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P45850

哌啶甲酸

Name: 哌啶甲酸
Brand: ALDRICH

98%, for peptide synthesis

别名:

(±)-哌啶-2-羧酸, 2-哌啶甲酸, 哌啶甲酸游离碱, 高脯氨酸

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关于此项目

经验公式（希尔记法）:

C₆H₁₁NO₂

化学文摘社编号:

535-75-1

分子量:

129.16

NACRES:

NA.22

PubChem Substance ID:

24898555

UNSPSC Code:

12352106

EC Number:

208-616-3

MDL number:

MFCD00064347

Beilstein/REAXYS Number:

81095

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属性

产品名称

哌啶甲酸, 98%

Quality Level

100

assay

98%

form

powder and chunks

reaction suitability

reaction type: solution phase peptide synthesis

technique(s)

LC/MS: suitable

color

white to beige

mp

282 °C (dec.) (lit.)

SMILES string

OC(=O)C1CCCCN1

InChI

1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)

InChI key

HXEACLLIILLPRG-UHFFFAOYSA-N

说明

General description

派可林酸又名2-哌啶甲酸，是一种多功能试剂，用于液相多肽合成法。通常用作许多拟肽合成中的脯氨酸替代物。

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pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism.

D M Danks et al.

The Journal of pediatrics, 86(3), 382-387 (1975-03-01)

Studies of eight patients with this syndrome confirm the characteristic pattern of abnormalities and the autosomal recessive mode of inheritance. The incidence is estimated to be approximately 1 in 100,000 live births. The liver lesion proved to be variable, with

Conformational heterogeneity about pipecolic acid peptide bonds: conformational, thermodynamic, and kinetic aspects

WJ Wu, et.al.

The Journal of Organic Chemistry, 63, 6689-6698 (1998)

Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction.

B T Poll-The et al.

Journal of inherited metabolic disease, 9(2), 169-174 (1986-01-01)

Infantile Refsum's disease was diagnosed in three male patients, presenting with facial dysmorphia, retinitis pigmentosa, neurosensory hearing loss, hepatomegaly, osteopenia and delayed growth and psychomotor development. An elevated plasma phytanic acid concentration and a deficient phytanic acid oxidase activity in

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全球贸易项目编号

货号	GTIN
P45850-100G	04061833385753
P45850-25G	04061834374831