CAS: 12738-64-6; Saccharose Benzoate

该化合物是硫酸和苯甲酸的酯,其特征是用作食品添加剂和乳化剂,通常用于增强各种食品的质质质和稳定性.这种复合物的特性使其可以作为表面活性剂发挥作用,提高配方成分的溶解性和分散性.苏克罗斯苯甲酸盐的毒性较低,被认为在规定的限度内可以安全消费.它溶于有机溶剂,在水中溶解性有限,因此在需要乳化的特定应用中有用.此外,苏克罗苯甲酸盐可产生甜味,适合用于授精剂和其他甜食产品.它形成稳定的乳液和泡沫的能力在食品和化妆品行业都很宝贵,有助于对使用这些产品的总体感官体验.

英文名称Saccharose Benzoate
中文名称苯甲酸与(2R,3R,4S,5S,6R)-2-(((2S,3S,4S,5R)-3,4-二羟基-2,5-双(羟甲基)四氢呋喃-2-基)的化合物氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇(1:1)
IUPAC名称benzoic acid--(2R,3R,4S,5S,6R)-2-(((2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (1/1)
其它别名β-D-Fructofuranosyl ; Sucrose Octabenzoate
CAS编号12738-64-6
MFCD编号:MFCD00047542
EINECS号:235-795-5
FDA UNII编号:324V957SP6
分子式:C19H28O13
分子量:464.42
产品CID: 435398
产品分类有机原料→分子砌块→手性化合物→手性砌块

相似结构搜索
InChIKey: AKIVKIDZMLQJCH-KWOGCLBWSA-N
JWBMVCAZXJMSOX-LURJTMIESA-N…
计算化学: 氢键受体数12.0氢键供体数9.0可旋转键数6.0

相似化合物

57-50-1 6147-31-5 25702-74-3

物理性质

熔点93-100°C
沸点250°C[at 101 325 Pa]
闪点261.51 °C
密度1.299[at 20°C]
PSA:226.83
LogP:-4.0108
折射率1.657
蒸汽压0Pa at 20°C
溶解性Aromatics, Ketones And Esters: Soluble
外观形态白色至类白色粉末
储存条件Store at room temperature, keep dry and cool
产品应用蔗糖苯甲酸酯(12738-64-6)的用途:本品用作油漆,油墨,塑料助剂.

MSDS等安全信息

GHS象形图
GHS符号GHS08;
注释: Health hazard
危险类别特定目标器官毒性-重复接触类别2
生殖毒性类别1A
水生慢性毒性类别4
警示词Warning(警告)
危险描述H373 |长期或反复接触可能损害器官.
H360 |可能损害生育能力或胎儿.
H413 |可能对水生生物造成长期有害影响.
防范说明P260-P501
WGK Germany3

欧盟法规

REACH注册C&L通报REACH预注册

上下游产品

lithium aluminium tetrahydride O-Methylhydroxylamin lithiumferr°Cene N-benzyloxyamine

合成工艺路线路线简述

海关参考信息

2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇
💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
详情请参考：📖 海关编码查询和海关进出口税则

专利信息

专利号:US-2003072716-A1
优先权日:2001-06-22
标题:Renewable, carbohydrate based CO2-philes
发明人：POOVATHINTHODIYIL RAVEENDRAN; WALLEN SCOTT L
摘要:A composition is disclosed comprising a carbohydrate-based material a dispersed in carbon dioxide. A general method for synthesizing inexpensive, renewable, non-toxic, non-fluorous, carbohydrate based CO 2 -philes is disclosed. These CO 2 -philes are soluble in carbon dioxide. Methods of making the composition are also disclosed. The methods and composition are useful in a variety of applications and can utilize gaseous, liquid and supercritical carbon dioxide. The methods and compositions are useful in the synthesis of surfactants and metal chelates for CO 2 , as a sizing substrate, in CO 2 -based coating processes, for impregnation and plasticizing cellulosic and non-cellulosic materials, in pharmaceutical applications, such as crystallization, dispersion and encapsulation of bioactive molecules in solid systems, in the densification of CO 2 , in the synthesis of biodegradable polymers in CO 2 , and for carbon dioxide removal, to name just a few.