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SDP‐αEDVL
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5. 6 NTP TR 366 1989 200 mg kg day 100 mg kg day NTP TR 366 1989 2 2 2 A 1989 2 SY li 1 1 2 48 LC50 40mg L SIDS 2004 3
6. 2005 05 24 2014 6 30 SDP oeEDVL 130 0026 2 10 14 03 5600 1475 ea L Eco GHS 1 1 1 1 1B 2 2 2
7. SOx
8. 9 1 0 11 gt ACGIH TWA ACGIH STEL C E 10 0 at25 1 10 1 20 8 LD 8 16 2001
9. EHC 157 1994 V79 f ACGIH A3 ACGIH 2008 5 in vitro i IARC 71 1999 n IARC 71 1991 MNO SE IARC 71 1999 ACGIH gt 2 NTP TR 366 1989 NTP TR 366 1989
10. UN1824 8 2 1 5 1 No 336 b ke1 1 6 CHRIP GHS
11. 0 5 124 4 ara 4 15 24 SIDS 2009 ACGIH 7th pH 12 0 05 w w Merck 14th 2006 0 5 SIDS 2009 EHC 157 1994 SIDS Access on Apr 2012 JIS f a NN TD 3 cs EE 3 DFGMAK Doc 4 ST 1 5 10 1998
12. 2 13 1 70 1975 ll E E 2 BOD 25 100 mg kg day 15 2 100 mg kg day NTP TR 366 96 LC50 0 044 mg L NITE 2008 Pseudokirchneriel1a subcapitata 2 0 0015 mg L 10 2010
13. 2 5 6 8
14. EHC 157 1994 LD50 200 mg kg EHC 157 1994 1 1 F344 SD B6C3F1 RW DFGMAK Doc 10 1998 i 15 25 mg kg day
15. Con 157 1994 BHC 157 1994 I E 1 72 9 4r 114 C08 OW 1 9 Access on Apr 0 1 22 1 4 2 5 MM i Mj SIDS 2009 RM ACGIH 7th 2001 corrosive damage et ami A E
16. EU 50 2N 8 4N 16 2mg m3 lmg m3 2mg m3 pH at25C 12 5 13 5 lt 3 LD50 237mg Kg LD50 320mg Kg 6N 24 0 S0x 3 5 4 1 C R35 10 0 25 1 0 HH 55 61 g kg
17. 2 Cas No 1 410 1310 73 2 1 5 3 543 123 31 9 2 2 1 502 7757 83 7 10 15 7732 18 5 gt 50 57 2 18 2 57 2 18 2 2 2 1 No 336 4
18. NN 2 PATTY 5th 2001 1 SIDS 2009 28 0 SIDS 2009 NE O00 BHC 157 1994 DFGMAK Doc 10 1998 LD50 627 743 mg kg
19. 21 NOEC 0 003 mg L 10 2010 0 1 96 LC50 0 044 mg L NITE 2008 2 BOD 70 1975 1og Kow 0 59 PHYSPROP Database 2009 1 1 3 1 4
20. 3 2004 OECD TG 406 70 7 10 strong sensitizer EHC 157 1994 xl strong sensitizer vivo EHC in vivo EHC 157 1994 1B 114 2008 vivo NTP DB 1979
21. 2 1 2 2 pH 12 0 05 w w Merck 14th 2006 1 a NN DFGMAK Doc EU 100 mg 10 1998 48 DFGOTvo1 12 1999 C R35 14 0 f 1 50 5 10 EHC 157 1994 tact Dermatitis 5th 2011
22. PEU Cat 3 R40 EC JRC ESIS Access on Apr 2012 2 OECD TG 416 0 114 2008 OECD TG 414 300 mg kg 114 2008 0 N50 NE Ke 150 mg kg
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