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Noses

CH2 CH CH0. a colourless, volatile liquid, with characteristic odour. The vapour is poisonous, and intensely irritating to eyes and nose b.p. 53"C. It is prepared by the distillation of a mixture of glycerin, potassium sulphate and potassium hydrogen sulphate. It is manufactured by direct oxidation of propene or cross-condensation of ethanal with meth-anal. [Pg.329]

Nose S 1984 A unified formulation of the constant-temperature molecular dynamics methods J. Chem. Phys. 81 511-19... [Pg.2283]

In practice modifications are made to incorporate thermostats or barostats that may destroy the time-reversible and symplectic properties. While extended-system algorithms such as Nose dynamics [41] can be designed on the principles of the reversible operators, methods that use proportional velocity or coordinate scaling [42] cannot. Such methods arc very... [Pg.6]

Nose, S. A molecular dynamics method for simulations in the canonical ensemble. Mol. Phys. 52 (1984) 255-268 ibid. A unified formulation of the constant temperature molecular dynamics method. J. Chem. Phys. 81 (1984) 511-519. [Pg.30]

CAUTION. Bromine must be handled with great care and in the fume cupboard. The liquid produces painful bums and the vapour is unpleasant. Bromine bums should be treated immediately with a liberal quantity of glycerine. If the vapour is inhaled, relief may be obtained by soaking a handkerchief in alcohol and holding it near the nose. [Pg.278]

The difference m odor between (R) and (S) carvone results from their different behavior toward receptor sites m the nose It is believed that volatile molecules occupy only those odor receptors that have the proper shape to accommodate them Because the receptor sites are themselves chiral one enantiomer may fit one kind of receptor while the other enantiomer fits a different kind An analogy that can be drawn is to hands and gloves Your left hand and your right hand are enantiomers You can place your left hand into a left glove but not into a right one The receptor (the glove) can accommodate one enantiomer of a chiral object (your hand) but not the other... [Pg.295]

At one time thiols were named mercaptans Thus CH3CH2SH was called ethyl mercaptan according to this system This nomenclature was abandoned beginning with the 1965 revision of the lUPAC rules but is still sometimes encountered When one encounters a thiol for the first time especially a low molecular weight thiol its most obvious property is its foul odor Ethanethiol is added to natural gas so that leaks can be detected without special equipment—your nose is so sensitive that it can detect less than one part of ethanethiol m 10 000 000 000 parts of arr The odor of thiols weakens... [Pg.648]

Haworth formulas are satisfactory for representing configurational relationships in pyranose forms but are uninformative as to carbohydrate conformations X ray crystal lographic studies of a large number of carbohydrates reveal that the six membered pyra nose ring of D glucose adopts a chair conformation... [Pg.1038]

Maltose obtained by the hydrolysis of starch and cellobiose by the hydrolysis of cellulose are isomenc disaccharides In both maltose and cellobiose two d glucopyra nose units are joined by a glycosidic bond between C 1 of one unit and C 4 of the other The two are diastereomers differing only m the stereochemistry at the anomeric carbon of the glycoside bond maltose is an a glycoside cellobiose is a (3 glycoside... [Pg.1046]

A particular carbohydrate can mterconvert between furanose and pyra nose forms and between the a and (3 configuration of each form The change from one form to an equilibrium mixture of all the possible hemi acetals causes a change m optical rotation called mutarotation... [Pg.1062]

Potential hydrogen bonding groups (—NH2 and C=0) point away from the fura nose ring... [Pg.1160]

If acetal resins are processed at temperatures substantially above those recommended for the particular grade, minor amounts of formaldehyde may be Hberated. Formaldehyde (qv) is a colorless, lacrimatory gas with a pungent odor and is intensely irritating to mucous membranes. The human nose is sensitive to concentrations in the range of 0.1 to 0.5 ppm. The current threshold limit value for formaldehyde is 1 ppm. [Pg.60]

Acetic anhydride penetrates the skin quickly and painfully forming bums and bUsters that are slow to heal. Anhydride is especially dangerous to the deUcate tissues of the eyes, ears, nose, and mouth. The odor threshold is 0.49 mg/m, but the eyes are affected by as Httie as 0.36 mg/m and electroencephalogram patterns are altered by only 0.18 mg/m. When handling acetic anhydride, mbber gloves that are free of pinholes are recommended for the hands, as well as plastic goggles for the eyes, and face-masks to cover the face and ears. [Pg.79]

Material Safety Data Sheets (MSDS) issued by suppHers of acetone ate requited to be revised within 90 days to include new permissible exposure limits (PEL). Current OSHA PEL (54) and ACGIH threshold limit values (TLV) (55) ate the same, 750 ppm TWA and 1000 ppm STEL. Eot comparison, the ACGIH TWA values for the common mbbing alcohols are ethyl, 1000, and isopropyl, 400 ppm. A report on human experience (56) concluded that exposure to 1000 ppm for an 8-h day produced no effects other than slight, transient irritation of the eyes, nose, and throat. [Pg.98]

