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C11006

碳酰肼

Name: 碳酰肼
Brand: ALDRICH

98%

别名:

1,3-二氨基脲, N,N′-二氨基脲, 碳酰二肼, 碳酰肼

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关于此项目

线性分子式:

CO(NHNH₂)₂

化学文摘社编号:

497-18-7

分子量:

90.08

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892343

EC Number:

207-837-2

Beilstein/REAXYS Number:

1747069

MDL number:

MFCD00007591

Assay:

98%

Form:

crystals

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属性

Quality Level

200

assay

98%

form

crystals

mp

150-153 °C (lit.)

SMILES string

NNC(=O)NN

InChI

1S/CH6N4O/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)

InChI key

XEVRDFDBXJMZFG-UHFFFAOYSA-N

说明

Application

碳酰肼用于：

作为除氧剂。
通过缩合反应，与各种醛和配体合成多齿席夫碱配体。
通过环缩合反应合成含三氟甲基的（E）-N′--亚芳基-1-H-吡唑-1-碳酰肼，具有抗氧化剂和抗菌特性。

pictograms

GHS07,GHS09

signalword

Warning

hcodes

H302,H315,H317,H411

pcodes

P273 - P280 - P301 + P312 + P330 - P302 + P352

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1

supp_hazards

EUH044

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Critical assessment of rhBMP-2 mediated bone induction: an in vitro and in vivo evaluation.

Marta Kisiel et al.

Journal of controlled release : official journal of the Controlled Release Society, 162(3), 646-653 (2012-08-21)

Understanding the influence of formulation and storage conditions on rhBMP-2 bioactivity is extremely important for its clinical application. Reports in the literature show that different research groups employ different parameters such as formulation conditions, storage, doses for in vivo applications

Design and synthesis of novel thiophenecarbohydrazide, thienopyrazole and thienopyrimidine derivatives as antioxidant and antitumor agents.

Ameen Ali Abu-Hashem et al.

Acta pharmaceutica (Zagreb, Croatia), 60(3), 311-323 (2010-12-08)

2-Amino-5-acetyl-4-methyl-thiophene-3-carboxylic acid ethyl ester (1) and 5-acetyl-2-amino-4-methylthiophene-3-carbohydrazide (2) were synthesized and used as starting materials for the synthesis of new series of 1-(5-amino-4-(3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3a), 1-(5-amino-4-(4-chloro-3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3b), 1-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl)pyrazolidine-3,5-dione (4), (Z)-N'-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl) formohydrazonic acid (5a), (Z)-ethyl-N'-4-methyl-2-amino-5-acetylthiophene-3-carbonylformo hydrazonate (5b), 6-acetyl-3-amino-2,5-dimethylthieno[2,3-d]pyrimidin-4(3H)-one (8), 5-methyl-3-amino-2-mercapto-6-acetylthieno

Synthesis, antitubercular activity, and SAR study of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides.

Alessandro K Jordão et al.

Bioorganic & medicinal chemistry, 19(18), 5605-5611 (2011-08-16)

Tuberculosis treatment remains a challenge that requires new antitubercular agents due to the emergence of multidrug-resistant Mycobacterium strains. This paper describes the synthesis, the antitubercular activity and the theoretical analysis of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides (8a-b, 8e-f, 8i-j and 8n-o) and new analogues

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全球贸易项目编号

货号	GTIN
C11006-25G	04061833460719
C11006-100G	04061832493077