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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

Articles

Single crystal-to-single crystal irreversible transformation from a discrete vanadium(V)-alcoholate to an aldehydic-vanadium(IV) oligomer.

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...


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