With respect to acute toxicity, based on lethaHty in rats or rabbits, acryhc monomers are slightly to moderately toxic. Mucous membranes of the eyes, nose, throat, and gastrointestinal tract are particularly sensitive to irritation. Acrylates can produce a range of eye and skin irritations from slight to corrosive depending on the monomer. [Pg.157]

Full eye protection should be worn whenever handling acryhc monomers contact lenses must never be worn. Prolonged exposure to Hquid or vapor can result in permanent eye damage or blindness. Excessive exposure to vapors causes nose and throat irritation, headaches, nausea, vomiting, and dizziness or drowsiness (solvent narcosis). Overexposure may cause central nervous system depression. Both proper respiratory protection and good ventilation are necessary wherever the possibiHty of high vapor concentration arises. [Pg.157]

The 2-cyanoacryhc esters have sharp, pungent odors and are lacrimators, even at very low concentrations. These esters can be irritating to the nose and throat at concentrations as low as 3 ppm eye irritation is observed at levels of 5 ppm (13). The TLV for methyl 2-cyanoacrylate is 2 ppm and the short-term exposure limit is 4 ppm (14). Good ventilation when using the adhesives is essential. [Pg.178]

The aroma of fmit, the taste of candy, and the texture of bread are examples of flavor perception. In each case, physical and chemical stmctures ia these foods stimulate receptors ia the nose and mouth. Impulses from these receptors are then processed iato perceptions of flavor by the brain. Attention, emotion, memory, cognition, and other brain functions combine with these perceptions to cause behavior, eg, a sense of pleasure, a memory, an idea, a fantasy, a purchase. These are psychological processes and as such have all the complexities of the human mind. Flavor characterization attempts to define what causes flavor and to determine if human response to flavor can be predicted. The ways ia which simple flavor active substances, flavorants, produce perceptions are described both ia terms of the physiology, ie, transduction, and psychophysics, ie, dose-response relationships, of flavor (1,2). Progress has been made ia understanding how perceptions of simple flavorants are processed iato hedonic behavior, ie, degree of liking, or concept formation, eg, crispy or umami (savory) (3,4). However, it is unclear how complex mixtures of flavorants are perceived or what behavior they cause. Flavor characterization involves the chemical measurement of iadividual flavorants and the use of sensory tests to determine their impact on behavior. [Pg.1]

Jiroma. The fragrance or odor of food, perceived by the nose by sniffing. In wines, the aroma refers to odors derived from the variety of grape, eg, muscat aroma. It is the overall odor impression as perceived by the nasal cavity. [Pg.19]

Where surface-active agents are present, the notion of surface tension and the description of the phenomena become more complex. As fluid flows past a circulating drop (bubble), fresh surface is created continuously at the nose of the drop. This fresh surface can have a different concentration of agent, hence a different surface tension, from the surface further downstream that was created earlier. Neither of these values need equal the surface tension developed in a static, equiUbrium situation. A proper description of the flow under these circumstances involves additional dimensionless groups related to the concentrations and diffusivities of the surface-active agents. [Pg.92]

Mild exposure to HF via inhalation can irritate the nose, throat, and respiratory system. The onset of symptoms may be delayed for several hours. Severe exposure via inhalation can cause nose and throat bums, lung inflammation, and pulmonary edema, and can also result in other systemic effects including hypocalcemia (depletion of body calcium levels), which if not promptly treated can be fatal. Permissible air concentrations are (42) OSHA PEL, 3 ppm (2.0 mg/m ) as E OSHA STEL, 6 ppm (5.2 mg/m ) as E and ACGIH TLV, 3 ppm (2.6 mg/m ) as E. Ingestion can cause severe mouth, throat, and stomach bums, and maybe fatal. Hypocalcemia is possible even if exposure consists of small amounts or dilute solutions of HE. [Pg.200]

Formaldehyde causes eye, upper respiratory tract, and skin irritation and is a skin sensitizer. Although sensory irritation, eg, eye irritation, has been reported at concentrations as low as 0.1 ppm in uncontrolled studies, significant eye/nose/throat irritation does not generally occur until concentrations of 1 ppm, based on controlled human chamber studies. Odor detection has commonly been reported to occur in the range of 0.06—0.5 ppm (133—135). [Pg.496]

The development of the principles of nucleation and growth eady in the twentieth century (2) ultimately led to the discovery that certain nucleating agents can induce a glass to crystallize with a fine-grained, highly uniform microstmcture that offers unique physical properties (3). The first commercial glass-ceramic products were missile nose cones and cookware. [Pg.319]


See other pages where Noses is mentioned: [Pg.204]    [Pg.570]    [Pg.99]    [Pg.2996]    [Pg.165]    [Pg.314]    [Pg.317]    [Pg.400]    [Pg.401]    [Pg.717]    [Pg.137]    [Pg.64]    [Pg.1037]    [Pg.1038]    [Pg.1276]    [Pg.688]    [Pg.688]    [Pg.2]    [Pg.70]    [Pg.81]    [Pg.98]    [Pg.186]    [Pg.526]    [Pg.18]    [Pg.1]    [Pg.11]    [Pg.292]   
See also in sourсe #XX -- [ Pg.2 , Pg.52 ]

See also in sourсe #XX -- [ Pg.145 , Pg.181 , Pg.198 ]




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