oil, indicatd that these compounds were degraded by 4 of 5 bacterial strains with certain nitrogen sources and consumption ranged from 5 to 96%(1). Other long chain alkanes like hexatriacontane (C36) may behave similarly(SRC).
An estimated BCF of 3 was calculated in fish for hexatriacontane(SRC), using an estimated log Kow of 18.02(1) and a regression-derived equation(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Henry's Law constant for hexatriacontane is estimated as 8400 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that hexatriacontane is expected to volatilize 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 6.6 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 9 days(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is greater than 2 years when adsorption is considered(3). Hexatriacontane's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Hexatriacontane is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 9.2X10-9 mm Hg(SRC), determined from a fragment constant method(1).
Hexatriacontane is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(1). Hexatriacontane does not contain chromophores that absorb at wavelengths >290 nm(1) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).
According to the 2012 TSCA Inventory Update Reporting data, there are 0 reporting facilities for hexatriacontane(1).
Occupational exposure may be through inhalation and dermal contact with hexatricontane at workplaces where coal and petroleum derived substances are produced or used or where combustion processes are extensive. The general population may be exposed to hexatriacontane through inhalation of polluted air, ingestion of food and contact with water contaminated by combustion effluents. (SRC)
정의ChEBI: An alkane that has 36 carbons and a straight-chain structure.