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辣椒红色素

CAS 465-42-9C40H56O3MW 584.9核心供应

辣椒红色素(CAS 465-42-9):分子式 C40H56O3、分子量 584.9;类别 染料及颜料。

规格参数

CAS号465-42-9
分子式C40H56O3
分子量584.9
熔点176 °C
LogP10.6
应用领域化妆品 colorant、orange 食品 color、E 160(c)
类别着色剂

用途与场景

登记用途:化妆品 colorant、orange 食品 color、E 160(c)。

采购档案

这个产品是什么

辣椒红色素 是一种着色或颜料类化合物,登记 CAS 号为 465-42-9,分子式 C40H56O3(分子量 584.9),归属于染料及颜料大类化工原料。

识别信息

登记 CAS 号:465-42-9

其分子式 C40H56O3 由 40 个碳、56 个氢、3 个氧 组成。

别名/同义词:辣椒红色素 · capsanthin · Paprika extract

所属分类:染料及颜料

常见问题

辣椒红色素 的 CAS 号是多少?

辣椒红色素 的 CAS 登记号为 465-42-9。

辣椒红色素 的分子式与分子量是多少?

分子式 C40H56O3,分子量 584.9。

辣椒红色素 还有哪些别名?

别名/同义词:辣椒红色素、capsanthin、Paprika extract。

辣椒红色素 的登记用途是什么?

登记用途:化妆品 colorant、orange 食品 color、E 160(c)。

辣椒红色素 属于哪个分类?

所属分类:着色剂。

包装与单证

包装按订单确认,从实验室小包装到吨袋大货,随订单安排而非在页面上写死。每批随货附 COA 分析证书,可另提供 MSDS;若终端用途带有法规限度(食品接触、药品或化妆品),请在询价时说明执行标准,等级按该标准确定。

PubChem 公开数据

辣椒红色素(CAS 465-42-9)的公开数据库记录,列此仅供独立核对。

危险化学品分类与危害说明

GHS notification summary100% (11 / 11)

This chemical does not meet GHS hazard criteria for 100% (11 of 11) of all reports.

Reported as not meeting GHS hazard criteria by 11 of 11 companies. For more detailed information, please visit ECHA C&L website.

法规与备案状态

Regulatory & Food ContactCIR / INCI: Cosmetic colorant
GHS notification summary100% (11 / 11)

物理形态与操作说明

  • Deep carmine-red needles from petroleum ether
  • In water, 3.41X10-10 mg/L at 25 °C (estimated)
  • Freely soluble in acetone, chloroform; soluble in methanol, ethanol, ether and benzene; slightly soluble in petroleum ether and carbon disulfide.
  • 4.65X10-18 mm Hg at 25 °C (estimated)
  • Henry's law constant = 2.9X10-8 cu m-atm/mol at 25 °C (estimated)
  • When heated to decomposition it emits acrid smoke and irritating fumes.

公开数据库收录的理化数据

熔点176 °C

这个物质在各数据库里的编号

CAS Registry Number465-42-9
PubChem CID5281228
分子式C40H56O3
IUPAC 名称(2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one
UNII(FDA)420NY1J57N

数据库记载的用途

  • Used as an orange food color, E 160(c)
  • The pharmacokinetics of dietary capsanthin were determined in four male volunteers with plasma essentially free of capsanthin at the beginning of the study. They received paprika juice for 1 week, equivalent to three doses of 5.4 umol capsanthin/day, for a total of 16.2 umol/day. The level of capsanthin in plasma reached a plateau (0.10-0.12 umol/L) between day 2 and day 7, and capsanthin was not detectable in plasma by day 16. Capsanthin was distributed in the plasma lipoproteins after 1 week as follows: very low
  • The bioavailability of carotenoids from a paprika oleoresin (zeaxanthin, beta- cryptoxanthin, beta-carotene, capsanthin, capsorubin) was assessed in humans. After overnight fasting, nine volunteers ingested a single dose of a paprika oleoresin containing 6.4 mg zeaxanthin, 4.2 mg beta-cryptoxanthin, 6.2 mg beta-carotene, 35.0 mg capsanthin and 2.0 mg capsorubin. At different time points, the carotenoid pattern in the chylomicron fraction of whole blood was analyzed to evaluate carotenoid absorption. From the major
  • /A/ study in which rats were gavaged with a mixture of capsaicinoids /was reported/. These substances were extensively metabolized by a variety of metabolic pathways, including 1) hydrolysis of the acid-amide bond and deamination to form vanillylamine, 2) hydroxylation of the vanillyl ring, 3) oxidation of the hydroxyl group in the ring and 4) oxidation of the terminal carbon in the sidechain. /Capsaicinoids/
  • Later steps of carotenoid biosynthesis catalyzed by cyclase enzymes involve the formation of alpha, beta, and kappa-rings. Examination of the primary structure of lycopene beta-cyclase revealed 55% identity with that of antheraxanthin kappa-cyclase. Recombinant lycopene beta-cyclase afforded only beta-carotene, while recombinant antheraxanthin kappa-cyclase catalyzed the formation of beta-carotene from lycopene as well as the conversion of antheraxanthin into the kappa-carotenoid capsanthin. Since the formation of
  • ... In a /study/ involving the single ingestion of paprika juice (equivalent to 34.2 umol capsanthin) The half-lives /after a single ingestion of paprika juice (equivalent to 34.2 umol capsanthin)/ were calculated to be 20.1 +/- 1.3 hr for capsanthin and 222 +/- 15 hr for lycopene. ...

它在各数据库里的别名

Capsanthin; 465-42-9; all-trans-capsanthin; Capsanthin/capsorubin; (3R,3'S,5'R)-3,3'-Dihydroxy-beta,kappa-caroten-6'-one; DTXSID10905012; 420NY1J57N; beta,kappa-Caroten-6'one, 3,3'dihydroxy-; CHEBI:3375; RefChem:31613; DTXCID401334125; 207-364-1; MFCD31726206; 3,3'-Dihydroxy-beta,kappa-caroten-6'one; all trans Capsanthin; EINECS 207-364-1

计算机算出的分子描述符

分子量584.9
XLogP310.6
氢键供体数2
氢键受体数3
可旋转键数11
精确质量584.42294564
单同位素质量584.42294564
拓扑极性表面积57.5
重原子数43
形式电荷0

数据库摘要

Paprika extract · CAS 465-42-9 · C40H56O3. UNII 420NY1J57N. 熔点: 176 °C.

数据来源:PubChem / Wikidata;与随货 COA 不一致时以 COA 为准。

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