Çâ±â¹°Áú : Damascenone, Àå¹Ì, ¸ÆÁÖ, ¿ÍÀÎ


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Çâ±â¹°Áú  : Damascenone

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- Àå¹ÌÀ̾߱â, Àå¹Ì¿ÀÀÏ

- ¸ÆÁÖ, ¿ÍÀÎ
- ¼ö¹Ú, Å丶Åä



Damascenone ´Â Àå¹Ì(Rosa damascene) À̸§¿¡¼­ À¯·¡Çß´Ù.  50³âÀü Kováts´Â ºÒ°¡¸®¾ÆÀÇ Àå¹Ì¿ÀÀÏÀ» ºÐ¼®ÇÏ¿© ÀÌ°ÍÀÌ ÁÖ Çâ±â¹°ÁúÀÓÀ» ¹àÇû´Ù.
Beta-DamascenoneÀº ¸Å¿ì ÀÛÀº ¾çÀ¸·Î °¨Áö °¡´ÉÇÏ´Ù. Àå¹Ì¿ÀÀÏ¿¡¼­ ÇÔ·®Àº ½ÃÆ®·Î³Ú·Ñ(38%)ÀÇ 1/270ÀÌÁö¸¸ 1/4400ÀÇ ÀÛÀº ¾çÀ¸·Î °¨°¢ÀÌ °¡´ÉÇØ Àå¹ÌÇâ¿¡ ±â¿©µµ°¡ 16¹è³ª ³ô´Ù.
¾ËÄڿðú È¥ÇÕ¹°¿¡¼­´Â 1000¹è³ª Àß °¨ÁöµÇ¾î ¸ÆÁÖ¿Í ¿ÍÀο¡¼­ °¡Àå Áß¿äÇÑ Çâ±â¹°Áú ÁßÀÇ ÇϳªÀÌ´Ù
¿ÍÀο¡¼­ ethyl esters (ethyl cinnamate and ethyl hexanoate)ÀÇ ÇâÀ» »ó½Â½ÃÄÑ °úÀÏÇâÀ» °­È­ÇÏ°í, ½ÃÅ°°í 3-isobutyl-2-methoxypyrazineÇâÀ» °¨¼Ò½ÃÄÑ Çãºê/ä¼ÒÀÇ ´À³¦À» ¸¶½ºÅ·ÇÑ´Ù. ¿ÍÀÎÇâ¿¡ °£Á¢ÀûÀÎ ¿µÇâÀÌ ´õ Å« °ÍÀÌ´Ù

Damascenone takes its name from Rosa damascena, the Damask rose, which does take its name from Damascus – this cultivated rose is believed to originate in the Near East, maybe having been brought back from there at the time of the Crusades. In any case, it is an easier name to remember than 3,5,8-Megastigmatrien-7-one, let alone 1-(2,6,6-Trimethyl-1,3-cyclohexadien-1-yl)-2-buten-1-one.

Some 50 years ago, Kováts, working at ETH Zurich, analysed Bulgarian rose oil (from Rosa damascena), identifying a wide range of molecules present, some in large amounts, some in tiny quantities. However, to adapt an expression of George Orwell¡¯s (Animal Farm), ¡°All molecules are equal, but some are more equal than others¡±. It is some of the least abundant molecules which have the greatest influence on the smell of roses, as they are molecules which individually have a very intense smell.
A molecule like citronellol makes up over 1/3 of the rose oil studied, but its odour threshold, the level below which it cannot be detected by nose, is quite high (40 parts per billion). Thus molecules like that make a small contribution to the smell of rose oil.

Damascenone, a C-13 norisoprenoid, is an important aroma compound and is universally found in grapes and nearly all wines. It was first characterized as a rose ketone compound1 and has since been described as contributing aromas of honey, fruit, floral, tea, stewed apple, dry plum, dark berries and caramel2-4. In a wine matrix, the odor threshold for damascenone is 4-7 ¥ìg/L5. Damascenone is typically found at levels below this threshold in red wines (1-2 ¥ìg/L) and at or above this level in white wines (5-10 ¥ìg/L). Literature suggests damascenone has an indirect impact on red wine aroma. Damascenone has been shown to increase the threshold of fruity esters (ethyl cinnamate and ethyl caproate) and decrease the odor threshold for IBMP, green bell pepper