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辣椒提取物

CAS 465-42-9C40H56O3MW 584.9

济南圣和化工主营供应 辣椒提取物(CAS 465-42-9),归类于食品添加剂,分子式 C40H56O3,分子量 584.9。我们面向国内化工贸易与生产企业提供稳定的现货供应,报价响应快,支持对公转账并可开具增值税发票。

产品概览

CAS号465-42-9
分子式C40H56O3
分子量584.9
熔点176 °C
LogP10.6
纯度按批次COA提供(不公开发布)
包装按订单/批次确认(不公开发布)
应用领域食品添加剂
类别食品添加剂

应用领域

食品添加剂

辣椒提取物在食品添加剂领域使用广泛。采购前请确认纯度等级与包装形式,以批次 COA 为验收依据。

包装与储存

包装规格按订单/批次确认(不公开发布)
纯度规格按批次COA提供(不公开发布)
储存条件密封、阴凉干燥处保存
运输常规化工运输
样品可协商提供
交期现货/按订单安排

供应说明:辣椒提取物 常规包装为按订单/批次确认(不公开发布),储存时应密封置于阴凉干燥处,避免与氧化剂混放。济南圣和化工有限公司 支持国内物流发货,大货交期与运费以订单确认为准。

质量与文件

每批产品随货提供 COA(分析证书);可按需提供 MSDS/技术数据表及第三方检测报告。纯度与包装以批次 COA 及订单确认为准。

关于供应商

作为化工原料供应服务商,济南圣和化工有限公司 长期服务于化工贸易、食品添加、医药中间体、日化原料等行业的采购需求。除 辣椒提取物 外,您还可以在站内按 CAS 号或产品分类检索更多品类,获取规格与报价。

常见问题

辣椒提取物 的 CAS 号是多少?

辣椒提取物 的 CAS 号为 465-42-9。

该产品的纯度和包装规格是什么?

常规纯度规格为 按批次COA提供(不公开发布),包装为 按订单/批次确认(不公开发布),随货提供 COA。

辣椒提取物 有什么用途?

主要应用于食品添加剂。

如何购买或获取报价?

请发送邮件至 info@591daili.com 或通过 WhatsApp 联系,注明产品名称、CAS 号与需求数量,一个工作日内回复报价。供应商:济南圣和化工有限公司。

PubChem 公开数据

Description

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

Identification

CAS Registry Number465-42-9
PubChem CID5281228
Molecular formulaC40H56O3
IUPAC name(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

Computed Descriptors

Molecular Weight584.9
XLogP310.6
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count11
Exact Mass584.42294564
Monoisotopic Mass584.42294564
Topological Polar Surface Area57.5
Heavy Atom Count43
Formal Charge0

Physical & Chemical Properties

Melting Point176 °C

Physical description & handling notes

  • 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.

Regulatory Status

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

GHS Hazard Classification

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.

Documented Uses

  • 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. ...

Synonyms

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

Frequently Asked Questions

What are the CAS number and molecular formula of Paprika extract?

CAS 465-42-9; molecular formula C40H56O3; molecular weight — g/mol.

What other names is Paprika extract known by?

Capsanthin, 465-42-9, all-trans-capsanthin, Capsanthin/capsorubin, (3R,3'S,5'R)-3,3'-Dihydroxy-beta,kappa-caroten-6'-one, DTXSID10905012.

What is the regulatory status of Paprika extract?

Documented regulatory listings: CIR / INCI: Cosmetic colorant.

Is Paprika extract classified as hazardous?

100% of GHS notifications report no hazard classification (11 of 11).

What are the key physical properties of Paprika extract?

Melting Point: 176 °C.

Facts on this page are taken from PubChem (US National Library of Medicine) and Wikidata. Grade-specific data — assay, moisture, particle size, packaging, shelf life — is issued per batch on the COA and is not published here.

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