推荐产品
等级
FG
Kosher
质量水平
管理合规性
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 184.1835
蒸汽密度
<1 (vs air)
蒸汽压
<0.1 mmHg ( 25 °C)
描述
derived from GMO corn
表单
crystals or granules
powder or chunks
旋光性
[α]20/D +104°, c = 0.4 in acidified ammonium molybdate
mp
98-100 °C (lit.)
应用
flavors and fragrances
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一般描述
D-山梨醇是一种糖醇，常用作食品工业中的人造甜味剂、抗结块剂、乳化剂、保湿剂、增稠剂和调味剂。
应用
- 食蚜瘿蚊滞育的分子相关性。: 本研究探讨了捕食性动物食蚜瘿蚊滞育的分子机制，强调了在这种状态下ᴅ-山梨醇在代谢调节中的作用。（Sharma et al., 2024）。
- 代糖对儿童和青少年恒牙龋齿的预防：系统评价和荟萃分析。: 该系统综述评估了各种代糖（包括D-山梨醇）在预防儿童和青少年龋齿方面的有效性。（Luo et al., 2024）。
- 增进玉米麸皮阿拉伯糖基木聚糖薄膜的机械性能以实现可持续食品包装。: 研究了使用D-山梨醇来改善可生物降解薄膜的机械性能，目的在于创造出可持续的食品包装解决方案。（Alahmed & Simsek, 2024）。
- 骆驼明胶薄膜的开发和表征：骆驼骨龄和甘油或山梨醇对薄膜性质的影响。.: 该研究考察了D-山梨醇对骆驼明胶薄膜性质的影响，研究的目的在于提高生物聚合物材料的质量。（Al-Hassan, 2024）。
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Encyclopedia of Food and Color Additives, 2, 2627-2627 (1997)
Daily intake assessment of saccharin, stevioside, D-sorbitol and aspartame from various processed foods in Korea.
Chung MS, et al
Food Additives and Contaminants, 22(11), 1087-1097 (2005)
Reddy Ranjith K Sama et al.
Journal of cellular physiology, 228(11), 2222-2231 (2013-04-30)
FUsed in Sarcoma/Translocated in LipoSarcoma (FUS/TLS or FUS) has been linked to several biological processes involving DNA and RNA processing, and has been associated with multiple diseases, including myxoid liposarcoma and amyotrophic lateral sclerosis (ALS). ALS-associated mutations cause FUS to
G Molino et al.
The Journal of laboratory and clinical medicine, 131(5), 393-405 (1998-05-30)
D-Sorbitol (SOR) is safe, is easy to measure, and has an exceptionally high extraction ratio in the normal liver of 0.93+/-0.05 (mean+/-SD). Together with the general interest in hepatic hemodynamics, these facts motivated us to review the usefulness of this
Shahram Attarian et al.
Orphanet journal of rare diseases, 9, 199-199 (2014-12-19)
Charcot-Marie-Tooth type 1A disease (CMT1A) is a rare orphan inherited neuropathy caused by an autosomal dominant duplication of a gene encoding for the structural myelin protein PMP22, which induces abnormal Schwann cell differentiation and dysmyelination, eventually leading to axonal suffering
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