p-Anisidine

CAS number: 104-94-9

NIOSH REL: 0.5 mg/m3 TWA [skin]

Current OSHA PEL: 0.5 mg/m3 TWA [skin]

1989 OSHA PEL: Same as current PEL

1993-1994 ACGIH TLV: 0.1 ppm (0.5 mg/m3) TWA [skin]

Description of substance: Yellow to brown, crystalline solid with an amine-like odor.

LEL: Unknown

Original (SCP) IDLH: 50 mg/m3

Basis for original (SCP) IDLH: Because no data on acute inhalation toxicity are available for anisidine (o-, p-isomers), the chosen IDLH is based on chronic data. ACGIH [1971] reported that mice survived exposures to 10 to 30 mg/m3 for 2 hours/day, 6 days/week for 1 month; a decrease in the excitability of nerves was noted [Zaeva and Fedorova 1962]. Because mice survived 30 mg/m3, 2 hours/day, 6 days/week for 1 month, a worker should be able to escape from 50 mg/m3 without injury or irreversible health effects.

Short-term exposure guidelines: None developed

ACUTE TOXICITY DATA

Lethal dose data:

			LD50	LDLo		Derived
Species	Reference	Route	(Mg/kg)	(mg/kg)	Adjusted LD	Value
Rabbit	IARC 1982	oral	2,900	-----	20,300 mg/m3	2,030 mg/m3
Mouse	IARC 1982	oral	1,300	-----	9,100 mg/m3	910 mg/m3
Mouse	Nippon 1956	oral	-----	1,000	7,000 mg/m3	700 mg/m3
Rat	Sziza and Podragyai 1957	oral	1,400	-----	9,800 mg/m3	980 mg/m3

Other animal data: Mice have survived exposures to concentrations of 10 to 30 mg/m3 for 2 hours/day, 6 days/week for 1 month with a only decrease in the excitability of nerves noted [Zaeva and Fedorova 1962].

Human data: None relevant for use in determining the revised IDLH.

Revised IDLH: 50 mg/m3 [Unchanged] Basis for revised IDLH: Based on subchronic inhalation toxicity data in animals [Zaeva and Fedorova 1962], the original IDLH for p-anisidine of 50 mg/m3 is not being revised at this time.

References:

1. ACGIH [1971]. Anisidine (o-, p-isomers). In: Documentation of the threshold limit values for substances in workroom air. 3rd ed. Cincinnati, OH: American Conference of Governmental Industrial Hygienists, p. 14.
2. IARC [1982]. IARC monographs on the evaluation of carcinogenic risk of chemicals to humans. Vol. 27. Lyon, France: World Health Organization, International Agency for Research on Cancer, p. 63.
3. Nippon Yakurigaku Zasshi (Japanese Journal of Pharmacology) [1956]; 52:215-221 (in Japanese).
4. Sziza M, Podragyai L [1957]. Toxikologische untersuchung einiger in der ungarischen industrie zur anwendung gelangenden aromatischen amidoverbindungen. Arch Gewerbepath Gewerbehyg 15:447-456 (in German).
5. Zaeva GN, Fedorova VI [1962]. Toxsikol Nov Prom Khim Vesh 4:91 (in Russian).