Basic information
- Standard SMILES
O=S(O)CO- InChIKey
SBGKURINHGJRFN-UHFFFAOYSA-N- Molecular formula
- CH4O3S
- Average molar mass
- 96.11 g/mol
- Monoisotopic mass
- 95.98811499
Overview
antidote for mercury poisoning; RN given refers to parent cpd; structure
Names & identifiers
- Preferred name
- Hydroxymethanesulfinic Acid
- IUPAC
- hydroxymethanesulfinic acid
- English name
- Sodium hydroxymethanesulphinate
- Molecular formula
- CH3NaO3S
- Molecular weight
- 119.1
Names & synonyms
Hydroxymethanesulfinic acid79-25-4FormaldehydesulfoxylateDTXSID7048083M049N73196Hydroxymethanesulfinic acid, monosodium saltRefChem:600241DTXCID8028054201-189-4Hydroxymethanesulphinic acidFormaldehyde Sulfinic AcidMFCD00128934
Show more names
RONGALITESODIUM FORMALDEHYDE SULFOXYLATESODIUM HYDROXYMETHANESULFINATERONGALITE CSODIUM FORMALDEHYDESULFOXALATEFORMALDEHYDE SODIUM SULFOXYLATEFORMOSULSodium sulfinomethanolateNatriumhydroxymethansulfinatSodiumbisulfoxylateformaldehyde
UNII-M049N73196EINECS 201-189-4Formaldehydsulfoxylsaurestarbld0012097NCIOpen2_000709SCHEMBL20249Methanesulfinic acid, hydroxy-CHEMBL2111064
Database identifiers
- CAS
149-44-0、79-25-4- PubChem CID
- 9000
- DTXSID
DTXSID7048083- ChEMBL
CHEMBL2111064- UNII
- M049N73196
- EC Number
- 201-189-4
- Nikkaji
- J192.570I
Properties
Computed structural properties
- XLogP
- -1.2
- Topological polar surface area
- 76.7 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 1
- Heavy atoms
- 5
- Formal charge
- 0
- Complexity
- 42.2
Experimental & physicochemical properties
Chemical ClassesOther Classes -> Sulfur Compounds
Collision Cross Section112.7 Ų [M-H]- [CCS Type: DT; Buffer gas: N2; Ionization: ESI-; Dataset: TOXCAST; Source Identifier: DTXSID4049030]
Physicochemical properties
- Melting point
- 120 °C · ~120 °C (dec.)
- Density
- 1.744 · 1.744[at 20℃]
- vapor pressure
- 0.003 Pa · 0.003Pa at 20℃
- Flash point
- 100 ℃ · >100℃
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- 2 O: · H2O: 50 mg/mL, clear, colorless
- form
- Solid
- color
- White to Off-White
- PH
- 9.5 · 9.5-10.5
- Odor
- Mild garlic odor
- Water Solubility
- 2 O, · soluble H2O, alcohol [HAW93]
- Merck
- 14 · 14,8620
- Stability
- Stable. Incompatible with strong oxidizing agents.
- Cosmetics Ingredients Functions
- REDUCING
- LogP
- -3.4 at · -3.4 at 22℃
- Indirect Additives used in Food Contact Substances
- SODIUM FORMALDEHYDESULFOXYLATE
- FDA 21 CFR
- 175.105 · 175.105; 176.170; 177.1210;177.2600
- FDA UNII
- 4 ZGP7K714 · X4ZGP7K714
- EPA Substance Registry System
- Sodium sulfoxylate formaldehyde (anhydrous) (149-44-0)
- Symbol(GHS)
- 7 · GHS07,GHS08
- Signal word
- Warning
- Hazard statements
- 341 · H341-H315-H319-H335
- Precautionary statements
- 280 · P280-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36 · 36/37/38-68-31
- Safety Statements
- 26 · 26-36-36/37
- WGK Germany
- 1 · 1
- RTECS
- 380000 · PB0380000
- TSCA
- TSCA listed
- HS Code
- 2930909899 · 2930909899
- Hazardous Substances Data
- 149 · 149-44-0(Hazardous Substances Data)
- REACH Registrations
- Active
Safety & regulation
Hazard information
Hazards SummarySee Sodium formaldehydesulfoxylate
Safety & protection
Protective Action Criteria (PAC)
6.0 [mg/m3]
66 [mg/m3]
400 [mg/m3]
Safety data
- wgk
- 1
- tsca
- TSCA listed
- rtecs
- PB0380000
- hs_code
- 2930909899
- risk_code
- 36/37/38-68-31
- Signal word
- Warning
- Symbol(GHS)
- GHS07,GHS08
- hazard_code
- Xi,Xn
- safety_code
- 26-36-36/37
- Hazard statements
- H341-H315-H319-H335
- REACH Registrations
- Active
- Precautionary statements
- P280-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
- Hazardous Substances Data
- 149-44-0(Hazardous Substances Data)
Chemistry & industry
Uses & manufacturing
UsesAntidote for mercury poisoning. [ChemIDplus]
Applications
UsesPharmaceutic aid (preservative).
UsesSodium Hydroxymethanesulfinate Hydrate is the hydrated version of Sodium Hydroxymethanesulfinate (S634950), which is an organic reductant that is stable in alkaline enviroments but readily decomposes in acidic medium to produce a number of products, one of them being sulfur dioxide. Sodium hydroxymethanesulfinate is also used in conjunction with substituted anilines (e.g. p-Anisidine [A673505]) to synthesize anilinomethanesulfonates.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
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Related reactions
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