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Search results for benzyl root_names_name in Any Name (approximate match)
Status:
Possibly Marketed Outside US
Source:
21 CFR 333D
(2012)
Source URL:
First approved in 1996
Source:
NDA020538
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Oleyl alcohol (also octadecenol or cis-9-octadecen-1-ol) is a non-ionic, unsaturated fatty alcohol. Oleyl alcohol is a long-chain aliphatic alcohol that occurs naturally in fish oils. It is used in such large-scale applications as the softening and lubrication of textile fabrics, and the production of carbon paper, stencil paper, and printing ink. Oleyl alcohol is also utilized as an antifoam agent and cutting lubricant. It also is a precursor for the preparation of its sulfuric ester derivatives, which are used in detergents and wetting agents. Oleyl alcohol has been incorporated into various formulations for drug delivery. Oleyl alcohol is found in a wide variety of products such as hair conditioners, foundations, eye makeup, skin moisturizers, skin cleansers and other skin care products. Oleyl alcohol helps to form emulsions and prevents an emulsion from separating into its oil and liquid components. It also reduces the tendency of finished products to generate foam when shaken. When used in the formulation of skin care products, Oleyl alcohol acts as a lubricant on the skin surface, which gives the skin a soft, smooth appearance.
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2011)
Source URL:
First approved in 1995
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
KLEER-PLEX ADVANCED ACNE CARE SYSTEM
Source URL:
First approved in 1994
Source:
ANDA077538
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Phenethyl alcohol, or 2-phenylethanol, is an aromatic alcohol with a rosy scent. It is widely used in the food, fragrance, and cosmetic industries. It is used in the formulation of eye area makeup, skin care products, shampoos, perfumes, and colognes. Promising sources of natural 2-phenylethanol are microorganisms, especially yeasts, which can produce it by biosynthesis and biotransformation.
Status:
Possibly Marketed Outside US
Source:
M016
(2023)
Source URL:
First approved in 1990
Source:
M032
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Targets:
Conditions:
Linalool (3,7-dimethyl-1,6-octadien-3-ol) is a very fragrant component of various herbs such as lavender, mint, and coriander that can be a potent skin irritant, causing contact dermatitis in some sensitive individuals. Linalool is used as a scent in perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions. Linalool is used by pest professionals as a flea, fruit fly, and cockroach insecticide. It can also be used a method of pest control for codling moths. Linalool creates a synergistic effect with the codling moth's pheromone called codlemone, which increases the attraction of males. Linalool can be absorbed by inhalation of its aerosol and by oral intake or skin absorption, potentially causing irritation, pain and allergic reactions.
Status:
Possibly Marketed Outside US
Source:
NDA019822
(1989)
Source URL:
First approved in 1989
Source:
NDA019822
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
21 CFR 358H
(2017)
Source URL:
First approved in 1988
Source:
NDA019452
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
OLETH-2 is a polyethylene glycol ether of Oleyl Alcohol. The number in the name is the average number of ethylene oxide units. OLETH-2 ethoxylated alcohol is derived from a vegetable based alcohol. It is an easy-to-use liquid form. OLETH-2 ethoxylated alcohol is an exceptional nonionic water in oil emulsifier and is recommended for a wide range of topical product and applications. In cosmetics and personal care products, the Oleth ingredients are used in the formulation of skin care products, makeup and hair care products.
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2010)
Source URL:
First approved in 1984
Source:
ANDA209351
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
21 CFR 333C
(2014)
Source URL:
First approved in 1984
Source:
ANDA209351
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
ISOAMYL ACETATE is an organic compound that is the ester formed from isoamyl alcohol and acetic acid. It is present in many fruit aromas, especially banana, and is used in banana flavoring. It is a clear colorless liquid that is only slightly soluble in water, but very soluble in most organic solvents.
Status:
Possibly Marketed Outside US
Source:
ANDA083231
(1973)
Source URL:
First approved in 1973
Source:
ANDA083231
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Benzyl chloride, or α-chlorotoluene, is a reactive organochlorine compound that is a widely used chemical building block. Industrially, benzyl chloride is the precursor to benzyl esters which are used as plasticizers, flavorants, and perfumes. Phenylacetic acid, a precursor to pharmaceuticals, is produced from benzyl cyanide, which is generated by treatment of benzyl chloride with sodium cyanide. Quaternary ammonium salts, used as surfactants, are readily formed by alkylation of tertiary amines with benzyl chloride. Benzyl chloride is an alkylating agent with very irritating properties to the skin. Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare.
Status:
Possibly Marketed Outside US
Source:
21 CFR 333D
(2011)
Source URL:
First approved in 1972
Source:
21 CFR 333A
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Tert-Butyl alcohol (TBA), also called tert-butanol, an important intermediate in industrial chemical synthesis, is poorly absorbed through skin, but is rapidly absorbed upon inhalation or ingestion and distributed to tissues throughout the body. There is no much information related to the toxicity and pharmacological properties of tert-butanol in humans and animals. However, the recently published article has shown that TBA-associated non-neoplastic and neoplastic histopathological changes in the rat's kidney could be explained by alpha2u-globulin nephropathy (α2u-gN) or enhanced chronic progressive nephropathy (CPN), neither of which are relevant to humans.