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Methyl 3-methylthiopropionateCAS NO.: 13532-18-8 CAS NO.13532-18-8
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- Product Details
Keywords
- Methyl 3-methylthiopropionate
- 2-Methoxycarbonylethyl methyl sulfide
- 3-Methylbutanethioic S-acid
Quick Details
- ProName: Methyl 3-methylthiopropionateCAS NO.: ...
- CasNo: 13532-18-8
- Molecular Formula: C5H10O2S
- Appearance: powder
- Application: Synthetic fragrances
- DeliveryTime: In stock
- PackAge: drum
- Port: China main port
- ProductionCapacity: 10000 Gram/Day
- Purity: 99%
- Storage: Room temperature
- Transportation: By sea or by air
- LimitNum: 1 Kilogram
- first class: 1-10
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Details
| Description | Methyl 3-Methylthiopropionate is a faint yellow liquid with pineapple organoleptic properties, which belongs to the family of Thia Fatty Acids. It can be isolated from pineapple, melon, naranjila fruit and white wine or obtained by insertion of a sulfur atom at specific positions in the chain. It mostly serves as a flavor and fragrance without safety concern at current levels of intake. Besides, it serves as a additive applied in cigarettes, which was listed in the List of 599 Additives in Cigarettes submitted to the United States Department of Health and Human Services in April 1994. |
| References |
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| Description | Methyl 3-methylthiopropionate has an extremely powerful, penetrating, sweet odor. It is onion-like at high concentrations with a sweet pineapple flavor at high dilutions. Obtained in 84% yields by reacting CH2 = CH — CO — OCH3 with CH3SH; the corresponding acid also has been synthesized. |
| Chemical Properties | Methyl-3-methylthiopropionate has an extremely powerful, penetrating, sweet odor, onion-like at high concentrations and a sweet pineapple flavor at high dilutions. |
| Chemical Properties | CLEAR COLOURLESS LIQUID |
| Occurrence | Reported found in pineapple fruit, white wine, melon and naranjilla fruit. |
| Aroma threshold values | Detection: 180 ppb |
| Taste threshold values | Taste characteristics at 5 ppm: vegetative, radish and horseradish. |
| Chemical Synthesis | Obtained in 84% yields by reacting with CH3SH; the corresponding acid also has been synthesized. |