2,6-Bis(hydroxymethyl)-p-cresol
Names
[ CAS No. ]:
91-04-3
[ Name ]:
2,6-Bis(hydroxymethyl)-p-cresol
[Synonym ]:
2,6-di(hydroxymethyl)-4-methylphenol
EINECS 202-036-4
MFCD00004619
2,6-Bis(hydroxymethyl)-4-methylphenol
2,6-Bis(hydroxymethyl)-p-cresol
1,3-Benzenedimethanol, 2-hydroxy-5-methyl-
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
333.3±11.0 °C at 760 mmHg
[ Melting Point ]:
128-130 °C(lit.)
[ Molecular Formula ]:
C9H12O3
[ Molecular Weight ]:
168.190
[ Flash Point ]:
166.1±13.9 °C
[ Exact Mass ]:
168.078644
[ PSA ]:
60.69000
[ LogP ]:
-0.43
[ Vapour density ]:
5.8 (vs air)
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.613
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- CZ6440000
- CHEMICAL NAME :
- 1,3-Benzenedimethanol, 2-hydroxy-5-methyl-
- CAS REGISTRY NUMBER :
- 91-04-3
- BEILSTEIN REFERENCE NO. :
- 1240237
- LAST UPDATED :
- 199701
- DATA ITEMS CITED :
- 2
- MOLECULAR FORMULA :
- C9-H12-O3
- MOLECULAR WEIGHT :
- 168.21
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LDLo - Lowest published lethal dose
- ROUTE OF EXPOSURE :
- Parenteral
- SPECIES OBSERVED :
- Amphibian - frog
- DOSE/DURATION :
- 1250 mg/kg
- TOXIC EFFECTS :
- Sense Organs and Special Senses (Eye) - miosis (pupillary constriction) Behavioral - altered sleep time (including change in righting reflex) Lungs, Thorax, or Respiration - respiratory depression
- REFERENCE :
- JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 26,123,1926
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
CZ6440000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
J. Am. Chem. Soc. 132(45) , 15842-5, (2010)
An unprecedented single crystal-to-single crystal transformation occurs when a binuclear oxovanadium(V) compound [V(V)(2)O(2)(L)(2)] 1 involving 2,6-bis(hydroxymethyl)-p-cresol (H(3)L) as a bridging l...