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acespicoli

Well-known member
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THERE YOU HAVE IT?
🤷‍♂️
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acespicoli

Well-known member
The most purple black stem astringent noxious weed smell the one you will toss cause it smells like some kind of poison...

:yeahthats

In the cure somehow later once the things settle, becomes a incredible musky skunk.
;)
 

pipeline

Cannabotanist
ICMag Donor
Veteran
The promise holds true to numerous combinations of indica and sativa. Have to pheno hunt and develop the line using the plants with the best combination and effect. Select only for resin and less for structure and other traits. Those can be refined in the future.


Sativa Candy Chunk F15

derived from original hybrid in 2010

Sativa Candy Chunk is a mixture of the seed from these 2 lines in the garden in 2010 with pollination by 2 (OG Kush x Jamaican Jam) x DC) x DC males.

(OG Kush x Jamaican Jam) x DC)x DC

Sour Bubble Bx3 x Sour Bubble bx 4 x DC

(Bubba Kush x Bubblegum) x DC) x DC


Sour Bubble Bx3 x Sour Bubble bx 4 x DC
full
 
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acespicoli

Well-known member
Muscone is a macrocyclic ketone, an organic compound that is the primary contributor to the odor of musk. Natural muscone is obtained from musk, a glandular secretion of the musk deer, which has been used in perfumery and medicine for thousands of years. Since obtaining natural musk requires killing the endangered animal, nearly all muscone used in perfumery and for scenting consumer products today is synthetic. It has the characteristic smell of being "musky".

Chemical structure and synthesis​

The chemical structure of muscone was first elucidated by Leopold Ružička. It is a 15-membered ring ketone with one methyl substituent in the 3-position. It is an oily liquid that is found naturally as the (−)-enantiomer, (R)-3-methylcyclopentadecanone. Muscone has been synthesized as the pure (−)-enantiomer as well as the racemate. It is very slightly soluble in water and miscible with alcohol.

One asymmetric synthesis of (−)-muscone begins with commercially available (+)-citronellal, and forms the 15-membered ring via ring-closing metathesis:[1]

Synthesis of muscone via RCM

A more recent enantioselective synthesis involves an intramolecular aldol addition/dehydration reaction of a macrocyclic diketone.[2]


The sweat is oily, cloudy, viscous, and originally odorless;[49] it gains odor upon decomposition by bacteria. Because both apocrine glands and sebaceous glands open into the hair follicle, apocrine sweat is mixed with sebum.[41]
 
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acespicoli

Well-known member
Body odor can smell sweet, sour, tangy or like onions.

What bacteria causes sweat to smell?
The culprit is an enzyme called C-T lyase, found in the bacterium Staphylococcus hominis, which dwells in human armpits. These bacteria feed on odorless chemicals released in sweat, which the enzyme then converts into thioalcohols—a pungent compound responsible for the offending smell.


Another aspect of bacteria is the generation of body odor. Sweat is odorless however several bacteria may consume it and create byproducts which may be considered putrid by humans (as in contrast to flies, for example, that may find them attractive/appealing). Several examples are:


3-Methylbutanoic acid, also known as β-methylbutyric acid or more commonly isovaleric acid, is a branched-chain alkyl carboxylic acid with the chemical formula (CH3)2CHCH2CO2H. It is classified as a short-chain fatty acid. Like other low-molecular-weight carboxylic acids, it has an unpleasant odor. The compound occurs naturally and can be found in many foods, such as cheese, soy milk, and apple juice.

3-Methylbutanoic acid is a minor constituent of the perennial flowering plant valerian (Valeriana officinalis), from which it got its trivial name isovaleric acid: an isomer of valeric acid which shares its unpleasant odor.[2] The dried root of this plant has been used medicinally since antiquity.[3][4] Their chemical identity was first investigated in the 19th century by oxidation of the components of fusel alcohol, which includes the five-carbon amyl alcohols.[5]
 
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