物质信息
ID:341948
名称和标识
别名
Hydroxylammonium chloride盐酸羟胺Hydroxylamine hydrochloride羟胺 盐酸盐
IUPAC传统名
hydroxylamine hydrochloride
IUPAC标准名
hydroxylamine hydrochloride
化合物性质
安全信息
GHS危险品标识
呼吸道过敏，类别1
生殖细胞突变，类别1A，1B，2
致癌性，类别1A，1B，2
生殖毒性，类别1A，1B，2
特定目标器官毒性 – 一次接触，类别1,2
特定目标器官毒性 – 反复接触，类别1,2
吸入危险，类别1
腐蚀金属，类别1
腐蚀皮肤，类别1A，1B，1C
严重眼损伤，类别1
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
对水环境的危害
急性危害，类别1
慢性危害，类别1,2
欧盟危险性物质标志
爆炸性 (E)
环境危害性 (N)
有害性 (Xn)MSDS下载
个人保护装置
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS警示性声明
P273-P280-P305+P351+P338
安全公开号
36/37-61
联合国危险货物编号
2923
联合国危险货物等级
8
GHS危险声明
H290-H302-H312-H315-H317-H319-H351-H373-H400
危险公开号
2-21/22-36/38-40-43-48/22-50
RTECS编号
NC3675000
GHS警示词
Warning
RID/ADR
UN 2923 8/PG 2
联合国危险货物包装类别(PG)
2
德国WGK号
3
产品相关信息
杂质
≤0.005% S compounds
<10 ppm total metallic impurities
≤0.25 meq/g Titr. free acid
痕量阳离子
heavy metals: ≤5 ppm
Fe: ≤5 ppm
NH4+:, passes test
线性分子式
NH2OH · HCl
燃烧残渣
≤0.05%
纯度
99.999% trace metals basis
理化性质
熔点
155-157 °C (dec.)(lit.)
密度
1.67 g/mL at 25 °C(lit.)
描述信息
Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
Features and Benefits
符合 A.C.S. 的试剂规范。
包装
50, 250 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2a receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8
MAO 抑制剂;抑制血小板聚集。
Features and Benefits
符合 A.C.S. 的试剂规范。
包装
50, 250 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2a receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8
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