物理性质
- 熔点-24 °C
- 沸点208.0±0.0 °C at 760 mmHg
- 闪点78.3±0.0 °C
- 密度1.2±0.1 g/cm3
- PSA:60.98
- LogP:1.14
- 折射率1.426
- 蒸汽压0.3±0.3 mmHg at 25°C
- 溶解性溶于乙醚,乙醇
- 敏感性1.若遇高温可发生剧烈分解,引起容器破裂或爆炸事故。遇叔丁氧基钾剧烈反应。遇潮气易分解,生成腐蚀性液体硫酸。2.稳定性 稳定3.禁配物 强氧化剂、强碱、水4.避免接触的条件 潮湿空气、受热5.聚合危害 不聚合6.分解产物 氧化硫
- 外观形态透明油性液体
- 储存条件储存注意事项储存于阴凉、干燥环境、通风良好的库房。远离火种、热源。保持容器密封保存。应与氧化剂、碱类、食用化学品分开存放,切忌混储。配备相应品种和数量的消防器材。储区应备有泄漏应急处理设备和合适的收容材料。
- 产品应用用于有机合成中作乙基化剂.
- 性质描述无色油状液体.熔点-24.5°C,沸点208°C(稍有分解),96°C(2.0kPa),相对密度1.180(18/0°C),折光率1.4010(18°C),闪点78°C.能与醇,醚混溶,不溶于水,遇水慢慢分解,在热水中剧烈分解为硫酸单乙酯和醇.有薄荷香.
MSDS等安全信息
- GHS象形图



- GHS符号GHS08 & GHS07 & GHS05;
注释: Health hazard & Exclamation mark & Corrosion - 危险类别致癌性 类别1B
Muta. 1B
急性毒性 类别4(吸入)
急性毒性 类别3(经皮)
急性毒性 类别4(经口)
皮肤腐蚀 类别1B
急性毒性 类别4(经皮)
严重眼损伤 类别1
急性毒性 类别3(吸入)
水生慢性毒性 类别3 - 警示词Danger(危险)
- 危险描述H350 |可能致癌.
H340 |可能导致遗传缺陷.
H332 |吸入有害.
H311 |皮肤接触会中毒.
H302 |吞咽有害.
H314 |造成严重皮肤灼伤和眼损伤.
H312 |皮肤接触有害.
H318 |造成严重眼损伤.
H331 |吸入会中毒.
H412 |对水生生物有害并具有长期持续影响. - 防范说明P203, P260, P261, P262, P264, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P318, P321, P330, P361+P364, P363, P403+P233, P405, and P501
- UN编号1594.0
- 危险品标志T:Toxic;
- 安全声明S53-S45
- 危险类别码R20/21/22,R34,R45,R46
- WGK Germany3
欧盟法规
统一分类与标签REACH注册ECHA物质工作场所安全标识要求ECHA物质食品接触材料-禁用CMR物质C&L通报化妆品禁用物质清单REACH预注册欧盟候选物质清单废弃物危险特性清单上下游产品
CAS号3141-12-6 乙氧基砷 | CAS号64-17-5 乙醇 | CAS号122-52-1 亚磷酸三乙酯 | CAS号88-12-0 N-乙烯基吡咯烷酮 | CAS号54509-73-8 ethene | CAS号7446-11-9 三氧化硫 | CAS号625-01-4 氯磺酸乙酯 | CAS号105-58-8 碳酸二乙酯 | CAS号60-29-7 乙醚 | CAS号546-74-7 乙基硫磺酸钠 | CAS号110700-49-7 齐墩果酸乙酯 | CAS号108593-47-1 3-乙氧基苯甲酸甲酯 | CAS号57102-97-3 3-溴-9-乙基咔唑 | CAS号429-06-1 四乙基四氟硼酸铵 | CAS号5520-66-1 对二乙氨基苯乙酮 | CAS号58494-59-0 1-乙基-1H-吲哚-3-甲醛 | CAS号40497-11-8 2,3-二氰基丙酸乙酯 | CAS号583-19-7 邻溴苯乙醚 | CAS号429-07-2 四乙基六氟磷酸铵 | CAS号33255-13-9 3,6-二溴-9-乙基咔唑乙烯置于硫酸,水体系中,30.0~125.0 °C,6.86 Mpa 条件下,反应生成 硫酸二乙酯
参考文献:Process For The Sulphation Of Ethylene And The Sulphation Of Alpha Mixture Of Ethylene And Propylene
标题:Process For The Sulphation Of Ethylene And The Sulphation Of Alpha Mixture Of Ethylene And Propylene
专利信息
专利号:US-2024082435-A1
优先权日:2021-02-26
标 题 :Solid phase synthesis of glutamate-urea-lysine derived (GUL derived) prostate-specific membrane antigen (PSMA) targeting conjugates and their use as precursors for therapeutic and/or diagnostic agents
发明人:PINTO ARTUR; BONTEMPS ALEXIS; LEMAIRE LUCAS
权利人:TELIX INT INNOVATIONS PTY LTD
摘要:The disclosure provides methods for the solid phase synthesis of glutamate-urea-lysine derived (GUL derived) prostate-specific membrane antigen (PSMA) targeting conjugates. The disclosure also relates to key intermediates of this process and methods for their preparation such as a method of preparing a compound of formula (V). Also disclosed are use of the conjugates as precursors for therapeutic and/or diagnostic agents, including treating and diagnosing prostate cancer.
