| Identification | More | [Name]
3,5-Dichlorosalicylic acid | [CAS]
320-72-9 | [Synonyms]
3,5-DICHLORO-2-HYDROXYBENZOIC ACID
3,5-DICHLOROSALICYLIC ACID
RARECHEM AL BE 0032
TIMTEC-BB SBB003480
2-Hydroxy-3,5-dichlorobenzoic acid
2-hydroxy-3,5-dichlorobenzoicacid
3,5-dichloro-2-hydroxy-benzoicaci
3,5-dichloro-salicylicaci
Salicylic acid, 3,5-dichloro-
USAF do-68
usafdo-68
3,5-DICHLOROSSALICYLICACID | [EINECS(EC#)]
206-281-8 | [Molecular Formula]
C7H4Cl2O3 | [MDL Number]
MFCD00002442 | [Molecular Weight]
207.01 | [MOL File]
320-72-9.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R22:Harmful if swallowed. | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3 | [RTECS ]
VO2450000 | [TSCA ]
Yes | [HS Code ]
29182900 | [Safety Profile]
Poison by
intraperitoneal route. When heated to
decomposition it emits toxic fumes of Cl-. | [Hazardous Substances Data]
320-72-9(Hazardous Substances Data) |
| Raw materials And Preparation Products | Back Directory | [Raw materials]
Salicylic acid-->3,5-Dichloro-2-hydroxybenzoic acid methyl ester-->2-(benzyloxy)-3,5-dichlorobenzoic acid-->Sulfosalicylic acid-->5-Chloro-2-hydroxybenzoic acid | [Preparation Products]
2,3,4,6-TETRACHLOROPHENOL-->3,3',4',5-TETRACHLOROSALICYLANILIDE-->2,4,5-Trichlorophenol |
| Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder | [Uses]
3,5-Dichlorosalicylic acid is a bio-active drug and is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase. It also finds its application as medicine and dyes intermediates. | [Definition]
ChEBI: 3,5-Dichlorosalicylicacid is a chlorobenzoic acid. | [General Description]
3,5-Dichlorosalicylic acid is a bio-active drug and its interaction with a model transport protein bovine serum albumin has been investigated. It is a potential inhibitor of human 20α-hydroxysteroid dehydrogenase. |
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