Home Categories API 5-Aminosalicylic acid
A0790512

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
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Update time: 2022-07-08

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℃

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
8-10-23
Autoignition Temperature 280 °C
TSCA  Yes
HazardClass  IRRITANT
HS Code  29225000
Toxicity LD50 orally in Rabbit: 2800 mg/kg LD50 dermal Rat > 5000 mg/kg

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