Thiosalicylic acid CAS#147-93-3

CAS Number: 147-93-3
Chemical Formula: C7H6O2S
Synonyms:

O-MERCAPTOBENZOIC ACID
O-SULFHYDRYLBENZOIC ACID
Thisosalicyilic acid

Appearance: White Powder

MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)

Қазір хабарласыңыз Электрондық пошта Телефон WhatsApp

Өнім мәліметтері

Thiosalicylic acid CAS#147-93-3

Thiosalicylic acid, (o-mercapto benzoic acid), a sulfur-yellow solid that softens at 158 °C (316 °F), has a melting point of 164 °C (327 °F). It sublimes, is slightly soluble in hot water but freely soluble in glacial acetic acid and alcohol, and yields dithiosalicylic acid, upon exposure to air.

Thiosalicylic acid Chemical Properties

Melting point	162-165 °C (lit.)
Boiling point	247.55°C (rough estimate)
density	1.49
refractive index	1.5100 (estimate)
Fp	150 °C
storage temp.	Store below +30°C.
solubility	DMSO (Slightly), Methanol (Slightly)
form	Fine Crystalline Powder
pka	pK1:4.05(0) (20°C)
color	White to yellow
Water Solubility	soluble in hot water
Sensitive	Air & Light Sensitive
Merck	14,9360
BRN	508507
Cosmetics Ingredients Functions	REDUCING ANTIOXIDANT KERATOLYTIC
InChI	1S/C7H6O2S/c8-7(9)5-3-1-2-4-6(5)10/h1-4,10H,(H,8,9)
InChIKey	NBOMNTLFRHMDEZ-UHFFFAOYSA-N
SMILES	OC(=O)c1ccccc1S
LogP	2.390
CAS DataBase Reference	147-93-3(CAS DataBase Reference)
NIST Chemistry Reference	Benzoic acid, 2-mercapto-(147-93-3)
EPA Substance Registry System	Benzoic acid, 2-mercapto- (147-93-3)

Safety Information

Hazard Codes	Xi,Xn,N
Risk Statements	36/37/38-20/21/22
Safety Statements	26-36/37/39-36
WGK Germany	3
RTECS	DH3325000
F	9-23
TSCA	TSCA listed
HS Code	29309070
Storage Class	11 - Combustible Solids
Hazard Classifications	Eye Irrit. 2 Skin Irrit. 2 STOT SE 3
Hazardous Substances Data	147-93-3(Hazardous Substances Data)
Toxicity	mouse,LD50,intraperitoneal,50mg/kg (50mg/kg),National Technical Information Service. Vol. AD277-689,

Product Application Of Thiosalicylic acid CAS#147-93-3

thiosalicylic acid can be used as:
A nucleophilic trapping agent for the desulfenylation of 3-indolyl sulfides to obtain 3-unsubstituted indoles.
A starting material to prepare 2′-mercaptoacetophenone, which is used in the synthesis of thioflavanone by reacting with lithium diisopropylamide and benzaldehyde.
A stabilizing agent in the synthesis of metal nanoparticles.
It can also be used to prepare 2-thioxanthone-thioacetic acid bimolecular system, which is used as a photoinitiator for free radical polymerization.

Fact Factory and Equipment Show

Gardenia Yellow#94238-00-3