Salicylamide Chemical Properties

Melting point:

140-144 °C(lit.)

Boiling point:

270°C

Density 

1,175 g/cm³

refractive index 

1.5323 (estimate)

Flash point:

181°C/14mm

storage temp. 

Inert atmosphere,Room Temperature

solubility 

methanol: 0.1 g/mL, clear

pka

pKa 8.13(H2O t = 37) (Uncertain)

form 

Crystalline Powder

color 

White

Odor

Odorless

PH Range

5 (0.2% aq soln)

Water Solubility 

<0.1 g/100 mL at 20 ºC

Decomposition 

270°C

Merck 

14,8328

BRN 

742439

Stability:

Stable. Light sensitive. Incompatible with strong bases, strong oxidizing agents.

InChIKey

SKZKKFZAGNVIMN-UHFFFAOYSA-N

LogP

1.280

CAS DataBase Reference

65-45-2(CAS DataBase Reference)

NIST Chemistry Reference

Benzamide, 2-hydroxy-(65-45-2)

EPA Substance Registry System

o-Hydroxybenzamide (65-45-2)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22-36/37/38-20/21/22

Safety Statements 

26-36

RIDADR 

3249

WGK Germany 

3

RTECS 

VN6475000

TSCA 

Yes

HazardClass 

6.1(b)

PackingGroup 

III

HS Code 

29214300

Hazardous Substances Data

65-45-2(Hazardous Substances Data)

Toxicity

LD50 orally in mice: 1.4 g/kg (Hart)

MSDS

• Language:English Provider:Salicylamide
• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Salicylamide Usage And Synthesis

Description

Salicylamide is less acidic (pKa 8.2) than other salicylic acid derivatives. Although poorly soluble in water, stable solutions can be formed at pH 9 through ionization of the phenolic group. It is absorbed from the GI tract on oral administration and is rapidly metabolized to inactive metabolites by intestinal mucosa, but not by hydrolysis. Activity appears to reside in the intact molecule. Salicylamide is approximately 40 to 55% plasma protein bound, and it competes with other salicylates and acetaminophen for glucuronide conjugation, decreasing the extent of conjugation of these other drugs.

Chemical Properties

white or light pink crystals or powder

Uses

Medicine (analgesic).

Uses

salicylamide is an analgesic, fungicide, and anti-inflammatory ingredient used to soothe the skin. Salicylamide is an aromatic amide.

Uses

Salicylamide is used in combination with both aspirin and caffeine in the over-the-counter pain remedies. It is used as an analgesic and as an antipyretic.

Definition

ChEBI: The simplest member of the class of salicylamides derived from salicylic acid.

General Description

Salicylamide, o-hydroxybenzamide, is a derivative of salicylicacid that is fairly stable to heat, light, and moisture. Itreportedly exerts a moderately quicker and deeper analgesiceffect than aspirin because of quicker CNS penetration. Its metabolismdiffers from aspirin, because it is not metabolized tosalicylic acid but rather excreted exclusively as the ether glucuronideor sulfate. Thus, as a result of lack of contributionfrom salicylic acid, it has a lower analgesic and antipyretic efficacythan that of aspirin. However, it can be used in place ofsalicylates for patients with a demonstrated sensitivity to salicylates.It is also excreted much more rapidly than other salicylates,which accounts for its lower toxicity. It is available inseveral nonprescription products, in combination with acetaminophenand phenyltoloxamine (e.g., Rid-A Pain compound,Cetazone T, Dolorex, Ed-Flex, Lobac) or with aspirin,acetaminophen, and caffeine (e.g., Saleto, BC Powder).

General Description

Odorless white or slightly pink crystals. Bitter taste, leaves a sensation of warmth on the tongue. pH (saturated aqueous solution at 82°F) about 5. Sublimation begins at the melting point.

Air & Water Reactions

Salicylamide darkens on exposure to air. . Insoluble in water.

Reactivity Profile

Salicylamide is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). Salicylamide may be sensitive to prolonged exposure to light.

Fire Hazard

Flash point data for Salicylamide are not available; however, Salicylamide is probably combustible.

Clinical Use

Whereas salicylamide is reported to be as effective as aspirin as an analgetic/antipyretic and is effective in relieving pain associated with arthritic conditions, it does not appear to possess useful anti-inflammatory activity. Thus, indications for the treatment of arthritic disease states are unwarranted, and its use is restricted to the relief of minor aches and pain at a dosage of 325 to 650 mg three or four times per day. Its effects in humans are not reliable, however, and its use is not widely recommended.

Purification Methods

Crystallise the amide from water or repeatedly from CHCl3 [Nishiya et al. J Am Chem Soc 108 3880 1986]. [Beilstein 10 IV 169.] The anilide [87-17-2] M 213.2, m 135o crystallises from H2O. [Beilstein 12 H 500, 12 I 268, 12 II 256, 12 944.]

Salicylamide(65-45-2)Related Product Information

• Phenoxybenzamine hydrochloride
• Sodium salicylate
• O-ACETYLSALICYLOYL CHLORIDE
• Trimethoprim
• Salicylaldehyde
• 4-Fluorobenzylamine
• Salicylhydrazide
• D-(-)-Salicin
• 2-Ethoxybenzamide
• Salicylanilide
• Sodium 4-aminosalicylate dihydrate
• N-ALPHA-METHYL-L-ALANINE HYDROCHLORIDE
• 3-Methyl-4H-1,2,4-benzothiadiazine 1,1-dioxide
• 6,7-Dichloro-3-methyl-2H-1,2,4-benzothiadiazine 1,1-dioxide
• 4-AMINO-6-CHLORO-BENZENE-1,3-DISULFONYL DICHLORIDE
• HYDROCHLOROTHIAZIDE-3,3-D2
• Hydrochlorothiazide-13C,d2
• 1-CHLOROPHTHALAZINE