5-Aminosalicylic acid , ≥99% , 89-57-6
Synonym(s):
5-Amino-2-hydroxybenzoic acid;5-Aminosalicylic acid;5-AS;Mesalamine
CAS NO.:89-57-6
Empirical Formula: C7H7NO3
Molecular Weight: 153.14
MDL number: MFCD00007877
EINECS: 201-919-1
Pack Size | Price | Stock | Quantity |
5g | RMB24.00 | In Stock |
|
25G | RMB33.60 | In Stock |
|
100G | RMB100.00 | In Stock |
|
500G | RMB401.60 | In Stock |
|
others | Enquire |
PRODUCT Properties
Melting point: | 275-280 °C (dec.) (lit.) |
Boiling point: | 276.03°C (rough estimate) |
Density | 1.3585 (rough estimate) |
vapor pressure | 0Pa at 25℃ |
refractive index | 1.5500 (estimate) |
Flash point: | 279-281°C |
storage temp. | 2-8°C |
solubility | Soluble in dimethyl sulfoxide. |
pka | 2.74, 5.84(at 25℃) |
form | tablets |
color | off-white to gray |
PH | 4.0-4.1 (0.8g/l, H2O, 20℃) |
PH Range | Non-B uorescence (3.1) to light green B uorescence (4.4) |
Water Solubility | <0.1 g/100 mL at 21 ºC |
Decomposition | 279-281 ºC |
Merck | 14,5904 |
BRN | 2090421 |
BCS Class | 4 |
Stability: | Stable. Incompatible with acids, acid anhydrides, acid chlorides, chloroformates, strong oxidizing agents. |
Major Application | Detergent, hair dyes, prevention of colorectal cancer, treating inflammatory bowel disease, autoimmune disorders, gastrointestinal inflammation, chemokine-mediated diseases, mucosal tissue disorder, sleep disorders, rectoanal tenesmus, ulcerative colitis |
InChIKey | KBOPZPXVLCULAV-UHFFFAOYSA-N |
LogP | 0.98 at 25℃ |
CAS DataBase Reference | 89-57-6(CAS DataBase Reference) |
NIST Chemistry Reference | Mesalamine(89-57-6) |
EPA Substance Registry System | Benzoic acid, 5-amino-2-hydroxy- (89-57-6) |
Description and Uses
5-Aminosalicylic acid (5-ASA), also known as mesalazine or mesalamine, is a metabolite and potential pharmacologically active component of sulphasalazine, a drug used in the treatment of Crohn’s disease and ulcerative colitis. However, the mechanism by which this drug works has not been established. In whole blood assays, 5-ASA proves to be a weak, non-selective inhibitor of both COX-1 and COX-2 with IC50 values of 410 and 61 μM, respectively. In ionophore-stimulated colonic mucosal cells, 1 mM 5-ASA does not inhibit prostaglandin E2 (PGE2) production, but does reduce leukotriene B4 (LTB4) synthesis approx. 50%. In ionophore-stimulated human leukocytes, 400 μM 5-ASA reduces LTB4 production approximately 20%. 5-ASA does not inhibit 15-hydroxy PGDH at concentrations up to 50 μM.
5-Aminosalicylic acid is used in the preparation of gastrointestinal anti-inflammatory agents. It is a metabolite of sulfasalazine. It acts as a drug involved in the treatment of Crohn's disease and ulcerative colitis. Further, it is used to make dyes and light-sensitive papers.
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H315-H319-H335 |
Precautionary statements | P305+P351+P338-P261-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a |
Hazard Codes | Xi |
Risk Statements | 36/37/38-52/53 |
Safety Statements | 26-36-24/25-61-37/39 |
WGK Germany | 2 |
RTECS | VO1400000 |
F | 8-10-23 |
Autoignition Temperature | 280 °C |
TSCA | Yes |
HazardClass | IRRITANT |
HS Code | 29225000 |
Hazardous Substances Data | 89-57-6(Hazardous Substances Data) |
Toxicity | LD50 orally in Rabbit: 2800 mg/kg LD50 dermal Rat > 5000 mg/kg |