3-Mercaptohexan-1-ol

• Category :

  Organic chemicals and Derivatives/Aroma compounds

• Synonyms :

  1-Hexanol, 3-mercapto-;3-Mercaptohexanol;3-sulfanylhexan-1-ol;(3S)-3-sulfanylhexan-1-ol;(3R)-3-sulfanylhexan-1-ol;3-Mercaptohexan-1-ol;

• CAS NO :

  51755-83-0

• EC NO :

• Molecular Formula :

  C₆H₁₄OS

• Molecular Weight :

  134.2398

• Main Specifications :

  99% min

• InChI :

  InChI=1/C6H14OS/c1-2-3-6(8)4-5-7/h6-8H,2-5H2,1H3/t6-/m1/s1

• Packing :

  25kg，50kg 200kg

• Product description :

  What is the chemical of 3-Mercaptohexan-1-ol? Appearance: colorless to extremely pale clear yellow liquid; Odor: In a 0.10% solution of dipropylene glycol, it presents a sulfur like fruity aroma, which is described as a "tropical rotten fruity aroma ; Assay：99%min by GC ; IR Identity: conform to standard ; HNMR： conform to standard ; carbon spectrum: conform to standard ; Water by K. F.:0.5% max or as per the customer’s request ; Loss on drying:0.5% max. or as per the customer’s request ; boiling point: 250 °C; ============================================================================= purpose 3-mercapto-1-hexanol is mainly used as essence and food additive. It has unique tropical fruit aroma and is often used to prepare edible essence: Food industry: used to prepare flavors such as grapes and eggnog, allowed to be added to baked goods, beverages, candies, dairy products, gummies, etc Daily chemical raw materials: used in personal care products such as perfume and cosmetics to provide fruity keynote 37 Safety certification: Listed as GRAS (Generally Recognized As Safe) by FEMA (Flavor and Extract Manufacturers Association), with FEMA number 3850 and JECFA number 545 ============================================================================ synthetic route 3-mercapto-1-hexanol can be synthesized by the following methods: Chemical synthesis method: 3-sulfohexanol is protected by trimethylsilyl group, brominated with N-bromophthalimide, and then thiolated in one step Biotransformation method: Using oral bacteria to biotransform cysteine S-conjugates, followed by chromatographic purification to obtain

• Uses :

  used as essence and food additive

• Molecular Structure :