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Search results for benzyl root_references_citation in Reference Text / Citation (approximate match)
Status:
Possibly Marketed Outside US
Source:
M020
(2024)
Source URL:
First approved in 2003
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
Phos-Aid by Butler Animal Health Supply LLC
(2000)
Source URL:
First approved in 2000
Source:
Phos-Aid by Butler Animal Health Supply LLC
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Status:
Possibly Marketed Outside US
Source:
Clearasil
Source URL:
First approved in 1999
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Status:
Possibly Marketed Outside US
Source:
M020
(1997)
Source URL:
First approved in 1997
Source:
M020
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Myristyl Alcohol is a fatty alcohol used as an emollient in cosmetics and skin care products also serve as a basic component and solubility aid in metalworking fluids. Contact sensitization to myristyl alcohol has been reported, mostly in case reports or small test series, in patients with contact dermatitis due to cosmetics or medical ointments. 1-Tetradecanol may be prepared by the hydrogenation of myristic acid (or its esters); myristic acid itself can be found in nutmeg (from where it gains its name) but is also present in palm kernel oil and coconut oil and it is from these that the majority of Myristyl Alcohol is produced. Myristyl Alcohol may also be produced from petrochemical feedstocks via either the Ziegler process or hydroformylation.
Status:
Possibly Marketed Outside US
Source:
Neo-angin
Source URL:
First approved in 1996
Source:
NDA020554
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Dichlorobenzyl alcohol has broad-spectrum activity as an antimicrobial agent and is used in cosmetics and pharmaceuticals. Dichlorobenzyl alcohol has antimicrobial effect against 115 strains of dental plaque. Dichlorobenzyl alcohol inhibited growth of microorganisms but showed highest activity against A. actinomycetemcomitans and Por. gingivalis, organisms related to juvenile and destructive forms of periodontitis. It is a common ingredient in throat lozenges such as Neo angin, Strepsils, Lorsept, and Gorpils. A throat lozenge containing amyl meta cresol and dichlorobenzyl alcohol has a direct virucidal effect on respiratory syncytial virus, influenza A and severe acute respiratory syndrome coronavirus (SARS-CoV).
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:
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:
NDA019822
(1989)
Source URL:
First approved in 1989
Source:
NDA019822
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
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:
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.