Pindone
May 1994
Immediately Dangerous to Life or Health Concentrations (IDLH)
CAS number: 83–26–1
NIOSH REL: 0.1 mg/m3 TWA
Current OSHA PEL: 0.1 mg/m3 TWA
1989 OSHA PEL: Same as current PEL
1993-1994 ACGIH TLV: 0.1 mg/m3 TWA
Description of substance: Bright-yellow powder with almost no odor.
LEL:. . Unknown
Original (SCP) IDLH: 200 mg/m3
Basis for original (SCP) IDLH: According to ACGIH [1971], the critical rodenticidal dosages of Pival® (pindone) and warfarin are similar. Therefore, the chosen IDLH is based on an analogy with warfarin which has an IDLH of 200 mg/m3.
Short-term exposure guidelines: None developed
ACUTE TOXICITY DATA:
Lethal dose data:
Species | Reference | Route | LD50 (mg/kg) | LDLo (mg/kg) | Adjusted LD | Derived value |
---|---|---|---|---|---|---|
RatDog
Rabbit |
Gaines 1960Klimmer 1971
Perkow 1971/1976 |
oraloral
oral |
28075
150 |
———-
—– |
1,960 mg/m3525 mg/m3
1,050 mg/m3 |
196 mg/m353 mg/m3
105 mg/m3 |
Other animal data: It has been reported that the critical rodenticidal dosages of Pival® (pindone) and warfarin are similar [ACGIH 1971].
Human data: It has been reported that 50 to 500 mg/kg is the probable lethal oral dose [Gosselin et al. 1984]. [Note: An oral dose of 50 to 500 mg/kg is equivalent to a 70-kg worker being exposed to about 2,330 to 23,300 mg/m3 for 30 minutes, assuming a breathing rate of 50 liters per minute and 100% absorption.]
Revised IDLH: 100 mg/m3Basis for revised IDLH: No inhalation toxicity data are available on which to base an IDLH for pindone. Therefore, the revised IDLH for pindone is 100 mg/m3 based on acute oral toxicity data in humans [Gosselin et al. 1984] and animals [Gaines 1960; Klimmer 1971; Perkow 1971/1976] and an analogy to warfarin [ACGIH 1971] which has a revised IDLH of 100 mg/m3. |
REFERENCES:
1. ACGIH [1971]. Pival (2-pivalyl-1,3-inandione). In: Documentation of the threshold limit values for substances in workroom air. 3rd ed. Cincinnati, OH: American Conference of Governmental Industrial Hygienists, p. 213.
2. Gaines TB [1960]. The acute toxicity of pesticides to rats. Toxicol Appl Pharmacol 2:88-99.
3. Gosselin RG, Smith RP, Hodge HC [1984]. Clinical toxicology of commercial products. 5th ed. Baltimore, MD: Williams & Wilkins Company, p. II-348.
4. Klimmer OR [1971]. Pflanzenschutz und schaedlingsbekaempfungsmittel: abriss einer toxikologie und therapy von vergiftungen. 2nd ed. Hattingen, Germany: Hundt-Verlag, p. 118 (in German).
5. Perkow W [1971/1976]. Wirksubstanzen der pflanzenschutz und schadlingsbekampfungsmittel. Berlin, Germany: Verlag Paul Parey, 1971-1976 (in German).