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List Of UN Numbers 2101 To 2200
UN numbers from UN2101 to UN2200 as assigned by the United Nations Committee of Experts on the Transport of Dangerous Goods are as follows: __NOTOC__ UN 2101 to UN 2200 See also *Lists of UN numbers References External linksADR Dangerous Goods cited on 7 May 2015.UN Dangerous Goods List from 2015 cited on 7 May 2015.UN Dangerous Goods List from 2013 cited on 7 May 2015. {{UN number list navbox Lists of UN numbers ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tert-Butyl Peroxymaleate
In organic chemistry, butyl is a four-carbon alkyl radical (chemistry), radical or moiety (chemistry), substituent group with general chemical formula , derived from either of the two isomers (''n''-butane and isobutane) of butane. The isomer ''n''-butane can connect in two ways, giving rise to two "-butyl" groups: * If it connects at one of the two terminal carbon atoms, it is normal butyl or ''n''-butyl: (preferred IUPAC name: butyl) * If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or ''sec''-butyl: (preferred IUPAC name: butan-2-yl) The second isomer of butane, isobutane, can also connect in two ways, giving rise to two additional groups: * If it connects at one of the three terminal carbons, it is isobutyl: (preferred IUPAC name: 2-methylpropyl) * If it connects at the central carbon, it is tertiary butyl, ''tert''-butyl or ''t''-butyl: (preferred IUPAC name: ''tert''-butyl) Nomenclature According to IUPAC nomenclature, "iso ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Peroxyacetic Acid
Peracetic acid (also known as peroxyacetic acid, or PAA) is an organic compound with the formula CH3CO3H. This peroxy acid is a colorless liquid with a characteristic acrid odor reminiscent of acetic acid. It can be highly corrosive. Peracetic acid is a weaker acid than the parent acetic acid, with a p''K''a of 8.2. Production Peracetic acid is produced industrially by the autoxidation of acetaldehyde: :O2 + CH3CHO → CH3CO3H It forms upon treatment of acetic acid with hydrogen peroxide with a strong acid catalyst: :H2O2 + CH3CO2H CH3CO3H + H2O As an alternative, acetyl chloride and acetic anhydride can be used to generate a solution of the acid with lower water content. Peracetic acid is generated ''in situ'' by some laundry detergents. This is achieved by the action of bleach activators, such as tetraacetylethylenediamine and sodium nonanoyloxybenzenesulfonate, upon hydrogen peroxide formed from sodium percarbonate in water. The peracetic acid is a more effective blea ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Di-(3,5,5-trimethylhexanoyl)peroxide
Numeral or number prefixes are prefixes derived from numerals or occasionally other numbers. In English and many other languages, they are used to coin numerous series of words. For example: * unicycle, bicycle, tricycle (1-cycle, 2-cycle, 3-cycle) * dyad, triad (2 parts, 3 parts) * biped, quadruped (2 legs, 4 legs) * September, October, November, December (month 7, month 8, month 9, month 10) * decimal, hexadecimal (base-10, base-16) * septuagenarian, octogenarian (70-79 years old, 80-89 years old) * centipede, millipede (around 100 legs, around 1000 legs) In many European languages there are two principal systems, taken from Latin and Greek, each with several subsystems; in addition, Sanskrit occupies a marginal position. There is also an international set of metric prefixes, which are used in the metric system and which for the most part are either distorted from the forms below or not based on actual number words. Table of number prefixes in English In the following pr ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ethyl Methyl Ketone Peroxide
Methyl ethyl ketone peroxide (MEKP) is an organic peroxide with the formula CH3)(C2H5)C(O2H)sub>2O2. MEKP is a colorless oily liquid. It is widely used in vulcanization (crosslinking) of polymers. It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide. Several products result from this reaction including a cyclic dimer. The linear dimer, the topic of this article, is the most prevalent. and this is the form that is typically quoted in the commercially available material. Solutions of 30 to 40% MEKP are used in industry and by hobbyists as catalyst to initiate the crosslinking of unsaturated polyester resins used in fiberglass, and casting. For this application, MEKP often is dissolved in a phlegmatizer such as dimethyl phthalate, cyclohexane peroxide, or diallyl phthalate to reduce sensitivity to shock. Benzoyl peroxide can be used for the same purpose. Safety Whereas acetone peroxide is a white powder at STP, MEKP is slightly less sensitive to shock a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Methyl Isobutyl Ketone Peroxide
In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula . In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in most molecules. While the methyl group is usually part of a larger molecule, bounded to the rest of the molecule by a single covalent bond (), it can be found on its own in any of three forms: methanide anion (), methylium cation () or methyl radical (). The anion has eight valence electrons, the radical seven and the cation six. All three forms are highly reactive and rarely observed. Methyl cation, anion, and radical Methyl cation The methylium cation () exists in the gas phase, but is otherwise not encountered. Some compounds are considered to be sources of the cation, and this simplification is used pervasively in organic chemistry. For example, protonation of methanol gives an electr ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
P-Menthane Hydroperoxide
''p''-Menthane is a hydrocarbon with the formula (CH3)2CHC6H10CH3. It is the product of the hydrogenation or hydrogenolysis of various terpenoids, including ''p''-cymene, terpinolenes, phellandrene, and limonene. It is a colorless liquid with a fragrant fennel-like odor. It occurs naturally, especially in exudates of ''Eucalyptus'' fruits. The compound is generally encountered as a mixture of the ''cis'' and ''trans'' isomers, which have very similar properties. It is mainly used as a precursor to its hydroperoxide, which is used to initiate polymerization In polymer chemistry, polymerization (American English), or polymerisation (British English), is a process of reacting monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks. There are many fo ...s. References {{DEFAULTSORT:Menthane, p- Hydrocarbons Perfume ingredients Cyclohexanes Isopropyl compounds ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dilauroyl Peroxide
Dilauroyl peroxide is an organic compound with the formula (C11H23CO2)2. A colorless solid, it is often sold as a water-damped solid. It is the symmetrical peroxide of lauric acid. It is produced by treating lauroyl chloride Lauroyl chloride is the organic compound with the formula CH3(CH2)10COCl. It is the acid chloride of lauric acid. Lauroyl chloride is a standard reagent for installing the lauroyl group. It is mainly produced as a precursor to dilauroyl peroxid ... with hydrogen peroxide in the presence of base: :2C11H23COCl + H2O2 + 2NaOH → (C11H23CO2)2 + 2{{nbspHCl References Organic peroxides Radical initiators ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