专利号:US-4035425-A
优先权日:1973-04-23
标 题 :Synthesis of Vitamin A, intermediates and conversion thereof to Vitamin A
发明人:OROSHNIK WILLIAM
权利人:SCM CORP
摘要:A synthesis of novel Vitamin A intermediates from beta-ionone is described as well as a conversion of the intermediates to Vitamin A. The length of the conjugated aliphatic side chain of beta-ionone is increased while still ultimately obtaining the desired trans form of Vitamin A. In general, beta-ionone is ethynylated to ethynyl-beta-ionol, the hydroxyl of which is etherified to form an ethynyl-terminated, alkoxy-substituted, beta-ionol intermediate. The intermediate is coupled through its copper derivative with a compound like chloro-isopentenyl acetate to produce a C20 skeleton. By semi-hydrogenation, the acetylenic bond on the C20 skeleton is converted to an ethylenic bond, and by hydrolysis the terminal ester moiety is converted to a hydroxyl group. Treatment with a strong base removes the alkoxy group to produce Vitamin A.
专利号:US-4092366-A
优先权日:1975-04-10
标题:Synthesis of Vitamin A, intermediates and conversion thereof to Vitamin A
发明人:OROSHNIK WILLIAM
权利人:SCM CORP
摘要:A synthesis of novel Vitamin A intermediates from betaionone is described as well as a conversion of the intermediates to Vitamin A. The length of the conjugated aliphatic side chain of beta-ionone is increased while still ultimately obtaining the desired trans form of Vitamin A. In general, beta-ionone is ethynylated to ethynyl-beta-ionol, the hydroxyl of which is etherified to form an ethynyl-terminated, alkoxy-substituted, beta-ionol intermediate. The intermediate is coupled through its copper derivative with a compound like chloro-isopentenyl acetate to produce a C20 skeleton. By semi-hydrogenation, the acetylenic bond on the C20 skeleton is converted to an ethylenic bond, and by hydrolysis the terminal ester moiety is converted to a hydroxyl group. Treatment with a strong base removes the alkoxy group to produce Vitamin A.
专利号:US-6417380-B1
优先权日:1987-12-31
标 题 :Synthesis of 1,2-dioxetanes and intermediates therefor
发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
摘要:Compounds having the formula: n wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., n m-phenylene), produced by reacting a compound having the formula: n with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: n are produced by reacting a compound having the formula: n with n wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula n are produced by reacting a compound of the formula n with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.
专利号:US-3983145-A
优先权日:1973-11-01
标 题:Use of alpha-di(lower alkoxy) anthraquinones in the synthesis of Alizarin Saphirols
发明人:WHITE DAVID L; FITZPATRICK JOSEPH W
权利人:TOMS RIVER CHEMICAL CORP
摘要:Alpha-dihydroxyanthraquinones used as intermediates in the synthesis of many dyestuffs, such as the Alizarin Saphirols (e.g. Color Constitution No. 63000, 63005, 63010, 63011, 63315 and 63610) can be replaced on an equimolar basis by alpha-di(lower alkoxy)anthraquinones. The alpha-di(lower alkoxy) anthraquinones can be converted in a single step, by treatment with oleum, to the corresponding alpha-dihydroxyanthraquinone-beta-disulfonic acids in almost quantitative yield. The corresponding diamine is obtained by dinitrating followed by reduction of the nitro groups. The known intermediate, leuco 1,4,5,8-tetrahydroxyanthraquinone (see C.I. No. 62500) can be obtained either by reduction of the diamine or by reduction of the dinitro compound. In one embodiment, the alpha-di(lower alkoxy)anthraquinone is obtained from dinitroanthraquinone by treatment thereof with methanol and KOH.
专利号:US-4756739-A
优先权日:1985-12-21
标题 :Pyridine derivatives and the N-oxides thereof, and the use thereof as intermediates for the synthesis of plant protecting agents
发明人:FUSS ANDREAS; KOCH VOLKER
权利人:HOECHST AG
摘要:The compounds of the formula I (I) in which A denotes N or N->O, Z denotes O or NH, R denotes H, (halo)alkyl, (halo)alkenyl, (halo)alkynyl or alkoxycarbonyl, R1 denotes hydrogen, halogen, amino, -NHOH, hydroxyl, (substituted) phenylazo or a radical of the formulae Y=C=N-, Y1Y2C=N-, Y3NH- or K denotes 0 or 1, and m and n, independently of one another, denote a number from 1 to 4, with the proviso that, when Z-R denotes OH or NH2, (R1)n denotes at least one radical of the formula or represents two radicals, in the 5 or 6 position of the heterocyclic ring, which, in the 5 position, denote halogen and, in the 6 position, denote a radical of the group comprising halogen, amino, hydroxyl or phenylazo, which may be substituted as specified above, are valuable intermediates in the synthesis of plant protection agents.