naproxen
(+)-6-methoxy-alpha-methyl-2-naphthalene acetic acid
 
Notes:
Naproxen (INN) is a non-steroidal anti-inflammatory drug (NSAID) commonly used for the reduction of mild to moderate pain, fever, inflammation and stiffness caused by conditions such as osteoarthritis, rheumatoid arthritis, psoriatic arthritis, gout, ankylosing spondylitis, injury (like fractures), menstrual cramps, tendonitis, bursitis, and the treatment of primary dysmenorrhea. Naproxen and naproxen sodium are marketed under various trade names including: Aleve, Anaprox, Naprogesic, Naprosyn, Naprelan; Naproxen is a non-steroidal anti-inflammatory drug (NSAID) commonly used for the reduction of mild to moderate pain, fever, inflammation and stiffness caused by conditions such as osteoarthritis, rheumatoid arthritis, psoriatic arthritis, gout, ankylosing spondylitis, injury (like fractures), menstrual cramps, tendonitis, bursitis, and the treatment of primary dysmenorrhea. Naproxen and naproxen sodium are marketed under various trade names including: Aleve, Anaprox, Naprogesic, Naprosyn, Naprelan. Naproxen was first marketed as the prescription drug Naprosyn in 1976 and naproxen sodium was first marketed under the trade name Anaprox in 1980. It remains a prescription-only drug in much of the world. The U.S. Food and Drug Administration (FDA) approved the use of naproxen sodium as an over-the-counter (OTC) drug in 1991, where OTC preparations are sold under the trade name Aleve. In Australia, small packets of lower-strength preparations of naproxen sodium are Schedule 2 Pharmacy Medicines; Naproxen is a member of the 2-arylpropionic acid (profen) family of NSAIDs. It is an odorless, white to off-white crystalline substance. It is lipid-soluble, practically insoluble in water with a low pH (below pH 4), while freely soluble in water at 6 pH and above. Naproxen has a melting point of 153 degree centigrade. [HMDB]
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      22204-53-1 (S)-Naproxen >98%
      (S)-Naproxen is a non-selective COX inhibitor.
       
       
  • Glentham Life Sciences
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CAS Number: 22204-53-1Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 244-838-7
FDA UNII: 57Y76R9ATQ
XlogP3-AA: 3.30 (est)
Molecular Weight: 230.26318000
Formula: C14 H14 O3
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Food Chemicals Codex Listed: No
Soluble in:
 water, 15.9 mg/L @ 25 °C (exp)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: skin conditioning
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Suppliers:
BOC Sciences
For experimental / research use only.
(S)-Naproxen >98%
Odor: characteristic
Use: (S)-Naproxen is a non-selective COX inhibitor.
Glentham Life Sciences
Naproxen, 98%
Glentham Life Sciences
Naproxen, BP grade
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-child TDLo  2250 mg/kg/26W
SKIN AND APPENDAGES (SKIN): "DERMATITIS, OTHER: AFTER SYSTEMIC EXPOSURE"
British Journal of Rheumatology. Vol. 26, Pg. 210, 1987.

oral-dog LD50  > 1000 mg/kg
Yakkyoku. Pharmacy. Vol. 29, Pg. 861, 1978.

unreported-dog LD50  1000 mg/kg
Journal of Clinical Pharmacology. Vol. 15, Pg. 311, 1975.

oral-guinea pig LD50  665 mg/kg
Archives of Toxicology, Supplement. Vol. 7, Pg. 365, 1984.

oral-hamster LD50  1400 mg/kg
Archives of Toxicology, Supplement. Vol. 7, Pg. 365, 1984.

unreported-hamster LD50  4110 mg/kg
Journal of Clinical Pharmacology. Vol. 15, Pg. 311, 1975.

oral-man TDLo  54 mg/kg
KIDNEY, URETER, AND BLADDER: PROTEINURIS GASTROINTESTINAL: NAUSEA OR VOMITING KIDNEY, URETER, AND BLADDER: HEMATURIA
Journal of Toxicology, Clinical Toxicology. Vol. 33, Pg. 173, 1995.

oral-man TDLo  114 mg/kg/10D-
BLOOD: CHANGES IN PLATELET COUNT
Journal of Clinical Pharmacology. Vol. 40, Pg. 124, 2000.

oral-man TDLo  214 mg/kg/30D-
KIDNEY, URETER, AND BLADDER: OTHER CHANGES IN URINE COMPOSITION LIVER: OTHER CHANGES LIVER: "JAUNDICE, OTHER OR UNCLASSIFIED"
Postgraduate Medical Journal. Vol. 56, Pg. 368, 1980.

oral-man TDLo  3429 mg/kg/35W
VASCULAR: BP ELEVATION NOT CHARACTERIZED IN AUTONOMIC SECTION LUNGS, THORAX, OR RESPIRATION: CYANOSIS
Postgraduate Medical Journal. Vol. 68, Pg. 766, 1992.

intraperitoneal-mouse LD50  500 mg/kg
Bollettino Chimico Farmaceutico. Vol. 119, Pg. 600, 1980.

intravenous-mouse LD50  435 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: EXCITEMENT
Journal of Pharmacology and Experimental Therapeutics. Vol. 179, Pg. 114, 1971.

oral-mouse LD50  360 mg/kg
Farmaco, Edizione Scientifica. Vol. 40, Pg. 334, 1985.

unreported-mouse LD50  1234 mg/kg
Journal of Clinical Pharmacology. Vol. 15, Pg. 311, 1975.

intraperitoneal-rat LD50  354 mg/kg
Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 9, Pg. 829, 1978.

oral-rat LD50  248 mg/kg
Arzneimittel-Forschung. Drug Research. Vol. 41, Pg. 1265, 1991.

Dermal Toxicity:
subcutaneous-mouse LD50 475 mg/kg
Oyo Yakuri. Pharmacometrics. Vol. 6, Pg. 1039, 1972.

subcutaneous-rat LD50 928 mg/kg
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Kiso to Rinsho. Clinical Report. Vol. 17, Pg. 1272, 1983.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: cosmetic agents
Recommendation for naproxen usage levels up to:
 not for fragrance use.
 
Recommendation for naproxen flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
ClinicalTrials.gov: search
Daily Med: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 156391
National Institute of Allergy and Infectious Diseases: Data
 (2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid
Chemidplus: 0022204531
RTECS: UF5275000 for cas# 22204-53-1
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References:
 (2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 156391
Pubchem (sid): 134995706
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C01517
HMDB (The Human Metabolome Database): HMDB01923
FooDB: FDB022741
Export Tariff Code: 2918.90.4000
MedlinePlusSupp: View
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 acusprain
 anexopen
 clinosyn
 danaprox
 flexipen
 genoxen
 laraflex
(+)-(S)-6-methoxy-a-methyl-2-naphthaleneacetic acid
(+)-6-methoxy-alpha-methyl-2-naphthalene acetic acid
(2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid
 nalyxan
 pronaxen
 rheumaflex
 soproxen
 traumox
 veradol
 xenar
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