1. Butanethiol is a thiol of low molecular weight, and it is highly flammable.

2. The sulfur atoms of the thiol groups are the site of interaction with arsenic.

3. The reactivity of perbenzoylated thioglycosides with various thiol aglycons has been compared and quantified using competitive glycosylation experiments.

4. Prior to erythrocyte sensitization, the Agglutinator site on Fab fragments can be blocked by thiol-disulfide exchange

5. Many of these schemes use a covalent attachment scheme, using oligonucleotides with amide or thiol functional groups as a chemical handle to bind the heteroelements.

6. Conjugates prepared with the thiol-reactive Alkyne, succinimidyl ester can be detected with an azide-containing molecule in a click chemistry reaction

7. In addition, the zinc sulfide nanoparticles having a thiol protective surface can endure the formation temperature of a thermoplastic polymer resin matrix.

8. alkyl, and the weight ratio of chloro acetanilide derivatives of general formula (I) to the thiol carbamate derivatives of general formula (II) is 1.2-1:3-1.

9. Aqueous formulations of ciliary neurotrophic factor (CNTF) suitable for lyophilization and subsequent reconstitution in which rhCNTF is admixed with a bulking agent and a thiol-containing antioxidant are provided.

10. The starting material 5-amino-1, 3, 4-thiadiazole-2-thiol and followed by a series of 5-fatty-Acylamido-1, 3, 4-thiadiazole-2-thiols (4a–4j) were synthesized with different fatty acid chlorides

11. The free thiol compound and reducing agent can be added during milling, dry mix, wet mix, or other admix, so that the agents are present throughout the food product.

12. Thiol-SAMMS can also recover precious metals such as copper and gold, and researchers are now switching out the sulfur for other atoms so that it could mop up radioactive waste.

13. The invention relates to liquid thermally hardening mixtures comprising: A) low-molecular weight polyols with at least three hydroxyl groups and a hydroxy group content corresponding to a theoretical OH-number of 800 to 1,900 mg KOH/g, B) compounds selected from the group of cyclic and acyclic C9 - C16 alkanes, functionalised with hydroxy groups or hydroxy groups and at least one thiol group and C) low molecular weight or oligomeric compounds with reactive functional groups (c1) complementary to hydroxy and thiol groups, methods for production and use thereof.

14. Thiol 1a is stable at acidic pH, but is unstable at pH 7.8, Cyclizes and loses NH3 to give N-TP1-2-iminothiolane (3a), ES-MS (m/z) [602.1 (M+H)(+)], as well as regenerating TP1

15. The present invention relates to a curable adhesive composition comprising a first part and a second part, the curable adhesive composition comprising: in the first part at least one epoxy resin and in the second part at least one curing agent in the form of an epoxy-amine and/or epoxy-thiol adduct obtainable by reacting at least one primary amine, secondary amine and/or a thiol with at least one polyol compound comprising at least one terminal epoxy group.

16. Carboxyl groups present on the surface of CNTs are often employed for the attachment of amine-terminated or mercapto-terminated nMO via amide bonds achieved by direct conjugating mercapto-terminated or amine-terminated nanoparticles with Carboxylated CNTs or after converting Carboxyl groups into thiol groups to anchor colloidal nanoparticles [27].

17. Commission Implementing Regulation (EU) 2018/250 of 15 February 2018 concerning the authorisation of methyl 2-furoate, bis-(2-methyl-3-furyl) disulfide, furfural, furfuryl alcohol, 2-furanmethanethiol, S-furfuryl acetothioate, difurfuryl disulfide, methyl furfuryl sulfide, 2-methylfuran-3-thiol, methyl furfuryl disulfide, methyl 2-methyl-3-furyl disulfide and furfuryl acetate as feed additives for all animal species ( 1 )

18. Inositol derivatives are described that are represented by the structural formula (I) wherein X is a radical of scyllo-inositol wherein one or more of R1, R2, R3, R4, R5, and R6 are independently alkyl, alkenyl, alkynyl, alkylene, alkenylene, alkoxy, alkenyloxy, cycloalkyl, cycloalkenyl, cycloalkoxy, aryl, aryloxy, arylalkoxy, aroyl, heteroaryl, heterocyclic, acyl, acyloxy, sulfoxide, sulfate, sulfonyl, sulfenyl, sulfonate, sulfinyl, amino, imino, azido, thiol, thioalkyl, thioalkoxy, thioaryl, nitro, cyano, halo, seleno, silyl, silyloxy, silylthio, carboxyl, carbonyl, carbamoyl, or carboxamide and the other of R1, R2, R3, R4, R5, or R6 are hydroxyl, or pharmaceutically acceptable salts thereof.