
MSDS等安全信息
- GHS象形图




- GHS符号GHS08 & GHS06 & GHS05 & GHS09;
注释: Health hazard & Skull and crossbones & Corrosion & Environment - 危险类别致癌性 类别2
致突变性 类别2
急性毒性 类别3(吸入)
急性毒性 类别3(经皮)
急性毒性 类别3(经口)
特定目标器官毒性-重复接触 类别1
严重眼损伤 类别1
皮肤致敏 类别1
水生急性毒性 类别1 - 警示词Danger(危险)
- 危险描述H351 |怀疑致癌.
H341 |怀疑导致遗传缺陷.
H331 |吸入会中毒.
H311 |皮肤接触会中毒.
H301 |吞咽会中毒.
H372 |长期或反复接触损害器官.
H318 |造成严重眼损伤.
H317 |可能引起皮肤过敏反应.
H400 |对水生生物毒性极大. - 防范说明P203, P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P308+P316, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
- UN编号1548.0
- 危险品标志T:Toxic;N:Dangerousfortheenvironment;
- 安全声明S26-S27-S36/37/39-S45-S61-S63
- 危险类别码R40:有限证据表明其致癌作用.R41:有严重损伤眼睛的危险.R43:皮肤接触会产生过敏反应.R50:对水生生物极毒.R68:可能有不可挽回的作用的危险R23/24/25:吸入,皮肤接触和不慎吞咽有毒.
- WGK Germany2
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册上下游产品
CAS号98-95-3 硝基苯 | CAS号18740-39-1 2,4-二氯噻吩[2,3-D]嘧啶 | CAS号33228-44-3 4-戊基苯胺 | CAS号461-05-2 DL-肉碱盐酸盐 | CAS号59-88-1 盐酸苯肼 | CAS号3282-99-3 1,1-二(4-氨基苯基)环己烷 | CAS号37529-30-9 4-癸基苯胺 | CAS号538-41-0 对二氨基偶氮苯 | CAS号60-09-3 4-阿基苯甲酯 | CAS号4921-82-8 1-苯酰基-3-苯基硫脲 | CAS号3074-43-9 1-甲基-4-苯基哌嗪 | CAS号100-01-6 对硝基苯胺专利信息
专利号:US-2022389226-A1
优先权日:2019-11-15
标 题:A continuous process for the synthesis of azo dyes involving in-situ generation of diazonium salts
发明人:KULKARNI AMOL ARVIND; SHUKLA CHINMAY ABHAY
权利人:COUNCIL SCIENT IND RES
摘要:The present disclosure provides a continuous process for the synthesis coupled compounds of diazonium salts including azo dyes involving in-situ generation of diazonium salts. It further discloses a set up to carry out the process for the synthesis of coupled compounds of diazonium salts.
专利号:US-4097479-A
优先权日:1977-03-11
标题 :Synthesis of 5-substituted tetrazoles
发明人:LEIPZIG THEODORE J
权利人:MILES LAB
摘要:Synthesis of 5-substituted tetrazoles via reaction of an organic nitrile with azide anion is improved by performing the reaction in an amine as solvent and in the presence of an acid-addition salt of the amine as catalyst.
专利号:US-7576234-B2
优先权日:2002-05-15
标题 :Synthesis of 2-alkyl amino acids
发明人:CHORGHADE MUKUND S; GURJAR MUKUND K; MOHAPATRA DEBENDRA K
权利人:GENZYME CORP
摘要:Non-natural amino acids such as 2-alkylated amino acids allow for the synthesis of a wider variety of peptidal and non-peptidal pharmaceutically active agents. A method of preparing a 2-alkyl amino acid involves a Michael-type addition of a nucleophile to a dialkyl 2-methylidenylpropan-1,3-dioate and the conversion of a ester moiety into an amino moiety. The present invention also discloses a method of preparing a class of iron chelating agents related to desferrithiocin, all of which contain a thiazoline ring. In this method, an aryl nitrile or imidate is condensed with cysteine, a 2-alkyl cysteine, or a cysteine ester.
专利号:US-5861540-A
优先权日:1986-10-29
标题:Substituted 1,1,1-triaryl-2,2,2-trifuoroethanes and processes for their synthesis
发明人:ALSTON WILLIAM B; GRATZ ROY F
权利人:NASA
摘要:Synthetic procedures to tetraalkyls, tetraacids and dianhydrides substituted 1,1,1-triaryl-2,2,2-trifluoroethanes which comprises: (1) 1,1-bis(dialkylaryl)-1-aryl-2,2,2 -trifluoroethane, (2) 1,1-bis(dicarboxyaryl)-1-aryl-2,2,2-trifluoroethane or (3) cyclic dianhydride or diamine of 1,1-bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethanes. The synthesis of (1) is accomplished by the condensation reaction of an aryltrifluoromethyl ketone with a dialkylaryl compound. The synthesis of (2) is accomplished by oxidation of (1). The synthesis dianhydride of (3) is accomplished by the conversion of (2) to its corresponding cyclic dianhydride. The synthesis of the diamine is accomplished by the similar reaction of an aryltrifluoromethyl ketone with aniline or alkyl substituted or disubstituted anilines. Also, other derivatives of the above are formed by nucleophilic displacement reactions.
专利号:US-4758380-A
优先权日:1986-10-29
标题 :Substituted 1,1,1-triaryl-2,2,2-trifluoroethanes and processes for their synthesis
发明人:ALSTON WILLIAM B; GRATZ ROY F
权利人:NASA
摘要:Synthetic procedures to tetraalkyls, tetraacids and dianhydrides substituted 1,1,1-triaryl-2,2,2-trifluoroethanes which comprises: (1) 1,1-bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethane, (2) 1,1-bis(dicarboxyaryl)-1-aryl-2,2,2-trifluoroethane or (3) cyclic dianhydride or diamine of 1,1-bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethanes. The synthesis of (1) is accomplished by the condensation reaction of an aryltrifluoromethyl ketone with a dialkylaryl compound. The synthesis of (2) is accomplished by oxidation of (1). The synthesis dianhydride of (3) is accomplished by the conversion of (2) to its corresponding cyclic dianhydride. The synthesis of the diamine is accomplished by the similar reaction of an aryltrifluoromethyl ketone with aniline or alkyl substituted or disubstituted anilines. Also, other derivatives of the above are formed by nucleophilic displacement reactions.
专利号:US-4912238-A
优先权日:1986-10-29
标 题:Substituted 1,1,1-triaryl-2,2,2-trifluoroethanes and processes for their synthesis
发明人:ALSTON WILLIAM B; GRATZ ROY F
权利人:NASA
摘要:Synthetic procedures to tetraalkyls, tetraacids and dianhydrides substituted 1,1,1-triaryl-2,2,2-trifluoroethanes which comprises: (1) 1,1-bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethane, (2) 1,1-bis(dicarboxyaryl)-1-aryl-2,2,2-trifluoroethane or (3) cyclic dianhydride or diamine of 1,1-bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethanes. The synthesis of (1) is accomplished by the condensation reaction of an aryltrifluoromethyl ketone with a dialkylaryl compound. The synthesis of (2) is accomplished by oxidation of (1). The synthesis dianhydride of (3) is accomplished by the conversion of (2) to its corresponding cyclic dianhydride. The synthesis of the diamine is accomplished by the similar reaction of an aryltrifluoromethyl ketone with aniline or alkyl substituted or disubstituted anilines. Also, other derivatives of the above are formed by nucleophilic displacement reactions.