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  2. Ethylene glycol - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol

    Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol [7]) with the formula (CH 2 OH) 2. It is mainly used for two purposes: as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, flammable, viscous liquid.

  3. Ethane-1,2-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,2-dithiol

    Ethane-1,2-dithiol, also known as EDT, [1] is a colorless liquid with the formula C 2 H 4 2. It has a very characteristic odor which is compared by many people to rotten cabbage . It is a common building block in organic synthesis and an excellent ligand for metal ions.

  4. Ethylene glycol (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol_(data_page)

    720 K (447 °C), 8.2 MPa Standard enthalpy change of fusion, Δ fus H o: 9.9 kJ/mol Standard entropy change of fusion, Δ fus S o: 38.2 J/(mol·K) Standard enthalpy change of vaporization, Δ vap H o: 65.6 kJ/mol Standard entropy change of vaporization, Δ vap S o? J/(mol·K) Solid properties Standard enthalpy change of formation, Δ f H o ...

  5. Ethylene glycol dimethacrylate - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol_dimethacrylate

    Ethylene glycol dimethylacrylate (EGDMA) is a diester formed by condensation of two equivalents of methacrylic acid and one equivalent of ethylene glycol. [2]EGDMA can be used in free radical copolymer crosslinking reactions.

  6. List of UN numbers 1101 to 1200 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_1101_to...

    n.o.s. = not otherwise specified meaning a collective entry to which substances, mixtures, solutions or articles may be assigned if a) they are not mentioned by name in 3.2 Dangerous Goods List AND b) they exhibit chemical, physical and/or dangerous properties corresponding to the Class, classification code, packing group and the name and description of the n.o.s. entry [2]

  7. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    Many syntheses have been developed. One popular route entails reduction of benzoin using zinc amalgam. [6]C 6 H 5 –CH(OH)–C(=O)–C 6 H 5, trans-C 6 H 5 –CH=CH–C 6 H 5. Both isomers of stilbene can be produced by decarboxylation of α-phenylcinnamic acid, trans-stilbene being produced from the (Z)-isomer of the acid.

  8. Pregnancy category - Wikipedia

    en.wikipedia.org/wiki/Pregnancy_category

    Contraindicated in pregnancy: Studies in animals or humans have demonstrated fetal abnormalities and/or there is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience, and the risks involved in use of the drug in pregnant women clearly outweigh potential benefits.

  9. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...