1786-08-9 Usage
Description
FEMA 3661, also known as Glycerol, is a polyol compound commonly used as a humectant, solvent, and甜味剂 in various industries. It is found in many natural sources, including apricot, elderberries, grapes, Muscat grapes, Melissa oil, verbena oil, grapefruit juice, passion fruit, cognac, and white wine. Glycerol has a taste threshold value and is characterized by a green, vegetative, floral, leafy, and waxy taste with a herbal and minty depth at 5 ppm.
Uses
Used in Food and Beverage Industry:
FEMA 3661 is used as a humectant, solvent, and甜味剂 to enhance the taste, texture, and shelf life of various food and beverage products.
Used in Pharmaceutical Industry:
FEMA 3661 is used as a solvent and carrier for various pharmaceutical formulations, including liquid medications, tablets, and capsules, to improve their solubility, stability, and bioavailability.
Used in Cosmetics and Personal Care Industry:
FEMA 3661 is used as a humectant and emollient in various cosmetics and personal care products, such as lotions, creams, and shampoos, to provide moisture retention and improve skin hydration.
Used in Oral Care Industry:
FEMA 3661 is used as a humectant and甜味剂 in oral care products, such as toothpaste and mouthwash, to enhance their taste and provide moisture retention for oral health.
Used in Tobacco Industry:
FEMA 3661 is used as a humectant and甜味剂 in various tobacco products, such as e-liquids and moist snuff, to improve their taste and provide moisture retention for a better smoking experience.
Check Digit Verification of cas no
The CAS Registry Mumber 1786-08-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1786-08:
(6*1)+(5*7)+(4*8)+(3*6)+(2*0)+(1*8)=99
99 % 10 = 9
So 1786-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-8(2)6-10-7-9(3)4-5-11-10/h4,6,10H,5,7H2,1-3H3
1786-08-9Relevant articles and documents
Ohloff,Lienhard
, p. 182,185 (1965)
Functionalization of the naturally occurring linalool and nerol by the palladium catalyzed oxidation of their trisubstituted olefinic bonds
Parreira, Luciana A.,Azevedo, Ana F.,Menini, Luciano,Gusevskaya, Elena V.
, p. 429 - 434 (2016/12/16)
Linalool and nerol, bio-renewable terpenic alkenyl alcohols found in many essential oils, were selectively oxidized by molecular oxygen in the presence of the chloride-free Pd(OAc)2/p-benzoquinone catalytic system. An efficient dioxygen-coupled
Process for preparation of nerol oxide
-
Page/Page column 7, (2008/06/13)
The present invention relates to a process for the synthesis of racemic nerol oxide i.e. 3,6-dihydro-4-methyl-2-[2-methyl-1-propenyl)-2H-pyran from monoterpene alcohol nerol i.e. cis-3,7-dimethylocta-2,6-diene-1-ol.
